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Sales Manager Job (Ballerup, DK)

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Sales Manager-SAL003287

Description

Today MSD is working to help the world be well. Through our prescription medicines, vaccines, biological therapies, consumer care and animal health products and services, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them.

About MSD in Denmark

We are a significant provider to the Danish health service and supply more than 90 different treatments for a wide range of therapeutic areas, and we are the global pharmaceutical company, that invests the most in clinical research in Denmark. We employ approximately 200 highly qualified employees that work within sales, marketing and clinical research and policy/medical affairs in 3 divisions: Global Human Health, Merck Research Laboratories and Animal Health.

Human Health Denmark

We make products that touch the lives of millions on a global scale. That’s the reason we come to work every day. Our human health portfolio includes healthcare solutions and innovative treatment in areas such as heart disease, diabetes, arthritis, allergies, HIV, Hepatitis C, ophthalmology, asthma, osteoporosis and gastroenterology. We have a long heritage in the development of vaccines.

When it comes to solving healthcare problems of the future, our portfolio is supported by a robust pipeline, with a range of products in each phase of development. That is how we help bring about a healthier world – one in which we all do our part to make what’s possible, real.

Sales Manager

The Sales Manager is reporting directly to the Business Unit Director and is responsible for Sales Management. This includes recruitment and selection, training and development, supervision and coaching of an assigned Field Sales Force. The Sales Manager is responsible for managing his/her Sales Team by ensuring high quality performance and successful implementation of marketing plans, in order to achieve all approved sales objectives of assigned MSD promoted products. As such, it is upon the Sales Manager to spend the majority of his/her time in the field with his/her team. The Sales Manager works within the ethical standards of the company.

Manage the lead product and sales:

- Ensure that sales targets for the lead product are achieved or exceeded by developing sales implementation plans in line with the approved marketing strategy and managing the flawless execution of those plans within the approved expense budgets
- Monitor execution of district activity plans by reviewing key metrics through MSD's CRM system on a monthly basis and adjust plans as appropriate
- Secure time management in line with key priorities (65% field activities) and monitor through MSD's CRM system on a monthly basis

Manage the business:

- Ensure that sales team delivers all approved activities for the lead product, co-promotion of the second product and reminder calls of the third product, in line with approved marketing strategies and within approved expense budgets
- Maintain proper coordination with other Brand & Customer Managers to ensure that implementation of all field operations are properly conducted for customers’ benefits
- Secure implementation of district activity plans for all products assigned to the Sales Team
- Monitor all activities to achieve desired outcomes
- Manage regional scientific leaders for the lead product
- Always look for ways to improve our go to market model.

Manage the sales team:

- Ensure proper headcount planning to minimize vacant territories
- Ensure adequately staffed sales team with motivated and qualified employees by selecting, coaching, developing, rewarding and retaining the right people
- Lead and inspire the sales team to ensure high individual and team performance
- Ensure that the Performance Management Process (PMP) will be taken care of professionally

Demonstrate Merck Leadership Standards:

- Responsible for maintaining and improving high ethical perception of MSD attitude towards employees, colleagues, customers and all stakeholders
- Ensure that business is conducted according to Merck Policies and Procedures, and Standards and Values
- Ensure that communication between reps and the MSD organization is efficient, timely and accurate
- Be sensitive to the inherent responsibility of representing the company at district level
- Participate in special projects on an ad-hoc basis

Pharmaceuticals that have changed the world

Since MSD was founded in the late 18th century, the company has developed pharmaceuticals with a great impact on the global public health.

Penicillin: In the late 1930’s, MSD started doing research in antibiotics. The first

penicillin treatment was available from MSD’s laboratories in the USA in 1942.

Vaccines: In earlier days, no preventive treatment were available against diseases

such as measles, mumps, varicella (chickenpox) and rubella. MSD is behind severalof the vaccines that are part of vaccination programs all over the world today.

HIV/AIDS: In 1996, MSD launched a protease-antagonist, Crixivan, for the treatment of HIV/AIDS. Today, this remains one of the most complex pharmaceuticals ever developed by chemical synthesis..Statins: In 1987, MSD launched the World’s first statin, Meyacor. Today, statins is the most widely used group of pharmaceuticals to lower cholesterol.

Osteoporosis: In 1996, MSD launched Fosamax – a new treatment in a new class of pharmaceuticals against osteoporosis which prevents bone deterioration.

A good place to work

If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Qualifications

Background:

- Master's degree preferred
- Solid track record from other people management role

Skills Required:

- High level knowledge of and experience in the pharmaceutical business environment and products and disease areas covered by the company
- Superior people management skills
- Superior planning skills
- Good communication skills (oral/written), fluent in Danish and English
- IT usage ability
- Good analytical skills
- Extensive selling experience
- Good negotiation skills
*LI-LVG1

Job: Sales Animal MAH

Job Title: Sales Manager

Primary Location: EMEA-DK-84-Ballerup

Employee Status: Regular

Number of Openings: 1

Senior Sales Representative, Primary Care Job (Ballerup, DK)

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Senior Sales Representative, Primary Care-SAL003121

Description

About MSD

Today’s MSD is working to help the world be well. Through our prescription medicines, vaccines, biological therapies, and consumer care and animal health products and services, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. For more information, visit our website. http://www.msd.dk/

About MSD in Denmark

We are a significant provider to the Danish health service and supply more than 90 different treatments for a wide range of therapeutic areas, and we are the global pharmaceutical company, that invests the most in clinical research in Denmark. We employ approximately 200 highly qualified employees that work within sales, marketing and clinical research and policy/medical affairs in 3 divisions: Global Human Health, Merck Research Laboratories and Animal Health. In a time where many international businesses move their activities to other Scandinavian locations, MSD has chosen to consolidate its Mid-European activities in Denmark. MSD offices in Ballerup, Copenhagen, are the base for MSD’s Mid-Europe 2 regional headquarters which count approximately 1,600 employees in 10 countries (Denmark, Iceland, Sweden, Norway, Finland, Switzerland, Austria, Latvia, Estonia and Lithuania). The region runs clinical studies involving approximately 30,000 patients and investments in research and development amount to nearly 90 million dollars US dollars annually.

Human Health Denmark

We make products that touch the lives of millions on a global scale. That’s the reason we come to work every day. Our human health portfolio includes healthcare solutions and innovative treatment in areas such as heart disease, diabetes, arthritis, allergies, HIV, Hepatitis C, ophthalmology, asthma, osteoporosis and gastroenterology. We have a long heritage in the development of vaccines and when it comes to solving healthcare problems of the future, our portfolio is supported by a robust pipeline, with a range of products in each phase of development. That is how we help bring about a healthier world – one in which we all do our part to make what’s possible, real.

Position Overview:

As a sales representative, you get an interesting and varied job with exciting challenges. You are responsible for planning, prioritizing, and implementing sales activities for our primary customers - the primary care physicians (general practitioners). In addition to planning and implementing individual meetings and group meetings in primary care physician offices, your responsibilities will be planning and implementing local meetings in districts and participation in symposia, conferences and congresses both in Denmark and abroad. You are part of a dynamic and innovative team, and you are responsible for achieving sales targets in the Copenhagen territory for assigned MSD promoted products with a current focus on products within the atherosclerosis and diabetes franchises.

As a sales representative you are required to work with the territory team and other MSD personnel to develop and implement district activity plans and meeting customer needs. You are also required to actively utilize new multichannel communication methods and activities. The sales representative works within the ethical standards of the company and the legal regulations in the country.

Roles & Responsibilities:

Responsible for own territory business (revenue and income).

Responsible for understanding and fulfilling own customer’s needs which are in line with business priorities and needs.

Responsible for planning and implementing optimal activities to achieve targets.

Responsible for arranging individual meetings, educational meetings and symposia in primary care physician offices, health centers, and other venues for physicians and other HCP’s.

To work effectively in co-operation with both office based MSD colleagues and colleagues working at the same territory.

Create additional value and solutions to customers and build trust.

Utilization of wide range of communication channels to serve customer needs.
Utilization of CRM system for effective planning and prioritization of selling activities based on own territory data analysis.

Qualifications

Educational background and Experience:

Health Care Professional and/or business degree.

Experience from the pharmaceutical industry and/or medical device industry.

Personal qualifications

Business oriented and has entrepreneurial mindset;

Ability and willingness to use CRM system effectively;

Prudent risk taking;

Strong analytic thinking skills which leads to especially in segmentation, targeting and tracking;

Excellent communication skills;

Teamwork oriented with leadership skills;

Solution and goal oriented;

Fluent in Danish & English;

Skills to establish trusted long term customer relationships and networks, understanding of customer needs and readiness to implement appropriate actions

Good computing skills and ability to learn new IT solutions;

Ability and willingness to use new multichannel communication solution resources effectively to meet customer needs;

New kind of thinking, able to find hiding business, ability to think how to use the available tools to provide individual physicians with more value;

Ability to prioritize and focus work according to business opportunities.

A good place to work

If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Our pharmaceuticals that have changed the world

Since MSD was founded in the late 18th century, the company has developed pharmaceuticals with a great impact on the global public health.

Penicillin: In the late 1930’s, MSD started doing research in antibiotics. The first penicillin treatment was available from MSD’s laboratories in the USA in 1942.

Vaccines: In earlier days, no preventive treatments were available against diseases such as measles, mumps, varicella (chickenpox) and rubella. MSD is behind several of the vaccines that are part of vaccination programs all over the world today.

HIV/AIDS: In 1996, MSD launched a protease-antagonist, Crixivan, for the treatment of HIV/AIDS. Today, this remains one of the most complex pharmaceuticals ever developed by chemical synthesis.

Statins: In 1987, MSD launched the World’s first statin, Meyacor. Today, statins is the most widely used group of pharmaceuticals to lower cholesterol.

Osteoporosis: In 1996, MSD launched Fosamax – a new treatment in a new class of pharmaceuticals against osteoporosis which prevents bone deterioration.

*LI-LVG1

Job: Sales

Job Title: Senior Sales Representative, Primary Care

Primary Location: EMEA-DK-84-Ballerup

Employee Status: Regular

Number of Openings: 1

Senior Sales Representative, Primary Care Job (Ballerup, 84, DK)

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Senior Sales Representative, Primary Care-SAL003121

Description

About MSD

Today’s MSD is working to help the world be well. Through our prescription medicines, vaccines, biological therapies, and consumer care and animal health products and services, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. For more information, visit our website. http://www.msd.dk/

About MSD in Denmark

We are a significant provider to the Danish health service and supply more than 90 different treatments for a wide range of therapeutic areas, and we are the global pharmaceutical company, that invests the most in clinical research in Denmark. We employ approximately 200 highly qualified employees that work within sales, marketing and clinical research and policy/medical affairs in 3 divisions: Global Human Health, Merck Research Laboratories and Animal Health. In a time where many international businesses move their activities to other Scandinavian locations, MSD has chosen to consolidate its Mid-European activities in Denmark. MSD offices in Ballerup, Copenhagen, are the base for MSD’s Mid-Europe 2 regional headquarters which count approximately 1,600 employees in 10 countries (Denmark, Iceland, Sweden, Norway, Finland, Switzerland, Austria, Latvia, Estonia and Lithuania). The region runs clinical studies involving approximately 30,000 patients and investments in research and development amount to nearly 90 million dollars US dollars annually.

Human Health Denmark

We make products that touch the lives of millions on a global scale. That’s the reason we come to work every day. Our human health portfolio includes healthcare solutions and innovative treatment in areas such as heart disease, diabetes, arthritis, allergies, HIV, Hepatitis C, ophthalmology, asthma, osteoporosis and gastroenterology. We have a long heritage in the development of vaccines and when it comes to solving healthcare problems of the future, our portfolio is supported by a robust pipeline, with a range of products in each phase of development. That is how we help bring about a healthier world – one in which we all do our part to make what’s possible, real.

Position Overview:

As a sales representative, you get an interesting and varied job with exciting challenges. You are responsible for planning, prioritizing, and implementing sales activities for our primary customers - the primary care physicians (general practitioners). In addition to planning and implementing individual meetings and group meetings in primary care physician offices, your responsibilities will be planning and implementing local meetings in districts and participation in symposia, conferences and congresses both in Denmark and abroad. You are part of a dynamic and innovative team, and you are responsible for achieving sales targets in the Copenhagen territory for assigned MSD promoted products with a current focus on products within the atherosclerosis and diabetes franchises.

As a sales representative you are required to work with the territory team and other MSD personnel to develop and implement district activity plans and meeting customer needs. You are also required to actively utilize new multichannel communication methods and activities. The sales representative works within the ethical standards of the company and the legal regulations in the country.

Roles & Responsibilities:

Responsible for own territory business (revenue and income).

Responsible for understanding and fulfilling own customer’s needs which are in line with business priorities and needs.

Responsible for planning and implementing optimal activities to achieve targets.

Responsible for arranging individual meetings, educational meetings and symposia in primary care physician offices, health centers, and other venues for physicians and other HCP’s.

To work effectively in co-operation with both office based MSD colleagues and colleagues working at the same territory.

Create additional value and solutions to customers and build trust.

Utilization of wide range of communication channels to serve customer needs.
Utilization of CRM system for effective planning and prioritization of selling activities based on own territory data analysis.

Qualifications

Educational background and Experience:

Health Care Professional and/or business degree.

Experience from the pharmaceutical industry and/or medical device industry.

Personal qualifications

Business oriented and has entrepreneurial mindset;

Ability and willingness to use CRM system effectively;

Prudent risk taking;

Strong analytic thinking skills which leads to especially in segmentation, targeting and tracking;

Excellent communication skills;

Teamwork oriented with leadership skills;

Solution and goal oriented;

Fluent in Danish & English;

Skills to establish trusted long term customer relationships and networks, understanding of customer needs and readiness to implement appropriate actions

Good computing skills and ability to learn new IT solutions;

Ability and willingness to use new multichannel communication solution resources effectively to meet customer needs;

New kind of thinking, able to find hiding business, ability to think how to use the available tools to provide individual physicians with more value;

Ability to prioritize and focus work according to business opportunities.

A good place to work

If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Our pharmaceuticals that have changed the world

Since MSD was founded in the late 18th century, the company has developed pharmaceuticals with a great impact on the global public health.

Penicillin: In the late 1930’s, MSD started doing research in antibiotics. The first penicillin treatment was available from MSD’s laboratories in the USA in 1942.

Vaccines: In earlier days, no preventive treatments were available against diseases such as measles, mumps, varicella (chickenpox) and rubella. MSD is behind several of the vaccines that are part of vaccination programs all over the world today.

HIV/AIDS: In 1996, MSD launched a protease-antagonist, Crixivan, for the treatment of HIV/AIDS. Today, this remains one of the most complex pharmaceuticals ever developed by chemical synthesis.

Statins: In 1987, MSD launched the World’s first statin, Meyacor. Today, statins is the most widely used group of pharmaceuticals to lower cholesterol.

Osteoporosis: In 1996, MSD launched Fosamax – a new treatment in a new class of pharmaceuticals against osteoporosis which prevents bone deterioration.

*LI-LVG1

Job: Sales

Job Title: Senior Sales Representative, Primary Care

Primary Location: EMEA-DK-84-Ballerup

Employee Status: Regular

Number of Openings: 1

Technical Manager Pluimvee Job (Boxmeer, NB, NL)

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Technical Manager Pluimvee-SCI004031

Omschrijving
MSD Animal Health ontwikkelt en produceert vaccins en farmaceutische producten voor dieren. Met kantoren in meer dan 50 landen en producten in meer dan 140 markten maken wij deel uit van het wereldwijde MSD netwerk van Research & Development en productie locaties. MSD Animal Health zoekt altijd innovatief talent dat wil bijdragen aan de verdere ontwikkeling van onze markten, producten en werkwijzen. Voor meer informatie verwijzen we je graag http://www.msd-animal-health.nl/

MSD Animal Health Nederland is met ongeveer 45 medewerkers verantwoordelijk voor de marketing, verkoop, distributie en ondersteuning van de producten van MSD Animal Health. Ter versterking van het team Pluimvee zoekt MSD Animal Health Nederland op dit moment een:

Technical Manager Pluimvee

MSD Animal Health is marktleider en biedt aan de Nederlandse dierenarts een breed portfolio in combinatie met deskundig advies en een uitstekende service. De verkoopactiviteiten zijn gerangschikt in vier business units: gezelschapsdieren, herkauwers, pluimvee en varkens.

In de business unit pluimvee werk je nauw samen met de account manager en de business unit manager. Als Technical Manager Pluimvee werk je met lokale en internationale collegae aan het leveren van kennis voor de pluimveesector. Gebaseerd op jouw praktijkervaring als pluimveedierenarts vertaal je veterinaire vraagstukken naar oplossingen binnen het MSD portfolio die passen bij de behoeften en mogelijkheden van klanten (dierenartsen, pluimveehouders, broederijen, fokorganisaties,, onderzoekers en overheidsfunctionarissen). Daarnaast onderzoek je pro actief mogelijkheden om de toepassing en afzet van MSD producten te bevorderen. Vanuit je technische kennis ondersteun je het verkoopproces. Je rapporteert aan de Business Unit Manager Pluimvee.

Als Technical Manager ben je verantwoordelijk voor:

- Het technisch adviseren inzake het gebruik van MSD Pluimvee medicijnen en vaccins.
- Samen met Account manager bezoek je op gerichte wijze de dierenartsen.
- Als Technical Manager Manager Pluimvee ben je een volwaardig technisch gesprekspartner, die naast het brede MSD producten pakket ook meedenkt over bredere technische marktontwikkelingen binnen de pluimvee sector.
- Je houdt presentaties voor dierenartsenpraktijken en pluimveehouders en onderhoudt contact met opinieleiders.
- Je hebt of ontwikkelt een uitgebreid netwerk in de periferie van de Nederlandse pluimveehouderij (denk aan voerfabrikanten, broederijen en fokorganisaties).
- Je initieert en begeleidt de uitvoering en uitwerking van praktijkproeven.

Kwalificaties
- Afgestudeerd dierenarts (bij voorkeur met specialisatie Pluimvee).
- Ten minste vijf jaar relevante bedrijfservaring als praktiserend pluimvee dierenarts.
- Goede kennis van en visie op ontwikkeling van de pluimvee sector.
- Je kunt verkoopbudgetten en doelstellingen realiseren.
- Je bent een ondernemende en collegiale teamplayer die creativiteit en innovatie als kernwaarden heeft.
- Een pro-actieve en innovatieve instelling om de MSD producten aan te laten sluiten met de behoeften in de markt.
- Naast een primair technisch-wetenschappelijk oriëntatie beschik je over duidelijk voeling met de commerciële aspecten van de pluimveehouderij.

Voor vragen omtrent deze vacature kan je je wenden tot Frank Bekkers, BU Manager Pluimvee te bereiken op +31 485 58 7650. Voor vragen omtrent het selectieprocedure kan je je wenden tot Koen Roozen, Recruiter via koen.roozen@merck.com. Solliciteren bij voorkeur via de sollicitatiebutton.

- LI-KR1
Functie: Scientific Marketing Affairs
Job Title: Veterinary Service Manager Poultry

Primaire locatie: EMEA-NL-NB-Boxmeer
Status van medewerker: Vast
Aantal vacatures: 1

Pharmacovigilance Country Lead Job (Ballerup, DK)

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Pharmacovigilance Country Lead-REG001204

Description

About MSD

Today’s MSD is working to help the world be well. Through our prescription medicines, vaccines, biological therapies, and consumer care and animal health products and services, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. For more information, visit our website. http://www.msd.dk/

About MSD in Denmark

We are a significant provider to the Danish health service and supply more than 90 different treatments for a wide range of therapeutic areas, and we are the global pharmaceutical company, that invests the most in clinical research in Denmark. We employ approximately 200 highly qualified employees that work within sales, marketing and clinical research and policy/medical affairs in 3 divisions: Global Human Health, Merck Research Laboratories and Animal Health.

Human Health in Denmark

We make products that touch the lives of millions on a global scale. That’s the reason we come to work every day. Our human health portfolio includes healthcare solutions and innovative treatment in areas such as heart disease, diabetes, arthritis, allergies, HIV, Hepatitis C, ophthalmology, asthma, osteoporosis and gastroenterology. We have a long heritage in the development of vaccines and when it comes to solving healthcare problems of the future, our portfolio is supported by a robust pipeline, with a range of products in each phase of development. That is how we help bring about a healthier world – one in which we all do our part to make what’s possible, real.

For our Pharmacovigilance Department in Ballerup we are currently recruiting a: Pharmacovigilance Country Lead.

The position

As a Pharmacovigilance (PV) Country Lead you will be responsible for overseeing and managing the day-to-day activities of the Pharmacovigilance Department at MSD Denmark. You will be responsible for:

..

· Ensuring compliance with PV processes and regulations, and Merck policies and procedures

· Supervising two pharmacovigilance colleagues;

· Taking responsibility as a people manager for recruitment, training, development and performance management;

· Representing MSD for any local safety issues, interfacing with colleagues from different functional areas, e.g. local Clinical Trial Operations, Regulatory Affairs department, to ensure alignment on issues impacting PV.

You will report into the Global Safety Regional Leader, who is located in Norway.

Qualifications

The candidate

· Master’s/ Bachelor’s degree in health, life science, medical science, regulatory affairs or equivalent by experience;

· At least three years of people management experience in a pharmaceutical environment;

· At least three years of industry experience in pharmacovigilance or regulatory affairs;

· Extensive knowledge of pharmacovigilance regulations in Denmark;

· Strong leadership, communication, social and problem-solving skills;

· Demonstrated ability to build and manage close relationships with local key health authorities;

· Experience interacting with auditors/ inspectors and conducting qualifications audits (a plus);

· Experience with MS-Office and preferably with other IT-applications;

· Proficiency in English and Danish language (written and oral).

Information

Questions and further information regarding the position can be addressed to Guri Schüller, Regional PV Lead Scandinavia & Mid Europe MSD (Norway) AS, tel: +47 32 20 74 28 or via

e-mail (guri_schuller@merck.com).

Application

If you are interested in this challenging role, you are invited to apply online by uploading your resume and application letter in English.

A good place to work

If you enjoy being challenged over and over again, but also to have fun and a good team spirit and cooperation, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Our pharmaceuticals that have changed the world

Since MSD was founded in the late 18th century, the company has developed pharmaceuticals with a great impact on the global public health:

Penicillin: In the late 1930’s, MSD started doing research in antibiotics. The first penicillin treatment was available from MSD’s laboratories in the USA in 1942.

Vaccines: In earlier days, no preventive treatments were available against diseases such as measles, mumps, varicella (chickenpox) and rubella. MSD is behind several of the vaccines that are part of vaccination programs all over the world today.

HIV/AIDS: In 1996, MSD launched a protease-antagonist, Crixivan, for the treatment of HIV/AIDS. Today, this remains one of the most complex pharmaceuticals ever developed by chemical synthesis.

Statins: In 1987, MSD launched the World’s first statin, Meyacor. Today, statins is the most widely used group of pharmaceuticals to lower cholesterol.

Osteoporosis: In 1996, MSD launched Fosamax – a new treatment in a new class of pharmaceuticals against osteoporosis which prevents bone deterioration.

*LI-RS1

Job: Regulatory Affairs Generic

Job Title: Pharmacovigilance Country Lead

Primary Location: EMEA-DK-84-Ballerup

Employee Status: Regular

Travel: No

Number of Openings: 1

Therapy Manager - Kolkata (Critical Care) Job (Kolkata, IN)

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Therapy Manager - Kolkata (Critical Care)-DIR005747

Description

Product Promotion:
- Drive opening of new business avenues for Respiratory in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the Respiratory product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the Respiratory Products in the pharmacopoeia

Territory Sales:
- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the cc products.
- To maintain and balance right distribution of products to the Pharmacy.

Market Intelligence/ Sales Reporting
-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

Demand Generation and Stock Liquidation:
- Develop relationships with heads of departments in the hospital and influence them to drive liquidation of MSD stock and seek recommendations for MSD products
- Coordinate with KAM and purchase officer to generate demand for MSD products
- Coordinate with stockists for order execution

Customer Relationship Management:
- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

B Pharm / BSc

Job: Direct Sales -Nondurable Goods

Job Title: Customer Representative

Primary Location: APAC-IN-WB-Kolkata

Employee Status: Regular

Number of Openings: 1

Shift (if applicable): N/A

Senior Account Manager Gezelschapsdieren Job (Direct Sales Generic MAH)

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Senior Account Manager Gezelschapsdieren-DIR005466

Omschrijving
MSD Animal Health ontwikkelt en produceert vaccins en farmaceutische producten voor dieren. Met kantoren in meer dan 50 landen en producten in meer dan 140 markten maken wij deel uit van het wereldwijde MSD netwerk van Research & Development en productie locaties. MSD Animal Health zoekt altijd innovatief talent dat wil bijdragen aan de verdere ontwikkeling van onze producten en werkwijzen. Voor meer informatie verwijzen we je graag http://www.msd-animal-health.nl/

MSD Animal Health Nederland is met ongeveer 45 medewerkers verantwoordelijk voor de marketing, verkoop, distributie en ondersteuning van de producten van MSD Animal Health.

Ter versterking van het Gezelschapsdierenteam zoekt MSD Animal Health Nederland op dit moment een:

Senior Account Manager

MSD Animal Health is marktleider en biedt aan de Nederlandse dierenarts een breed portfolio in combinatie met deskundig advies en een uitstekende service. De verkoopactiviteiten zijn gerangschikt in vier business units: gezelschapsdieren, herkauwers, pluimvee en varkens.

De business unit ‘Gezelschapsdieren’ telt elf enthousiaste collega’s waaronder vijf account managers. Binnen het team wordt nauw samengewerkt tussen account managers, productmanagers en technical managers.

Als Account Manager ben je verantwoordelijk voor:

- de verkoop van producten voor gezelschapsdieren
- via een systematische en gedifferentieerde klantbenadering ontwikkel je relaties met dierenartsen en informeert ze over ontwikkelingen op veterinair gebied.
- Je adviseert dierenartsen over de inzet van vaccins, farmaceutische producten en serviceconcepten in de dierenartsenpraktijk.
- Als Account Manager ben je een volwaardige gesprekspartner die naast productadvisering ook over bedrijfseconomische en –technische marktontwikkelingen kan meepraten.
- Je bezoekt op gerichte wijze de dierenartsen (in het bijzonder grotere accounts) en bepaalt samen met de Productmanager promotionele en service activiteiten

Je werkt zelfstandig vanuit huis en zorgt voor een accurate bezoek- en verkoopadministratie. Vanzelfsprekend onderhoud je nauw contact met je collega's op kantoor.

Kwalificaties
- Een proactieve collega met een zelfstandige houding die op juiste wijze kan omgaan met veel bewegingsvrijheid.
- Een afgeronde HBO opleiding (bijv. in Commerciële Economie, HAS, Bedrijfskunde)
- Gedegen kennis van marketing en accountmanagement.
- In staat om korte en lange termijn acties te plannen op basis van analyse en toekomstvisie
- Minimaal drie jaar relevante commerciële buitendienst ervaring
- Een goede kennis van de veterinaire markt.
- Kennis van of affiniteit met de gezelschapsdierensector (hond & kat);
- Netwerker met zowel interne- als externe contacten
- Woonachtig in het midden van Nederland
Functie: Direct Sales Generic MAH
Job Title: Senior Customer Representative

Primaire locatie: EMEA-Nederland
Status van medewerker: Vast
Aantal vacatures: 1

Manager Global CMC Regulatory Affairs - Supply Job (EMEA-Netherlands)

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Manager Global CMC Regulatory Affairs - Supply-REG001119

Description

For our location in Oss (The Netherlands) we are currently recruiting a:

Manager Global CMC Regulatory Affairs - Supply

About MSD

MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies, consumer care and animal health products, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD has a workforce of over 6.000 in the Netherlands at five different sites. For more information, visit our website www.msd.nl or www.msd-animal-health.nl/

The position

MSD has a challenging opening for a candidate who not only can demonstrate CMC regulatory expertise, but also management capability. The successful candidate will lead a team located in Oss (The Netherlands) that currently encompasses 8 staff members and 2 contractors responsible for the maintenance of existing chemical and pharmaceutical manufacturing and controls (CMC) worldwide registrations. This is done through:

·

* Supervising/ coordinating/ preparing/reviewing the chemistry, manufacturing, and controls information for worldwide marketing of pharmaceutical products (NDA, WMA, MAA) to include annual reports, registration renewals, supplements, variations and responses;

* · Defining the strategy for filing post approval changes, responding to agency or subsidiary questions;

* · Prioritizing workload for the team;

* · Resolving issues;

* · Corresponding continuously and interacting with regulatory agencies and other Merck scientists to support in-line product filings worldwide;

* · Maintaining a working knowledge of current governmental and worldwide requirements for re-registration and post-approval changes;

* · Assuring that that filed information on the current manufacturing and testing procedures is kept updated for each product using appropriate departmental systems;

* · Ensuring consistency in practices, championing best practices and promoting operational excellence;

* · Partnering with others in the pharmaceutical industry and regulators to reduce the regulatory burden of making post approval improvements in CMC;

* · Identifying initiatives to promote Operational Excellence;

* · Supporting new and existing CMC systems (RCAM, ORION, QSIS) and assuring compliance with those systems;

* · Supporting staffing needs, training, promoting growth through new opportunities and understanding of each person's Employee Development Plan;

* · Identifying and promoting best practices within CMC;

* · Maintaining superior knowledge of current government regulations and worldwide requirements for initial registration, re-registration and post-approval changes;

* · Demonstrating leadership in departmental improvement activities such as system modifications, maintenance of standard operating procedures, internal guidelines, etcetera;

* · Participating in external discussion groups, societies, working groups to influence market requirements, promoting harmonization, and reducing the regulatory burden;

* · Identifying internal and external customer needs and leading the team in accordance with those needs.

Qualifications

The candidate

* · Degree in pharmacy, bio-pharmaceutics, analytical chemistry, organic chemistry, chemical engineering or a related discipline;

* · At least ten years of industrial experience in chemical/ pharmaceutical research or manufacturing including processing and/ or analytical testing;

* · Working knowledge in quality assurance and quality systems (a plus);

* · Significant knowledge of regulations related to CMC;

* · Able to manage projects to achieve high productivity, prioritizing, and managing effective meetings;

* · Effective leadership;

* · Providing strategic direction and facilitating changes needed to move in that direction;

* · Innovative, flexible and collaborative;

* · Demonstrated problem solving and decision making skills;

* · Positive vision for the future of Merck/ MSD;

* · Awareness of Merck’s/ MSD’s overall business objectives and strategies;

* · Working knowledge of Word, Excel, PowerPoint and Document Management Systems;

* · Superior oral and written communication skills in English, Dutch and/or other languages are preferred.

A good place to work

MSD is an attractive employer offering interesting opportunities in Research & Development, production and staff departments for an enormous range of disciplines such as biologists, chemists, process engineers, technicians, mechatronic engineers, pharmacists and operators. MSD always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD values and rewards most. If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Information

For more information about the vacancy, please contact Tom Sam, Head Global CMC Regulatory Affairs, by phone: +31 6 101 837 60 or via e-mail tom.sam@merck.com.

Application

If you are interested in this position, you are invited to apply online.

Job: Regulatory Affairs - CMC

Job Title: Manager Global CMC Regulatory Affairs - Supply

Primary Location: EMEA-Netherlands

Employee Status: Regular

Number of Openings: 1

Improvement Engineer MSD Animal Health Job (Boxmeer, NL)

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Improvement Engineer MSD Animal Health-MAI000296

Description

The primary purpose of the position is to support the IPT, to identify improvement opportunities and lead the execution of plans which are prioritized to the business objectives. As an Improvement Engineer you are an expert in Lean Six Sigma methods and you will support improvement initiatives within one of the IPT’s. This involves development and transfer of LSS knowledge, structural problem solving and process robustness and –efficiency initiatives in production or planning & logistics. Also collaboration with peers in the site and other sites of the MSD network is an important part of the job. As an Improvement Engineer you will report to the Improvement Lead.

Within a multidisciplinary pharmaceutical production environment the main field of your attention is:

- Support of business improvement initiatives.
- Contribute to the deployment of the MSD Production System.
- Develop and transfer knowledge of Lean Six Sigma and Inclusion.
- Identify, analyze and prioritize improvements for technical or business related processes, systems and behaviors.
- Implement and maintain the improvement project portfolio to support the IPT from a business perspective.
- Support investigations on problems/deviations including defining corrective and preventive actions.
- Contribute to a data driven decision making process.
- Assure effective application of Lean Six Sigma methods by leading projects, facilitating Kaizens and coaching sponsors and practitioners.

Qualifications

- Bachelor's degree (Biotechnology/Food technology, Operations Management, Planning & Logistics is preferred).
- At least 5 years of relevant work experience of which at least 2 year in an improvement or change agent role (preferably in a regulated environment e.g. Pharmacy, Chemistry or Food).
- Strong change management skills.
- Experienced in project management.
- A Certified Green Belt / Black belt with hands on experience with application of most of the following Lean and Six Sigma tools and techniques like Structured Problem Solving, Visual Factory/Management, A3, Value Stream Mapping, Kaizen facilitation, 5S, etc.
- Experience in training, coaching and guidance of people in correct use of LSS principles.
- Ongoing focus on identification and realization of improvement potential.
- Result driven team player.
- “An energetic, enthusiastic motivator”
- Excellent oral and written skills in English and Dutch.

A good place to work

MSD Animal Health always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD Animal Health has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD Animal Health values and rewards most.

For information about this vacancy please contact Koen Roozen (Recruiter) at +31 (0)6 2141 9206 or koen.roozen@merck.com. Closing date for applications is 25-04-2013.

Job: Manufacturing Engineering

Job Title: Improvement Engineer

Primary Location: EMEA-NL-NB-Boxmeer

Employee Status: Regular

Number of Openings: 5

Shift (if applicable): N/A

Therapy Manager (Respiratory- Ahmedabad) Job (Ahmedabad, IN)

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Therapy Manager (Respiratory- Ahmedabad)-SAL003317

Description

Product Promotion:
- Drive opening of new business avenues for Respiratory & Derma in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the Respiratory & Derma product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the Respiratory & Derma Products in the pharmacopoeia

Territory Sales:
- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the Respiratory & Derma products.
- To maintain and balance right distribution of products to the Pharmacy.

Market Intelligence/ Sales Reporting
-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

Demand Generation and Stock Liquidation:
- Develop relationships with heads of departments in the hospital and influence them to drive liquidation of MSD stock and seek recommendations for MSD products
- Coordinate with KAM and purchase officer to generate demand for MSD products
- Coordinate with stockists for order execution

Customer Relationship Management:
- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

B Pharm / BSc

Job: Sales

Job Title: Customer Representative

Primary Location: APAC-IN-GJ-Ahmedabad

Employee Status: Regular

Number of Openings: 1

Shift (if applicable): N/A

Therapy Manager - Mumbai (Hepatitis) Job (Mumbai, IN)

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Therapy Manager - Mumbai (Hepatitis)-SAL003316

Description

Product Promotion:
- Drive opening of new business avenues for Hepatitis in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the Hepatitis product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the Hepatitis Products in the pharmacopoeia

Territory Sales:
- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the Hepatitis products.
- To maintain and balance right distribution of products to the Pharmacy.

Market Intelligence/ Sales Reporting
-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

Demand Generation and Stock Liquidation:
- Develop relationships with heads of departments in the hospital and influence them to drive liquidation of MSD stock and seek recommendations for MSD products
- Coordinate with KAM and purchase officer to generate demand for MSD products
- Coordinate with stockists for order execution

Customer Relationship Management:
- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

B Pharm / BSc

Job: Sales

Job Title: Customer Representative

Primary Location: APAC-IN-MH-Mumbai

Employee Status: Regular

Number of Openings: 2

Shift (if applicable): N/A

Product Specialist - Hospital & Speciality Job (EMEA-Egypt-Alexandria)

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Product Specialist - Hospital & Speciality-CHA000286

Description

Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of people like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.


Merck is known as MSD outside of the United States and Canada

Closing date 28th March

Monitor, focus and maximize the potential key account customers and key opinion leaders

Recommend preliminary target forecast, breakdown of sales, planned activities and objectives to ensure achieving sales target on a monthly basis.

Search and identify new leading customers per market segment.

Prepare daily, weekly and monthly reports and/or plans.

Prepare weekly marketing activities) e.g. group meetings, sponsorship of local or international events.)

Follow up on proper storage and distribution of products.

Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

Qualifications

· Pharmacy , Medicine, Veterinary, or Dentistry Graduate

· Minimum 2 years’ experience as a CR

· Results oriented with ability to meet deadlines and handle challenging assignments

· Very Good command of English language

· Very good in Computer skills.

· Competent presentation skills.

· Self-motivated and energetic with drive to excel

Willingness to travel within Egypt

Job: Channel Sales -Nondurble Goods

Job Title: Product Specialist - Hospital & Speciality

Primary Location: EMEA-Egypt-Alexandria

Employee Status: Regular

Number of Openings: 1

Therapy Manager (Derma - Delhi) Job (APAC-IN-Delhi)

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Therapy Manager (Derma - Delhi)-DIR005761

Description

Product Promotion:
- Drive opening of new business avenues for Respiratory & Derma in own territory hospitals through promotion of BU products to respective Medical fraternity in order to generate the business of the Respiratory & Derma product portfolio
- Use detail aids to support scientific selling and Liaison with the HOD's , Purchase committee and Drug Committee doctors at the institutions for inclusion of the Respiratory & Derma Products in the pharmacopoeia

Territory Sales:
- To prepare a target list of customers as per therapy profile. Understand and implement marketing strategies to medical fraternity to generate prescriptions for the cc products.
- To maintain and balance right distribution of products to the Pharmacy.

Market Intelligence/ Sales Reporting
-Interact with paramedical staff in hospitals to seek inputs on competitor activities, patients moving on MSD products, new products in the hospital etc. to maintain intelligence on MSD and competitor activity in the hospital
- Provide field reports in terms of FIRM, Tracker and Sales statement etc. in order to update the sales MIS

Demand Generation and Stock Liquidation:
- Develop relationships with heads of departments in the hospital and influence them to drive liquidation of MSD stock and seek recommendations for MSD products
- Coordinate with KAM and purchase officer to generate demand for MSD products
- Coordinate with stockists for order execution

Customer Relationship Management:
- Organizing and conducting CME's with the user department at the institution in coordination to create and build the market for MSD products
- Manage the relationship with KOL's. Build, maintain and grow new KBL's and support CRM-Scientific activities with KOL's

Qualifications

B Pharm / BSc

Job: Direct Sales -Nondurable Goods

Job Title: Customer Representative

Primary Location: APAC-IN-Delhi

Employee Status: Regular

Travel: Yes, 100 % of the Time

Number of Openings: 1

Shift (if applicable): N/A

Senior Manager Outcomes Research (m/w) Job (, ,)

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Senior Manager Outcomes Research (m/w)-MAR004440

Beschreibung

MSD gehört zu Merck & Co., Inc., mit Sitz in Whitehouse Station, N.J. (USA), einem global führenden Gesundheits-unternehmen. Mit seinen verschreibungspflichtigen Arzneimitteln, Impfstoffen, Biologika, Präparaten zur Selbstmedikation und für die Tiergesundheit in verschiedenen Therapiebereichen, bietet MSD in mehr als 140 Ländern umfassende und innovative Lösungen für Gesundheit.

Ein besonderes Anliegen von MSD ist darüber hinaus die Verbesserung der weltweiten Gesundheitsversorgung und der verbesserte Zugang zu Medikamenten. Dafür engagiert sich MSD in weitreichenden Gesundheitsprogrammen und Partnerschaften.

Zur Verstärkung unseres Market Access Teams suchen wir nach Uebereinkunft eine-/n

Outcomes Research Manager (m/w)

Ihr Aufgabenbereich umfassen im Einzelnen:

* Untersuchung des Nutzens und der Wirtschaftlichkeit unserer Produkte durch Initiierung,Durchführung, Publikation und Kommunikation entsprechenderOutcomes Research Studien in den Ihnen übertragenen Indikationsgebieten.

*
Erstellung von HTA-Berichten zu unseren Produkten im Rahmen von Nutzen- und Kostennutzenbewertungen und vertreten die Organisation auf wissenschaftlichen Kongressen und in Anhörungen des Instituts für Qualität und Wirtschaftlichkeit im Gesundheitswesen, des Gemeinsamen Bundesausschusses bzw. des GKV-Spitzenverbandes.

*
Enge Zusammenarbeit mit der Konzernzentrale, Auftragsforschungsinstituten, sowie wissenschaftlichen Meinungsbildnern

Qualifikationen

Sie passen zu uns, wenn Sie die folgenden Qualifikationen mitbringen:
* erfolgreich abgeschlossenes, vorzugsweise medizinisches Hochschulstudium, plus ggfs. Master of Public Health

* mehrjährige Erfahrung in der Planung und Interpretation von Studien zu Nutzen und Wirtschaftlichkeit von Arzneimitteln erste Berufserfahrung im Pharmabereich wünschenswert, aber nicht Voraussetzung

* Erfahrungenin klinischer Epidemiologie, evidenzbasierter Medizin, Gesundheitsökonomie bzw. Public Health

* Exzellente analytische Fähigkeiten

* hervorragender wissenschaftlicher Schreibstil

* Hohe Eigenmotivation

* Verhandlungssichere Englischkenntnisse

* Ausgeprägte kommunikative Fähigkeiten

Wir bieten Ihnen ein Arbeitsumfeld geprägt von vielen Möglichkeiten und klaren Grundsätzen an, sowie attraktive, soziale Leistungen und Flexibilität im Arbeitsalltag. Wir fördern Vielfalt und investieren gezielt in Nachwuchskräfte. Daher bieten wir Ihnen interessante Weiterentwicklungs– und Aufstiegsmöglichkeiten an. Falls Sie eine Laufbahn bei einem führenden, globalen Gesundheitsunternehmen suchen, dann würden wir uns freuen Sie als zukünftiges Talent in unserer Unternehmung entwickeln und fördern zu können.

Bitte bewerben Sie sich online auf: www.msd.de

Job: Marktforschung/-studie

Job Title
:Senior Manager Outcomes Research (m/w)

Primärer Standort: EMEA-Deutschland

Mitarbeiterstatus: Fest

Reisebereitschaft:: Ja, 10 % der Zeit

Anzahl offener Stellen: 2

Site Energy Lead Job (EMEA-Ireland)

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Site Energy Lead-ENG002460

Description

MSD Ireland (Ballydine) currently has a vacancy for a site Energy Lead. MSD Ireland (Ballydine) has a comprehensive energy management program in place and been successful in delivering significant energy reductions over recent years and plans to continue a program of aggressive energy reduction over the next number of years.

- Reporting to the Engineering & Facilities Management CoE Lead, the Energy Lead is responsible for leading the site energy management team and developing & managing the energy reduction programs on site. Specifically;
- Lead the site energy management team & ensure annual team objectives are developed and realized
- Develop energy reduction programs including energy kaizens, energy capital projects, energy treasure hunts and ongoing improvements such that there is full pipeline of opportunities and clear line of sight to energy reduction targets.
- Establish the annual energy consumption using a site model and planned energy reductions.
- Populate MSD energy trackers for forecasting & reporting for natural gas and electricity
- Energy Reporting to onsite leadership team, and local stakeholders
- Issue periodic energy reports (weekly & monthly) to monitor actual consumption patterns versus plan, identify variances and work with energy budget holders to investigate & remedy.
- Complete regular energy performance reviews with site leadership
- Continue to build energy sponsorship and improve visibility of energy consumption with budget holders
- Lead site energy awareness campaigns & initiatives
- Leverage energy best practices across the company and external industries
- Actively support MSD energy reduction programs across the division and share best practices with other sites.
- Participate in the MSD Ireland and European Energy Forum

Qualifications

Ideally interested candidates should have the following qualifications & Experience:

- Honours degree in Engineering or equivalent discipline
- Minimum of 5 years experience
- Formal training or qualification in energy management would be preferred
- Leadership & coaching skills to further build an energy management culture on site & maintain sponsorship for energy programs.
- Excellent analytical and problem solving skills, coupled with the ability to generate innovative technical solutions as required
- LSS skills – ideally Green Belt or above.
- Experience in an equivalent energy management or Utilities engineering/management role
- Good commercial awareness – having delivered value adding or money saving projects.
- Good understanding of utility equipment, building services, building automation systems and HVAC
- Experience in a Pharma or regulated environment would be preferred
- Strong interpersonal, communication & project/portfolio management skills
- Excellent verbal and written communication skills
- Strong financial skills

*LI-SC1

Job: Engineering Generic

Job Title: Site Energy Lead

Primary Location: EMEA-Ireland

Employee Status: Regular

Number of Openings: 1

External Job Board Posting: Ireland - IrishJobs.ie

Director, Public Policy French Africa Job (Casablanca, MA)

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Director, Public Policy French Africa-GLO000281

Description

PUBLIC POLICY

- In close consultation with Country and Business Directors, develop and manage the implementation of national advocacy strategies that support MSD policy goals, and position MSD as a leading innovative and responsible research?based pharmaceutical company committed to improving the health of society.
- Actively collaborate with communications, market access and business teams to bring the field perspective to MSD’s public policy and communications efforts, including the development of public policy, advocacy and media messages and web content.
- Participate in the planning and implementation of events, conferences, and other special events relating to policy
- Ensure that healthcare systems embrace policies that recognize & reward innovative medicines
- Reduce trade barriers & protectionism affecting the entry & marketing of innovative products
- Advance the policy agenda for public sector vaccine programs for innovative products
- Ensure as MSD, and through industry leadership, that Government policy supports the innovative pharmaceutical sector in a way that enhances the success of innovative products
- In coordination with regional partners seek opportunities to make a difference in people's lives and advance human health through the deployment of corporate philanthropy and corporate responsibility in a way that enhances our reputation
- Work with MSD country management to build up local Public Policy capacity to support achievement of the business plan and other strategic goals

INTERNAL PARTNERSHIPS

- On a daily basis: Managing Directors, Executive Director External Affairs / Policy, Business Operations, Commercial, Marketing, Regulatory, Medical Affairs, Legal and Market Access Leads.
- On a frequent basis: Policy colleagues in Brussels and Washington DC offices

Qualifications

- The ideal candidate would have extensive industry experience in policy/government/corporate affairs or medicine/pharmacology, business administration, legal, political science and communications background as a foundation
- In terms of job experience, suitable candidates may be found with legal, communications, regulatory, market access, marketing or general management background
- Fluency in English and French is required, Arabic is preferred
- Confident and articulate communication both in writing and in person
- The ability to work well in teams and cross functionally with stakeholders outside the Company, including government officials, industry competitors, diplomats and the media
- Strong problem-solving and analytic skills
- Strong diplomatic skills, energy and creativity that can drive an ambitious policy agenda

Job: Global Policy/Communications

Job Title: Director

Primary Location: EMEA-Morocco-Grand Casablanca-Casablanca

Other Locations: EMEA-CH-LU-Luzern

Employee Status: Regular

Travel: Yes, 50 % of the Time

Number of Openings: 1

Senior Specialist Compliance & Risk Management Job (EMEA-Netherlands)

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Senior Specialist Compliance & Risk Management-COM000183

Description

For our MMD IT Compliance department we are currently looking for a:

Senior Specialist Compliance & Risk Management

About MSD

MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies, consumer care and animal health products, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD has a workforce of over 6.000 in the Netherlands at five different sites. For more information, visit our website www.msd.nl or www.msd-animal-health.nl/

Organization

The MMD IT Compliance department is a global, above-site team of subject matter experts (SMEs) on the field of IT Compliance and risk management within the MMD and Animal Health (AH) divisions. The main objectives of this team are:

- Identifying, communicating and mitigating risk in the area of regulatory (GxP, SOX, Data Privacy, etc) IT and automation compliance;

- enabling a continuous, cost-effective and business efficient IT compliance by application of Quality by Design (QbD), sigma and continuous improvement principles.

The position

The Senior Specialist IT Compliance & Risk Management is responsible for providing overall IT/ automation compliance and inspection leadership to the IT site teams across a number of our MMD and AH facilities in mainland Europe. In addition to the site based IT teams, this function will also support the global (above site) animal health IT teams, based in Boxmeer (The Netherlands). As part of this the Senior Specialist IT Compliance & Risk Management will be responsible for:

- Monitoring and managing IT compliance risks in the assigned sites and (sub)regions; .

- Acting as a credible change agent to assure consistency in direction, practice, focus and alignment of global, regional and site IT and related computer system validation compliance;
- Developing, training and/ or enforcing system development lifecycle (SDLC) standards and supporting tools ( job aids, best practices, etc) in alignment with corporate and divisional policies, guidelines all applicable legal and regulatory requirements (e.g. EU Eudralex Vol 4, Annex 11; 21 CFR Part 210/211/11, SOX 404, etc) and industry standards (e.g. Good Automation Manufacturing Practices (GAMP));

- Developing, training and/ or enforcing compliance with IT security and identifying/ accessing management requirements, policies, standards and tools, to ensure security and effective management of Merck information and technology;

- Providing hands-on CSV/ IT compliance guidance for strategic projects.

- Full management of IT compliance related projects, including budgets and (external) resources;

- Aligning with various IT, business and quality functions on IT Compliance practices, positions and issues;

- Periodically supporting IT assessment and auditing of MSD/Merck & Co. internal sites as well as suppliers.

- Accountable for the successful realisation of all IT and Automation related projects across the sub-region;

- Acting as the focal point for interactions and escalations back to all IT shared-service functions;

- Contributing to the development and driving the local execution of the global IT strategy;

- Managing IT demand, IT portfolio planning, forecasts and updates across the sub-region.

The role will report into the MMD-IT Director, Compliance & Risk Management for Continental Europe, Africa, AP/J & Animal Health.

The role can be either based in The Netherlands or Belgium and he/ she will be travelling up to 25% of the time within the Continental Europe area.

Qualifications

The candidate

- Minimum Bachelor's Degree - BS in Engineering, Chemistry, Computer Science, or other technical degree;
- At least 10 years of working experience in a Health Authority regulated environment (Pharmaceuticals, devices, etc);

- At least 5 years of working experience in a pharmaceutical IT compliance, Computer System Validation or related field;

- Strong knowledge of GxP laws, rules and regulations (Examples: Eudralex Volume 4, 21CFRPart 210/211/11) and related industry guidance on (e.g. GAMP 5 and related Good Practice Guides);

- Experience in both execution and coordination of validation projects for GxP applications;

- Strong knowledge and experience in the field of risk management (including FMEA);

- Ability to identify, analyse & articulate potential compliance challenges as well as ability to make recommendation on addressing those challenges;

- Result driven team player with the ability to work independently, set priorities and collaborate with peers and management to remediate identified risks and potential compliance issues;

- Strong communication and collaboration skills, being diplomatic and able to compromise;

- Analytical thinking, problem solving capabilities and strong attention to detail;

- Ongoing focus on identification and realization of improvement potential;

- Affinity for IT and automation systems;

- Excellent oral and written skills in English (Dutch and/ or other languages are a plus).

- Experience in working with regional, cross-cultural and cross-divisional teams (a plus);

- Experience in SOX and data privacy (a plus);

- Experience in Six Sigma or equivalent process optimisation principles (a plus).

A good place to work

MSD is an attractive employer offering interesting opportunities in Research & Development, production and staff departments for an enormous range of disciplines such as biologists, chemists, process engineers, technicians, mechatronic engineers, pharmacists and operators. MSD always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD values and rewards most. If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Information
For further information regarding this position, you can contact Tim Goossens, MMD-IT Director, Compliance & Risk Management for Continental Europe, Africa, AP/J & Animal Health,

+32 496.86.42.32.

Application

If you are interested in this position, you are invited to apply online.

*LI-RS1

Job: Compliance & Risk Management

Job Title: Senior Specialist Compliance & Risk Management

Primary Location: EMEA-Netherlands

Employee Status: Regular

Travel: Yes, 25 % of the Time

Number of Openings: 1

Manager Global CMC Regulatory Affairs - Supply Job (EMEA-Netherlands)

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Manager Global CMC Regulatory Affairs - Supply-REG001119

Description

For our location in Oss (The Netherlands) we are currently recruiting a:

Manager Global CMC Regulatory Affairs - Supply

About MSD

MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies, consumer care and animal health products, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD has a workforce of over 6.000 in the Netherlands at five different sites. For more information, visit our website www.msd.nl or www.msd-animal-health.nl/

The position

MSD has a challenging opening for a candidate who not only can demonstrate CMC regulatory expertise, but also management capability. The successful candidate will lead a team located in Oss (The Netherlands) that currently encompasses 8 staff members and 2 contractors responsible for the maintenance of existing chemical and pharmaceutical manufacturing and controls (CMC) worldwide registrations. This is done through:

·

* Supervising/ coordinating/ preparing/reviewing the chemistry, manufacturing, and controls information for worldwide marketing of pharmaceutical products (NDA, WMA, MAA) to include annual reports, registration renewals, supplements, variations and responses;

* · Defining the strategy for filing post approval changes, responding to agency or subsidiary questions;

* · Prioritizing workload for the team;

* · Resolving issues;

* · Corresponding continuously and interacting with regulatory agencies and other Merck scientists to support in-line product filings worldwide;

* · Maintaining a working knowledge of current governmental and worldwide requirements for re-registration and post-approval changes;

* · Assuring that that filed information on the current manufacturing and testing procedures is kept updated for each product using appropriate departmental systems;

* · Ensuring consistency in practices, championing best practices and promoting operational excellence;

* · Partnering with others in the pharmaceutical industry and regulators to reduce the regulatory burden of making post approval improvements in CMC;

* · Identifying initiatives to promote Operational Excellence;

* · Supporting new and existing CMC systems (RCAM, ORION, QSIS) and assuring compliance with those systems;

* · Supporting staffing needs, training, promoting growth through new opportunities and understanding of each person's Employee Development Plan;

* · Identifying and promoting best practices within CMC;

* · Maintaining superior knowledge of current government regulations and worldwide requirements for initial registration, re-registration and post-approval changes;

* · Demonstrating leadership in departmental improvement activities such as system modifications, maintenance of standard operating procedures, internal guidelines, etcetera;

* · Participating in external discussion groups, societies, working groups to influence market requirements, promoting harmonization, and reducing the regulatory burden;

* · Identifying internal and external customer needs and leading the team in accordance with those needs.

Qualifications

The candidate

* · Degree in pharmacy, bio-pharmaceutics, analytical chemistry, organic chemistry, chemical engineering or a related discipline;

* · At least ten years of industrial experience in chemical/ pharmaceutical research or manufacturing including processing and/ or analytical testing;

* · Working knowledge in quality assurance and quality systems (a plus);

* · Significant knowledge of regulations related to CMC;

* · Able to manage projects to achieve high productivity, prioritizing, and managing effective meetings;

* · Effective leadership;

* · Providing strategic direction and facilitating changes needed to move in that direction;

* · Innovative, flexible and collaborative;

* · Demonstrated problem solving and decision making skills;

* · Positive vision for the future of Merck/ MSD;

* · Awareness of Merck’s/ MSD’s overall business objectives and strategies;

* · Working knowledge of Word, Excel, PowerPoint and Document Management Systems;

* · Superior oral and written communication skills in English, Dutch and/or other languages are preferred.

A good place to work

MSD is an attractive employer offering interesting opportunities in Research & Development, production and staff departments for an enormous range of disciplines such as biologists, chemists, process engineers, technicians, mechatronic engineers, pharmacists and operators. MSD always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD values and rewards most. If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Information

For more information about the vacancy, please contact Tom Sam, Head Global CMC Regulatory Affairs, by phone: +31 6 101 837 60 or via e-mail tom.sam@merck.com.

Application

If you are interested in this position, you are invited to apply online.

Job: Regulatory Affairs - CMC

Job Title: Manager Global CMC Regulatory Affairs - Supply

Primary Location: EMEA-Netherlands

Employee Status: Regular

Number of Openings: 1

Vendor Manager Job (Oss, NL)

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Vendor Manager-PRO010461

Description

For our Global Clinical Supply (GCS) department in Oss (The Netherlands) we are recruiting a:

Vendor Manager

About MSD

MSD is working to help the world be well. Through our medicines, vaccines, biologic therapies, consumer care and animal health products, we work in more than 140 countries to deliver innovative health solutions to patients and animals. We also demonstrate our commitment to increasing access to health care through far-reaching programs that donate and deliver our products to the people who need them. MSD has a workforce of over 6.000 in the Netherlands at five different sites. For more information, visit our website www.msd.nl or www.msd-animal-health.nl/

The department

Global Clinical Supply (GCS) is responsible for ensuring the timely supply of Investigational Medicinal Products to support Merck/MSDs global clinical development portfolio. The department supports hundreds of clinical studies in phases I to IV, across the globe. Working closely with Clinical and Supply Chain colleagues, we ensure a well-designed, high quality product reaches the patient at the right time, every time.

The position

The Vendor Manager is responsible for coordinating the day to day activities related to sourcing of clinical supply chain services, such as packaging and labeling at approved suppliers. He/ she works independently with general direction from the Vendor Management Lead EU. Assigned projects will require utilization of team resources and may include working cross-functionally. This position requires project management of the multiple related activities for the set-up of packaging execution of a clinical protocol/ program at a vendor, providing key support to the associated clinical supplies functions. As part of this the Vendor Manager will be responsible for:

· Setting up cost estimates and budgets for planned work on a protocol basis. Assisting Vendor Management Lead in forecasting on an annual and ad hoc basis;

· Initiating Purchase Orders for outsourced projects when applicable;

· Ensuring individual protocol cost estimate is maintained and managed/updated when appropriate;

· Providing technical expertise to internal project team, working cross functionally with GCS Planning, Quality and Clinical where appropriate; delineate vendor capabilities and provide creative/ key technical consultation into clinical supply strategy as required;

· Coordinating submission of RFQ (request for quote);

· Receiving and reviewing vendor quotation, providing technical feedback and driving vendor selection;

· Ensuring adherence to market value or agreed pricing arrangements for all services requested;

· Attending (and managing where appropriate) vendor business review meetings, site visits and technical update meetings;

· Ensuring adherence to project budgeting;

· Receiving and independently reviewing outsourcing request from internal personnel;

· Managing clinical supply delivery timeline of clinical programs and/or multiple complex projects ranging from Phase I though IV in conjunction with chosen vendor to ensure customer expectations are met;

· Working cross functionally, coordinating the necessary internal resources to ensure vendor timelines can be achieved and flag issues for resolution;

· Resolving project issues from a technical and timing perspective and provide PM oversight (e.g. hold project review meetings as appropriate) to ensure timely availability of clinical supplies to meet Clinical Development program requirements;

· Providing training/ mentoring to new/ existing personnel on technical activities concerning clinical supplies including outsourcing methodology;

· Participating, as appropriate, in third party process re-engineering and process improvement initiatives to enhance efficiency and alignment with external and internal partners.

This position also requires the development of interface procedures between suppliers and Merck to effectively facilitate the sourcing process, in addition to identifying productivity improvements to these interfaces. Additionally, for high stakes suppliers, this position may provide direct operational oversight of the supplier. This position is predominantly charged with driving cost effective, technically sound packaging, labeling and distribution activities.

Qualifications

The candidate

- Degree in pharmacy, bio-pharmaceutics or a related discipline;

- At least five years of industrial experience in chemical/ pharmaceutical research or manufacturing;

- Strong technical knowledge of clinical packaging/ labeling and distribution, supplemented with knowledge from clinical manufacturing;

- Strong project management skills to ensure a quality and timely product is delivered to the patient;

- Ability to establish strong strategic relationships outside of Merck;

- Ability to effectively coordinate, integrate, communicate, monitor/ measure, report and streamline the process by which investigational products are progressed from formulation to tangible clinical supplies;

- Innovative, flexible and collaborative;

- Demonstrated problem solving and decision making skills;

- Working knowledge of Word, Excel, PowerPoint and Document Management Systems;

- Superior oral and written communication skills in English, other languages are preferred.

A good place to work

MSD is an attractive employer offering interesting opportunities in Research & Development, production and staff departments for an enormous range of disciplines such as biologists, chemists, process engineers, technicians, mechatronic engineers, pharmacists and operators. MSD always seeks ‘best-in-class’ employees at all levels. We expect a lot from our people and MSD has a lot to offer them as well. Team spirit, entrepreneurship, integrity, leadership and cross-border communication skills are what MSD values and rewards most. If you enjoy being challenged, over and over again, MSD will be a good place for you to work. We have an excellent fringe benefit program, and we invest heavily in the development of our people. MSD gives you plenty of opportunities for individual initiative and responsibility.

Information

For more information about the vacancy, please contact Justin Chapman, Associate Director, Global Clinical Supply, by phone: +44 1992452246 or justin.chapman@merck.com

Application

If you are interested in this position, you are invited to apply online.

*LI-RS1

Job: Product Dev Proj/Prog Mgmnt

Job Title: Vendor Manager

Primary Location: EMEA-NL-NB-Oss

Employee Status: Regular

Number of Openings: 1

Manager - Medical Affairs (Speciality II - Kolkata) Job (Kolkata, IN)

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Manager - Medical Affairs (Speciality II - Kolkata)-SAL003318

Description

Primary scientific face of MSD for SLs/OLs

• Spearhead implementation of research activities: directed towards enhancing research capabilities, generation of clinical/epidemiological evidences, Merck Investigator Studies Program (MISP) etc

• Spearhead implementation of educational activities: directed towards dissemination of evidence based clinical guidelines and best practices, establishing local academic networks, enhancing translation of guidelines in to practice and improving overall treatment patterns

Primary scientific resource for the sales team

• Training on therapy area, disease and products at induction and on ongoing basis

• Responding to all relevant scientific clinical queries raised by HCPs

• Speaker briefing and conduct of scientific meetings planned by sales & marketing team

• Scientific, non-promotional resource for implementation of other marketing campaigns of marketed products

• Reporting of adverse events related to MSD products

• Compliance advisor for sales and marketing activities and for promotional practices

Conflict of interest management

• To ensure scientific sanctity of all promotional and non-promotional activities being conducted by or on behalf of MSD

• To carefully avoid any inadvertent linkage of educational or research activities with commercial returns

Self development

• To update self on scientific developments in the respective therapy areas, not only to ensure professional development but also to ensure proper execution of responsibilities mentioned above

• To work on special project(s) of the department, including those related pipeline products, allocated primarily with the objective of job enrichment and career growth

• To acquire skills and strengths required to realize carrier development plans

Qualifications

• Medical Graduate having a MCI recognized degree

• Candidates with post graduate degree/diploma would be given preference

Job: Sales

Job Title: Specialist - Medical Affairs

Primary Location: APAC-IN-WB-Kolkata

Employee Status: Regular

Travel: Yes, 75 % of the Time

Number of Openings: 1
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