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Associate Scientist Stability Novel Vaccines | Big Pharma | Leiden

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The company

Our client is a professional Pharmaceutical and Biotechnology organisation, based in Zuid-Holland Netherlands. Janssen Vaccines & Prevention, one of the Janssen Pharmaceutical Companies of Johnson & Johnson, is dedicated to bringing meaningful innovation to global health. Our teams focus on the discovery, development, manufacture and marketing of vaccines and antibodies to protect people worldwide from infectious diseases. In our organization entrepreneurial people work in a dynamic culture in which innovation and a 'can do' state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to Janssen.

Role description

Product stability team is part of the Analytical Development Department of Janssen and focuses on the design, execution and evaluation of stability profiles of novel vaccines. The group supports the clinical development stages of the vaccines platforms and generates data that is used in preparation for future commercialization.

Responsibilities

The Associate Scientist will be a key player in the support of the various stability studies of the novel vaccines during the clinical development. You will work in a multidisciplinary environment and have a focus on preparation of various documents such as stability protocols, stability reports, amendments, shelf-life extensions. The person will support other Stability scientist in daily management of studies by preparation of data tables, evaluation and visualization of data trends and communication to relevant stakeholders.

Since different CMC projects are carried out in teams comprising members from different departments, teamwork and flexibility are two very important characteristics that are required attributes. We offer a challenging position which allows you to work in a dynamic and international environment, ensuring diversity in your work and creating plenty of opportunities for personal development.

Requirements

• BS or MS Degree in Biochemistry, Pharmacy, or equivalent life sciences degree
• A minimum of 2-3 years pharmaceutical industry experience working under GMP standards.
• Preferably experience with stability studies (design, reporting, ICH requirements)
• Understanding of analytical methods qualification and validation
• Knowledge of data trending

Other information

This is a fixed-term assignment for a maternity leave cover.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Cees Roffelsen.

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SIRE Life Sciences®

Listed by: SIRE Life Sciences®
Listed on: 12-02-2019
Country: The Netherlands
Region: Zuid-Holland
Employment: Permanent
Expertise: 3 - 5 years
Location Type: On location
Education: Bachelor
Language: English
Sector: Pharmaceutical
Specialisation: Research & Development

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