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Associate Scientist | 6 months

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The company

Our client is a professional Pharmaceutical organisation, based in Zuid-Holland Netherlands. This company is committed to developing first-in-class or best-in-class vaccines for some of the world's most life-threatening infectious diseases. They have built a dedicated, world-class, multi-functional team across a variety of disciplines to develop a promising vaccines pipeline. In Leiden they have a workforce of 700 scientists and support staff, 45% of their employees have a nationality other than Dutch with over 20 nationalities represented. They partner with many of the world's leading experts, academic and clinical institutions and other pharmaceutical companies for the development of vaccines against, for example: Ebola and HIV.

Role description

The drug-substance development (DSD) department is responsible for the development of scalable, pharmaceutical-grade USP and DSP processes for viral vaccines using mammalian cell lines as a production platform. Novel technologies are used to make sure that the processes are safe, reliable, scalable and cost-effective. So that the vaccines can be produced in large quantities at low costs. The developed processes are transferred into GMP production facilities for the production of clinical batches and scaled-up for commercial production. All activities are performed in close collaboration with other departments.

Responsibilities

- Natural organisational talent to coordinate logistics of sample distribution, including their required data to other departments
- Keeping oversight of required documentation and needs at all times
- Ensure completion of dossiers by chasing/keeping track of missing data records, data validation
- Keeping all parties aligned at all times

Requirements

- MSc, PdEng or PhD in a relevant discipline in biopharmaceutical / biomedical sciences/engineering, biotechnology
- Some experience in process development (lab/production/biotechnology)
- Experience with production, technology transfer, batch records, data validation and knowledge of GMP is an advantage.
- English required, Dutch is a plus
- Eye for detail / accurate
- Stress resilient
- Strong in communication
- Proactive/can work without too much guidance

Other information

Full time preferred

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


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SIRE Life Sciences®

Ref. number: 47955
Listed by: SIRE Life Sciences®
Listed on: 13-06-2019
Country: The Netherlands
Region: Zuid-Holland
Employment: Freelance
Expertise: 0 - 2 years
Location Type: On location
Education: Master
Language: English
Sector: Pharmaceutical
Specialisation: Pharmacology

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