Are you enthusiastic about writing and do you have experience with quality management systems? This can be the right job for you! As a Scientist, you will be responsible for the extraneous agents safety of products developed by Janssen Vaccines Leiden. Furthermore, you will monitor extraneous ...
CLS Services is a leading professional recruitment agency, specialised in the recruitment and career coaching of people with a background in chemistry & life sciences. For our client, Janssen Vaccines & Prevention, we are searching for a Scientist Analytical Development.
Janssen Vaccines & Prevention is dedicated to bringing meaningful innovation to global health. They focus on the discovery, development, manufacturing and marketing of vaccines and antibodies to protect people world-wide from infectious diseases.
The Analytical Development department within Janssen Vaccines Leiden (one of the pharmaceutical companies of Johnson & Johnson) is responsible for developing methods that are required for analysis of vaccines for human use. Analysis includes testing for identity, quantity, potency, purity and contamination; in particular, extraneous agents safety.
Are you enthusiastic about writing and do you have experience with quality management systems? This can be the right job for you!
As a Scientist, you will be responsible for the extraneous agents safety of products developed by Janssen Vaccines Leiden. Furthermore, you will monitor extraneous agents safety method performance and ensure method development of in-process control and release methods to be conducted at GMP level in-house and at contract laboratories. Demonstrating flawless documentation, effective communication with varied levels of the organisation, a strong sense of responsibility and a passion for quality are key competencies for this position.
Who we're looking for
We are looking for a highly motivated Scientist with a PhD in a relevant discipline and who enjoys working in a multidisciplinary team. You have experience with:
- Microbiology (e.g., prions/TSE, viruses, microbials) and/or cell biology;
- Assay development and validation of cell-culture based and/or molecular methods (e.g., mammalian cell culture, TCID50, PCR, sequencing);
- Biopharmaceutical manufacturing (preferred);
- Excellent writing skills.
The ideal candidate has at least 2 – 5 years of experience in method development and at least one year experience with cGxP or other quality management systems. Next to that, you are fluent in English.
Additional vacancy information
Contract: Temporary contract with CLS Services
Terms: Project for at least 1 year, longer-term possibilities anticipated. Full time highly preferred, 36 hours discussable.
Contactperson: Claudia Erwich-Faaij
Phone: +31 (0)88 22 77 555
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