Process Engineer Viral Vectors | Biologe (m/w/d)
ProBioGen AG
Job Summary
This role is ideal for a Biologist or Process Engineer specializing in viral vectors within the biopharmaceutical industry. The professional will be based in Berlin, focusing on the GMP production of sterile, viral drug products for clinical trials. Day-to-day responsibilities include executing and monitoring aseptic filling processes and visual inspections according to EU GMP Annex 1, planning vial integrity testing, and operating state-of-the-art process equipment. A critical component of the job involves maintaining GMP compliance through the creation and updating of SOPs and material specifications, as well as continuously optimizing existing processes for efficiency. The position requires close collaboration with interdisciplinary teams to support the transfer of processes from development into full production, offering the chance to be an innovation driver in new therapeutic developments, particularly in areas like cancer treatment.
Required Skills
Education
Completed natural science degree in Biotechnology, Bioprocess Engineering, Biochemistry, or comparable qualification
Experience
- Professional experience in the (bio)pharmaceutical environment is advantageous
- Professional experience in a GMP production environment, ideally in sterile filling, is advantageous
- Experience working with viruses or viral vectors is desirable
Languages
Additional
- Willingness to work with organisms of genetic engineering safety level 2 (viruses) and perform visual inspections of the filled product.
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