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Process Engineer, External Manufacturing / MSAT (Cell Therapy / Viral Vectors)
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- On April 3, 2024, we announced closure of a significantly oversubscribed $160.5 million Series C financing with a top-tier syndicate of life science investors led by new investor, Wellington Management.
- The ideal candidate will have experience overseeing work completed at a CDMO/CMO and a strong background in cGMP requirements and their application to viral vector and mammalian cell culture manufacturing.
- Collaborate with cross-functional teams, including the CDMO joint project team, Obsidian Process and Analytical Development, Quality Assurance, Quality Control, and Regulatory to assure effective tech transfers and start-up of new manufacturing processes according to agreed upon timelines in support of business objectives.
- Bachelor's degree in biological sciences, (bio)chemical engineering, or related discipline with 5+ years of experience (or MS with 3+ years) working in a Manufacturing or MSAT role in the Cell Therapy and/or Viral Vector space.
- Strong understanding of aseptic processing and cGMP requirements and their application to viral vector and mammalian cell culture manufacturing.
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