Assist with technology transfer & manufacturing of Verve's novel gene editing products to drive successful clinical supply by external vendors.
Minimum Requirements:
- Bachelor's Degree (foreign equivalent acceptable) in Biomedical or Chemical Engineering, Pharmaceutical Development or related field
- 5 years post-degree biotech or biopharmaceutical experience in LNP & API manufacturing
Experience must include any amount of the following:
(1) Following common practices & using equipment to run & troubleshoot manufacturing processes in GMP environment including vacuum dryers, solvent extraction & partitioning, mixers, filtration, & sterile/aseptic process
(2) Implementing FAT & SAT of GMP/Non-GMP equipment
(3) Authoring regulatory documents for commercial & clinical products
(4) Knowledge of GMP compliance around drug product & API manufacturing, demonstrated by prior experience operating in GMP-regulated environment through technology transfer & manufacturing practices
Alternative Qualification:
Master's Degree (foreign equivalent acceptable) in Engineering, Pharmaceutical Development, or related field with 2 years biotech or biopharmaceutical experience in LNP & API manufacturing, including experience with items 1-4 listed above.
Additional Details:
- Up to 25% domestic & international travel
- Work from home allowed 2 days per week
Application Instructions:
Email resumes to Careers@Vervetx.com with reference to Job Code: VTCK25. No phone calls.
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