Gmp Manufacturing Operations Support
Responsible for supporting GMP manufacturing operations through high-quality technical documentation, deviation investigation ownership, and cross-functional operational support for clinical and/or commercial drug product manufacturing. This role is responsible for authoring, reviewing, and managing deviations, CAPAs, technical reports, SOPs, batch record updates, and manufacturing documentation to ensure compliance with cGMP regulations, ALC
Sr. Specialist Deviations & Technical Writing, Drug Product
Randstad · Norwood, MA, USA ·
- Job type:
- Full Time