Specialist, Manufacturing
$74,000–$118,400 year
On-site · Norwood, Massachusetts, United States
Job Summary
Specialist, Manufacturing drives cGMP-compliant drug product operations, owning defined manufacturing focus areas, leading investigations and CAPAs, supporting tech transfer and qualification/validation activities, and mentoring others. KEY responsibilities include on-floor support across start-up, routine production, and troubleshooting; developing and managing GMP documentation; driving Lean/Six Sigma improvements; managing scheduling across projects; delivering training to staff; and ensuring adherence to regulatory standards. The role requires a Bachelor's degree in Engineering, Life Sciences, or related field, 5-8 years of biopharmaceutical manufacturing experience (advanced degree preferred), and US work authorization with no visa sponsorship. The position is site-based at Moderna and not eligible for remote work, located in Norwood, MA, USA, with a salary range of $74,000 to $118,400 per year. Beneficial skills include Lean Six Sigma, SAP/MES, electronic batch records, and experience with fill/finish, aseptic operations, and regulatory readiness.
Required Qualifications
- Bachelor’s degree in Engineering, Life Sciences, or a related field
- 5-8 years of experience in biopharmaceutical manufacturing operations
- Experience with deviation/investigation management systems and technical writing in a cGMP environment
- Experience with buffer prep, formulation, aseptic manufacturing operations, isolator technology, media fills, automated visual inspection, automated labeling & packaging, or serialization preferred
- Site-based role; US work authorization required; no immigration sponsorship available
Additional Requirements
- Must have US work authorization; Moderna cannot sponsor visas
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.