MSAT Project Lead - Biologics Tech Transfer

Recordati; Bridgewater (MA); Hybrid; USD 121,000 - 181,000; Full time

Benefits offered by this job

Medical, dental, vision coverage

401(k) retirement savings plan

Life and AD&D insurance

Short/long-term disability

Paid time off and holidays

Job summary

Recordati Rare Diseases, Inc. (RRD) seeks an experienced MSAT professional to lead technology transfer of commercial biologics to CDMOs and partners, while supporting lifecycle management across multiple therapeutic areas.

The role spans cross-functional collaboration with global teams and may involve travel for partner coordination. The ideal candidate will have a life sciences degree, 5+ years in pharma/biologics, and strong knowledge of CMC, quality systems, and regulatory interfaces.

Qualifications

• Minimum degree in a science-related field, preferably life sciences.
• Five years of industry experience in a pharmaceutical/manufacturing setting with exposure to biologics.
• Experience working virtually/remotely is desirable.

Responsibilities

• Lead technology transfer projects for long-term biologics manufacturing at CDMOs and partners.
• Generate and review technical documentation (master plans, process descriptions, gap assessments) for transfer.
• Support lifecycle management of Recordati's biologics across development stages.
• Collaborate with global teams and external partners; travel as required (approx. 30%).

Skills

CMC knowledge

Biologics manufacturing

Process development

Regulatory/CMC

Analytical methods

Quality systems

Education

Science degree

Job description

Recordati Rare Diseases, Inc. (RRD) seeks an experienced MSAT professional to lead technology transfer of commercial biologics to CDMOs and partners, while supporting lifecycle management across multiple therapeutic areas.

The role spans cross-functional collaboration with global teams and may involve travel for partner coordination. The ideal candidate will have a life sciences degree, 5+ years in pharma/biologics, and strong knowledge of CMC, quality systems, and regulatory interfaces.