Manufacturing Technical Writer (6+ Month Contract)

Rentschler Biopharma • Milford, MA

4d • Hybrid

About The Position

Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases. Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions – together with our clients. Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability. As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.

Requirements

• Bachelor’s Degrees is required
• Biopharmaceutical manufacturing processing in a GMP compliance environment (e.g. Production, Development, Process Engineering, Technical Services or related field)
• 5+ years’ experience in manufacturing, quality & compliance (Clinical, Commercial, Medical Device, MedTech)
• Author of GMP and technical documentation for new and existing processes; Process technical documents, Manufacturing description documents, SOPs, Batch records, Solution records and Training documents
• Experienced with user role in quality documentation systems such as Master control and/or Track wise
• Self-initiator, strong collaborator, proven dot connector, results driven, ability to clearly track work status and communicate to relevant departments, strong capability to resolve challenges to meet deadlines

Responsibilities

• Generate, revise, and manage Upstream Master Production Records (MPRs) and associated GMP documentation, including batch records, SOPs, and work instructions, ensuring accuracy, compliance, and on-time implementation.
• Serve as the documentation lead for upstream manufacturing processes, utilizing knowledge of cell culture operations, subcultivation, perfusion, and single-use bioreactor systems to develop and maintain manufacturing instructions.
• Own document workflows within quality systems, including document creation, routing, review, approval, revision control, and implementation activities.
• Partner with Manufacturing Operations, MSAT, Process Engineering, Quality, and Training teams to ensure documentation is completed on schedule, assigned to the appropriate departments, and supported by the appropriate training strategy.

Benefits

• annual discretionary bonus program
• medical insurance
• generous 401K program
• other benefits to aligned to support our employees’ personal and professional wellness

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level