Manufacturing Technical Writer (6+ Month Contract)

Rentschler Biopharma SE; Milford (MA); On-site; USD 52,000 - 69,000; Full time

Job summary

Rentschler Biopharma SE in Milford, MA, seeks a Manufacturing Technical Writer to generate, revise and manage GMP documentation for upstream production, including batch records, SOPs and work instructions.

You will own document workflows and collaborate with Manufacturing Operations, MSAT, Process Engineering, Quality and Training to ensure documentation is completed on schedule and training is aligned in a fast-paced biopharma environment.

Qualifications

• Bachelor's degree in Life Sciences or related field required.
• Experience authoring GMP and technical documents for new and existing processes.
• Ability to collaborate across Manufacturing Operations, Quality, and Training teams.

Responsibilities

• Create, revise, and manage Upstream Master Production Records (MPRs) and GMP documents.
• Develop and maintain manufacturing instructions for upstream cell culture operations and single-use bioreactor systems.
• Own document workflows in quality systems with routing, approval, revision control, and training alignment.
• Partner with Manufacturing Operations, MSAT, Process Engineering, Quality, and Training to ensure on-time completion.

Skills

Bachelor's degree

GMP documentation experience

Cross-functional collaboration

Documentation management

Education

Bachelor's degree in Life Sciences / Biopharma

Tools

MasterControl

TrackWise

Job description

locationsMilford, MA, United Statestime typeVollzeitposted onVor 3 Tagen ausgeschriebenjob requisition idJR2816Advancing 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.The Manufacturing Technical Writer will be responsible for creating, revising, editing GMP documentation such as manufacturing batch records, SOPs and work instructions.Duties and ResponsibilitiesGenerate, 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.QualificationsBachelor’s Degrees is requiredBiopharmaceutical 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 documentsExperienced with user role in quality documentation systems such as Master control and/or Track wiseSelf-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 deadlinesWorking ConditionsLab environmentOffice environmentPhysical RequirementsPPE as required____________________________________________________________________________Base Pay Range$38/hr - $50/hrDisclosure StatementRentschler Biopharma, Inc is committed to fair and equitable compensation practices. The base pay range listed for this position is the anticipated annual base salary range the organization reasonably, and in good faith, expects to pay for this position at this time. Actual compensation is determined based on several factors that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other application factors permissible by law. The annual base salary is just one component of our Total Rewards package, which also includes our annual discretionary bonus program, medical insurance, our generous 401K program, plus a host of other benefits to aligned to support our employees’ personal and professional wellness. The salary pay range is subject to change and may be modified at any time.Brauchen Sie Hilfe?Wenn Sie Unterstützung beim Hochladen Ihrer Bewerbung brauchen, wenden Sie sich bitte an unser Recruiting-Team: [e-mail]