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Open nowPosted 20 days ago

Technical Author

Bachem SA

Where
Vionnaz, VS, Switzerland
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Your applicationOpen nowTechnical AuthorBachem SA · Vionnaz, VS, Switzerland

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Share of postings closed within
  1. 2.0%1 day
  2. 4.3%3 days
  3. 11.5%7 days
  4. 18.1%14 days
  5. 35.6%30 days
  6. 44.6%60 days
This job: posted 20 days ago

The posting

Bachem is a world leader in the development and manufacture of peptides and oligonucleotides for thepharmaceutical industry. To strengthen our Technical Operations team in Vionnaz (Valais, Switzerland), we arelooking for a Technical Author (all) 100% . As a key member of TechOps, you will create and maintain GMP manufacturing documentation, supporttechnology transfer and new product introduction projects, and ensure process knowledge is translated intocompliant, manufacturing-ready records. You will also contribute to the implementation of eMBPR and thedigitalization of manufacturing documentation. Your key responsibilities Create, review, and maintain GMP documentation supporting manufacturing operations and technologytransfer activities. Prepare Master Batch Production Records (MBPRs), manufacturing instructions, protocols, reports, andrelated technical documents. Translate process knowledge and development data into compliant, manufacturing-ready documentation. Collaborate closely with Process Scientists, laboratory teams, Manufacturing, and Quality Assurance. Support technology transfer projects from process familiarization through commercial implementation. Participate in new product introduction projects and manufacturing readiness activities. Ensure documentation complies with GMP requirements, internal procedures, and regulatoryexpectations. Contribute to the implementation of eMBPR and the standardization and digitalization of manufacturingdocumentation. Your Profile Master's degree or PhD in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or arelated discipline. Strong scientific background with a solid understanding of chemical and pharmaceutical manufacturingprocesses. Minimum 3 to 5 years of experience in a GMP-regulated pharmaceutical or chemical environment. Experience in technical writing, manufacturing documentation, technology transfer, or processdevelopment. Familiarity with batch record creation and document management systems. Excellent technical writing skills with strong attention to detail and a structured approach. Fluent in French and English (minimum C1 level). German is a strong asset. Proactive team player with strong organizational and communication skills; Our offer A modern and dynamic working environment within a fast-growing international company. Challenging projects of high scientific and technical value. Opportunities for professional development and continuing professional development. A corporate culture based on collaboration, innovation and excellence. Attractive working conditions and competitive employee benefits. Interested? Would you like to drive innovation together with us? We look forward to receiving your complete application documents via our application portal. Learn more about the Bachem Group and get inspired by our exciting work environment at our location inVionnaz.

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