Technical Author

Bachem Holding AG; Schweiz; Hybrid; EUR 116.000 - 148.000; Vollzeit

Benefits dieser Stelle

Competitive employee benefits

Professional development opportunities

Zusammenfassung

Bachem Holding AG in Vionnaz, Switzerland, seeks a Technical Author (all) 100% to create and maintain GMP manufacturing documentation, support technology transfer and new product introduction, and help digitize manufacturing records.

You will translate process knowledge into compliant records, collaborate with process scientists, labs, Manufacturing and QA, and contribute to eMBPR implementation. Fluent in French and English; German is a plus; Master’s or PhD; 3–5 years GMP experience.

Qualifikationen

• Master's degree or PhD in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related discipline.
• Strong scientific background with understanding of chemical and pharmaceutical manufacturing processes.
• 3–5 years of experience in a GMP-regulated pharmaceutical or chemical environment.
• Experience in technical writing, manufacturing documentation, technology transfer, or process development.
• Familiarity with batch record creation and document management systems.
• Excellent technical writing skills with attention to detail and a structured approach.
• Fluent in French and English (C1); German a strong asset.
• Proactive team player with good organizational and communication skills.

Aufgaben

• Create, review, and maintain GMP documentation supporting manufacturing operations and technology transfer activities.
• Prepare MBPRs, manufacturing instructions, protocols, reports, and related technical documents.
• Translate process knowledge into compliant, manufacturing-ready documentation.
• Collaborate with Process Scientists, labs, 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 and regulatory expectations.
• Contribute to eMBPR implementation and digitization of manufacturing documentation.

Kenntnisse

Technical writing

Documentation management

Team collaboration

Ausbildung

Master's degree or PhD in Chemistry / Pharmaceutical Sciences / Biochemistry / Chemical Engineering

Tools

Document management systems

Jobbeschreibung

Bachem is a world leader in the development and manufacture of peptides and oligonucleotides for the pharmaceutical industry. To strengthen our Technical Operations team in Vionnaz (Valais, Switzerland), we are looking for a Technical Author (all) 100%.

As a key member of TechOps, you will create and maintain GMP manufacturing documentation, support technology transfer and new product introduction projects, and ensure process knowledge is translated into compliant, manufacturing-ready records. You will also contribute to the implementation of eMBPR and the digitalization of manufacturing documentation.

Your key responsibilities

• Create, review, and maintain GMP documentation supporting manufacturing operations and technology transfer activities.
• Prepare Master Batch Production Records (MBPRs), manufacturing instructions, protocols, reports, and related 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 regulatory expectations.
• Contribute to the implementation of eMBPR and the standardization and digitalization of manufacturing documentation.

Your Profile

• Master's degree or PhD in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or a related discipline.
• Strong scientific background with a solid understanding of chemical and pharmaceutical manufacturing processes.
• Minimum 3 to 5 years of experience in a GMP-regulated pharmaceutical or chemical environment.
• Experience in technical writing, manufacturing documentation, technology transfer, or process development.
• 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?

Learn more about the Bachem Group and get inspired by our exciting work environment at our location in Vionnaz.