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Technical Author

Job in 1895, Vionnaz, Canton du Valais, Switzerland
Listing for: Bachem SA
Full Time position
Listed on 2026-10-04
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Quality Engineering, Validation Engineer, Regulatory Compliance Specialist
  • Pharmaceutical
    Pharmaceutical Manufacturing, Quality Engineering, Validation Engineer, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90000 - 120000 CHF Yearly CHF 90000.00 120000.00 YEAR
Job Description & How to Apply Below
Location: Vionnaz

Technical Author

Bachem SA Vacant since : 02.10.2026 Number of jobs : 1 1895 Vionnaz (VS) 100% Immediately Permanent

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 aTechnical Author (all) 100%.As a key member of Tech Ops, 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 thedigitalization 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 manufacturingdocumentation.

Your Profile Master's degree or PhD in Chemistry, Pharmaceutical Sciences, Biochemistry, Chemical Engineering, or 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? 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 in Vionnaz.

  • Work location 1895 Vionnaz (VS)
  • Workload 100%
  • Employment start Immediately
  • Employment duration Permanent
  • By online Online form
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