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Salary
≈ $75k – $191k per year (Estimated)
Location
In office (Switzerland)
Seniority
Middle · 3+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 11, 2026. First seen by Alion on Sep 29, 2026.

Overview
Company
Impact
Profile match
Bachem is a Swiss contract development and manufacturing company headquartered in Bubendorf near Basel, producing peptides and oligonucleotides as active pharmaceutical ingredients for pharmaceutical and biotechnology customers. Founded in 1971 and listed on the SIX Swiss Exchange, it supports clients from research and clinical development to commercial supply, with sites in Switzerland, Europe, the US and Asia, including Vista and Torrance in California. It hires process specialists, quality control and validation staff, laboratory technicians, plant engineers, accountants and SAP specialists, mainly in Switzerland and California.

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?

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.

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