Vionnaz
Technical Author
- 30 September 2026
- 100%
- Permanent position
- German (Basic knowledge), French (Intermediate), English (Fluent)
About the job
Bachem est une entreprise cotée en bourse, axée sur les technologies de chimie peptidique. Elle propose une gamme étendue de services pour l'industrie pharmaceutique et biotechnologique. Bachem est spécialisée dans le développement de procédés de fabrication innovants et efficaces et la production sécurisée de substances pharmaceutiques à base de peptides. Un vaste catalogue de substances biochimiques destinées à la recherche ainsi que des produits de synthèse fabriqués exclusivement pour certains clients viennent compléter cette offre. Forte de son siège en Suisse et de ses filiales en Europe et aux Etats-Unis, l'entreprise est présente sur la scène internationale et jouit de l'expérience et des compétences les plus abouties dans ce secteur industriel. Bachem place la qualité, l'innovation et le partenariat au centre de la collaboration avec ses clients.
Technical Author
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.
