Technical Author — Bachem AG
- Location
- Vionnaz
- Contract
- full-time
- Posted
- 2 days ago
Role overview
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.
- 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% .
- Your key responsibilities
- Create, review, and maintain GMP documentation supporting manufacturing operations and technology transfer activities.
- 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.
Main responsibilities
- 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.
Key requirements
- 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.
Application process
- 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.
Company and context
- 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?
Additional details
- Proactive team player with strong organizational and communication skills;
- Opportunities for professional development and continuing professional development. A corporate culture based on collaboration, innovation and excellence.
Notes and original content
- Your Profile
- Opportunities for professional development and continuing professional development.
- A corporate culture based on collaboration, innovation and excellence.
Questions about this listing
What salary does Bachem AG offer for this role?
Bachem AG lists CHF 71'000 - 107'500 gross per year for this position in Vionnaz. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Bachem AG offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Bachem AG during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Valais?
EU/EFTA residents living in the border zone of the country adjoining Canton Valais can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Valais's cantonal migration office or with HR during the application.
How do I apply for this position at Bachem AG?
Use the "Apply now" button on this page — it links directly to Bachem AG's original listing at careers.bachem.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
