Technical Author Peptide Manufacturing (a), 100% (Temp. 12 Monate) — Bachem AG
- Location
- Bubendorf
- Contract
- full-time
- Posted
- 2 days ago
Role overview
In order to strengthen the existing team in our drug production, we are looking for a dedicated Technical Author Peptide Manufacturing (a), 100% (temporarily for 12 months with a view to acquisition) at the earliest possible time.
They are responsible for writing production-relevant GMP documents and in this role are specialized in a production unit (manufacturing cluster). Their tasks
Writing, updating and optimizing manufacturing regulations (MBPRs), SOPs, logbooks and risk analyses (FMEAs) for peptide manufacturing.
- In order to strengthen the existing team in our drug production, we are looking for a dedicated Technical Author Peptide Manufacturing (a), 100% (temporarily for 12 months with a view to acquisition) at the earliest possible time.
- They are responsible for writing production-relevant GMP documents and in this role are specialized in a production unit (manufacturing cluster). Their tasks
- Completed university degree in chemistry with a doctorate or a study of natural sciences supplemented by professional experience in the pharmaceutical environment
- German at mother tongue level and excellent English skills Mastery of common MS Office tools
Key requirements
- Completed university degree in chemistry with a doctorate or a study of natural sciences supplemented by professional experience in the pharmaceutical environment
- German at mother tongue level and excellent English skills Mastery of common MS Office tools
- Interest and pleasure in the creation of production-related GMP documents
- Interest in practical processes in the production plant
- Ability to understand complex chemical processes and technical relationships Precise operation
- Ability to work independently or in a team due to the situation
- Strong communication and coordination capabilities
- Interested in learning to create Master Batch Records (MBR) in the Manufacturing Execution System (MES) of Bachem (PAS-X).
- Experience in MBR design in an MES advantageous Our offer:
- A dynamic and rapidly growing working environment with internal development and further education opportunities
- Flexible working hours with the option of home office and the option to purchase additional holidays with reduced workload
- Company-internal KITA on the Bachem Campus Bubendorf
Application process
- Then we look forward to your complete application documents via our application portal.
- Learn more about the Bachem Group and be inspired by our inspiring working environment at our location in Bubendorf!
Additional details
- They are responsible for writing production-relevant GMP documents and in this role are specialized in a production unit (manufacturing cluster).
- German at mother tongue level and excellent English skills Mastery of common MS Office tools
- Ability to understand complex chemical processes and technical relationships
- Experience in MBR design in an MES advantageous
Notes and original content
- Their tasks
- Your profile
- German at mother tongue level and excellent English skills
- Mastery of common MS Office tools
- Precise operation
Questions about this listing
What salary does Bachem AG offer for this role?
Bachem AG lists CHF 72'500 - 110'500 gross per year for this position in Bubendorf. 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 Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel 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 Basel'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.
