Technical Author

Bachem is a world leader in the development and manufacture of peptides and oligonucleotides for thepharmaceutical industry. To strengthen our Technical Operations team in Vionnaz (Valais, Switzerland), we arelooking for a
Technical Author (all) 100%
.
As a key member of TechOps, you will create and maintain GMP manufacturing documentation, supporttechnology transfer and new product introduction projects, and ensure process knowledge is translated intocompliant, 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 technologytransfer activities.
Prepare Master Batch Production Records (MBPRs), manufacturing instructions, protocols, reports, andrelated 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 regulatoryexpectations.