Technical Author Peptide Manufacturing (a), 100% (Temp. 12 months)

To strengthen the existing team in our active ingredient production, we are seeking a committed Technical Author Peptide Manufacturing (a), 100% (temporary for 12 months with a prospect of permanent employment) as soon as possible.
You will be responsible for writing production-relevant GMP documents and will specialise in one production unit (Manufacturing Cluster) in this role.

Your tasks

• Writing, updating, and optimising manufacturing instructions (MBPRs), SOPs, logbooks, and risk analyses (FMEAs) for the Peptide Manufacturing area.
• Ensuring formal and content quality of documents according to GMP and internal guidelines.
• Implementing changes to Master Batch Records (MBRs) in the MES (PAS-X) in close cooperation with producers.
• Further developing and harmonising document templates and standards to increase efficiency in document creation.
• Close collaboration with the assigned Peptide Manufacturing Cluster and building a solid understanding of manufacturing processes, equipment, and workflows.
• Active participation in process alignments, shopfloor inspections, and exchanges with operators, production leaders, and chemists to ensure precise and practical documentation.
• Compliance with all relevant GMP, HSE, and compliance requirements.
• Ensuring correct implementation of requirements in manufacturing instructions, SOPs, and risk analyses.
• Supporting internal and external audits by providing relevant documents and information.
• Active contribution to strengthening the GMP and HSE culture within the team and production environment.

Your profile

• Completed university degree in chemistry with a doctorate or a degree in natural sciences supplemented by professional experience in the pharmaceutical environment
• German at native speaker level as well as excellent English skills
• Proficiency in common MS Office tools
• Interest and enjoyment in creating production-related GMP documents
• Interest in practical workflows in production operations
• Ability to clearly present complex chemical processes and technical contexts
• Precise working style
• Ability to work independently or in a team depending on the situation
• Strong communication and coordination skills
• Interest in learning to create Master Batch Records (MBR) in Bachem’s Manufacturing Execution System (MES) (PAS-X) or experience in MBR design in an MES is advantageous

Our offer:

• A dynamic and rapidly growing work environment with internal development and training opportunities
• Flexible working hours with the possibility of home office and option to take additional holidays with reduced working hours
• Company daycare centre on the Bachem Campus Bubendorf
• 60% pension fund contribution by Bachem AG as well as the possibility of additional voluntary pension provision with our savings plan
• Access to benefit platforms with discounts from external partners
• Fresh, healthy, and varied food in our staff restaurant
• Various free sports activities on the Bachem Campus

Would you like to drive innovation forward with us?

Have we piqued your interest? Then we look forward to receiving 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!