Process Engineer – Biotech/Pharma/Chemistry (M/W/D)
Location: Bern, Switzerland (on-site, 100%)
Start Date: ASAP
About the Role
We are seeking a talented Process Engineer with fluency in German to join our team. In this role, you will support equipment upgrades and modifications, ensuring a smooth implementation process, compliance with Good Manufacturing Practices (GMP), and optimal process performance. You will collaborate closely with R&D, Manufacturing, QA, and Validation teams, making your language skills essential for effective communication with local stakeholders.
Your Responsibilities
- Plan, implement, and support equipment changes or upgrades in GMP-regulated environments.
- Participate in technology transfer and scale-up involving new or modified equipment.
- Perform risk assessments, impact analyses, and change controls for equipment modifications.
- Update and maintain process documentation such as SOPs, batch records, and qualification protocols.
- Monitor and analyze process performance before and after equipment changes.
- Troubleshoot process or equipment issues and propose corrective actions (CAPA).
- Support equipment qualification and process validation (IQ/OQ/PQ).
- Communicate effectively in German and English with internal teams, suppliers, and regulatory bodies.
Your Profile
Education:
- Bachelor’s or Master’s degree in Chemistry, Chemical Engineering, Biotechnology, or a related field.
Experience:
- 2–3 years of experience in chemical, biotech, or pharmaceutical manufacturing environments.
- Practical experience with equipment changes, upgrades, or installations.
- Knowledge of upstream and/or downstream processes (fermentation, purification, chromatography, filtration).
- Understanding of GMP requirements and regulatory compliance.
- Strong analytical and problem-solving skills.
- Excellent communication skills in German (mandatory) and English.
- Ability to work collaboratively in cross-functional teams.
Skills:
- Experience in equipment qualification and validation (IQ/OQ/PQ).
- Familiarity with PAT, QbD, or continuous improvement methodologies.
- Experience in technology transfer or process optimization projects.
- Knowledge of process monitoring tools and statistical analysis software (e.g., JMP, Minitab).
Why Join TechFirm Life Sciences?
- Play a key role in equipment upgrades and process improvements in a growing biotech/pharma environment.
- Gain exposure to innovative technologies and foster cross-functional collaboration.
- Enjoy career development opportunities within a dynamic, international company.
- Receive competitive compensation and benefits.
Interested?
If this sounds like your next professional challenge, we’d be delighted to hear from you!
Apply online using the form below. Please note that only applications matching the job profile will be considered.