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 who is a German speaker to join our dynamic team. In this role, you will support equipment upgrades and modifications, ensuring smooth implementation, compliance with GMP, and optimal process performance. You will collaborate closely with our R&D, Manufacturing, QA, and Validation teams. Your fluency in German will be essential for effective communication with local teams and stakeholders.
Your Responsibilities
- Plan, implement, and support equipment changes or upgrades in GMP-regulated environments.
- Participate in technology transfer and scale-up projects involving new or modified equipment.
- Conduct risk assessments, impact analysis, and change controls for equipment modifications.
- Update and maintain process documentation, including 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.
- Able 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 tech 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 within a growing biotech/pharma environment.
- Gain exposure to innovative technologies and engage in cross-functional collaboration.
- Access career development opportunities within a dynamic, international company.
- Receive competitive compensation and benefits.
Interested?
If this opportunity aligns with your professional aspirations, we’d be delighted to hear from you!
Apply online using the form below. Only applications matching the job profile will be considered.