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 fluent in German to join our dynamic team. In this role, you will play a pivotal part in supporting equipment upgrades and modifications, ensuring their smooth implementation, compliance with GMP standards, and optimal process performance. You will collaborate closely with R&D, Manufacturing, QA, and Validation teams, leveraging your language skills to effectively engage 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 analysis, and change controls for equipment modifications.
- Update and maintain process documentation (SOPs, batch records, 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
We are looking for candidates with the following qualifications:
- 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 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 benefit from cross-functional collaboration.
- Access career development opportunities in a dynamic, international company.
- Receive competitive compensation and benefits.
Interested?
If this sounds like your next professional challenge, we would love to hear from you!
Apply online using the form below. Remember, only applications matching the job profile will be considered.
For additional inquiries, please contact Mathilde GEORGLER at TechFirm Life Sciences: m.georgler@techfirm.ch.