Process Engineer / Process Engineeress

Tech'Firm Industrie AG - April 11, 2026

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. In this role, you will support equipment upgrades and modifications, ensuring smooth implementation, compliance with Good Manufacturing Practices (GMP), and optimal process performance. Collaborating closely with R&D, Manufacturing, QA, and Validation teams, your language skills will be 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 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

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 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?

  • Contribute to key equipment upgrades and process improvements in a growing biotech/pharma environment.
  • Gain exposure to innovative technologies and collaborative cross-functional projects.
  • Benefit from career development opportunities within a dynamic, international company.
  • Enjoy competitive compensation and benefits.

Interested?

If this sounds like your next professional challenge, we’d love to hear from you! Apply online using the form below. Only applications matching the job profile will be considered.

Contact: Mathilde GEORGLER – TechFirm Life Sciences : m.georgler@techfirm.ch

Location : Bern
Country : Switzerland

Application Form

Please enter your information in the following form and attach your resume (CV)

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