Process Engineer / Process Engineeress

Tech'Firm Industrie AG - March 10, 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 Process Engineer who is fluent in German to join our team. In this role, you will support equipment upgrades and modifications, ensuring smooth implementation, compliance with GMP standards, and optimal process performance. You will collaborate closely with R&D, Manufacturing, QA, and Validation teams, making your proficiency in German essential for engaging 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 involving new or modified equipment.
  • Conduct 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 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?

  • Engage in key roles for equipment upgrades and process improvements within a growing biotech/pharma environment.
  • Gain exposure to innovative technologies and foster cross-functional collaboration.
  • Benefit from 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!

Contact Mathilde GEORGLER at m.georgler@techfirm.ch or apply online using the form below. Please note that only applications matching the job profile will be considered.

Location : Bern
Country : Switzerland

Application Form

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

Only pdf, Word, or OpenOffice file. Maximum file size: 3 MB.