Production Operator – GMP / Biotech Manufacturing (m/f/d)

Tech'Firm Industrie AG; Bern; On-site; CHF 70,000 - 90,000; Full time

Benefits offered by this job

Swiss HR policies and benefits

Long-term projects in Life Sciences

Collaborative team environment

Professional growth opportunities

Digital, paperless operations

Job summary

Techfirm Engineering is seeking a Production Operator to perform GMP‑regulated manufacturing activities in Bern, within a biotech/pharma production environment. You will work in a fully digital, paperless setting and collaborate across Manufacturing, QA, QC, Engineering, and MSAT to ensure compliant, efficient operations.

The role requires hands‑on experience in Upstream/Downstream Processing, cell culture, fermentation or purification, and familiarity with digital systems like Syncade or

Qualifications

• Professional experience in Manufacturing/Production within a regulated industrial environment.
• Experience in a biotechnology environment is highly desirable.
• Experience in pharmaceutical manufacturing may also be considered.
• Hands-on experience in Upstream Processing (USP) and/or Downstream Processing (DSP).

Responsibilities

• Perform hands-on manufacturing and production activities in a GMP-regulated environment.
• Execute manufacturing processes in accordance with approved procedures, SOPs, batch records and GMP requirements.
• Perform activities within Upstream Processing (USP) and/or Downstream Processing (DSP) areas.
• Support and perform manufacturing activities related to cell culture, fermentation and biotechnological production processes.
• Perform and monitor purification and downstream processing activities where applicable.
• Operate, monitor and control production equipment and manufacturing systems.
• Follow established procedures and ensure that all manufacturing activities are performed safely and in compliance with GMP requirements.
• Perform in-process controls, sampling and routine production checks according to applicable procedures.
• Ensure accurate and timely recording of manufacturing activities within the fully paperless production environment.
• Use digital manufacturing and documentation systems to execute and document production activities.
• Navigate efficiently between different digital systems and production tools.
• Support the management and investigation of deviations and other quality-related events.
• Ensure compliance with GMP, EHS, data integrity and internal quality standards.
• Maintain a high level of cleanliness and compliance within the manufacturing area.
• Collaborate closely with Manufacturing, QA, QC, Engineering, MSAT and other support functions.
• Participate in continuous improvement activities related to manufacturing processes and workflows.

Skills

Manufacturing experience

GMP knowledge

Biotech environment experience

Digital systems

Paperless manufacturing

Syncade knowledge

DeltaV knowledge

English (B1)

Education

Swiss VET Diploma or equivalent

Tools

DeltaV

Syncade

Job description

Production Operator – GMP / Biotech Manufacturing (m/f/d)

Tech'Firm Industrie AG Vacant since : 10.09.2026 Number of jobs : 1 3004 Bern (BE) 100% Immediately Permanent

Shape the future of Life Sciences with Techfirm Engineering

Techfirm Engineering is looking for a Production Operator with solid experience in GMP-regulated manufacturing, ideally within a biotechnology environment.

Do you have hands‑on experience in Upstream Processing (USP), Downstream Processing (DSP), cell culture, fermentation or purification?Are you comfortable working in a highly regulated, digital and fully paperless production environment?

Then this could be the right opportunity for you.

Your Mission

As a Production Operator, you will be responsible for carrying out and monitoring GMP‑compliant manufacturing activities within a biotechnology or pharmaceutical production environment.

You will work closely with Manufacturing, Quality Assurance, Quality Control, Engineering and other support functions to ensure that production activities are performed safely, efficiently and in accordance with applicable GMP and quality requirements.

Depending on your background and the production area, you may be involved in Upstream Processing (USP), Downstream Processing (DSP), cell culture, fermentation, purification and other biotechnological manufacturing processes.

Key Responsibilities

• Perform hands‑on manufacturing and production activities in a GMP-regulated environment.
• Execute manufacturing processes in accordance with approved procedures, SOPs, batch records and GMP requirements.
• Perform activities within Upstream Processing (USP) and/or Downstream Processing (DSP) areas.
• Support and perform manufacturing activities related to cell culture, fermentation and biotechnological production processes.
• Perform and monitor purification and downstream processing activities where applicable.
• Operate, monitor and control production equipment and manufacturing systems.
• Follow established procedures and ensure that all manufacturing activities are performed safely and in compliance with GMP requirements.
• Perform in‑process controls, sampling and routine production checks according to applicable procedures.
• Ensure accurate and timely recording of manufacturing activities within the fully paperless production environment.
• Use digital manufacturing and documentation systems to execute and document production activities.
• Navigate efficiently between different digital systems and production tools.
• Support the management and investigation of deviations and other quality‑related events.
• Ensure compliance with GMP, EHS, data integrity and internal quality standards.
• Maintain a high level of cleanliness and compliance within the manufacturing area.
• Collaborate closely with Manufacturing, QA, QC, Engineering, MSAT and other support functions.
• Participate in continuous improvement activities related to manufacturing processes and workflows.

Your Profile

• Professional experience in Manufacturing / Production within a regulated industrial environment.
• Experience in a biotechnology environment is highly desirable.
• Experience in pharmaceutical manufacturing may also be considered.
• Hands‑on experience in Upstream Processing (USP) and/or Downstream Processing (DSP).
• Ability to work efficiently with multiple digital manufacturing systems and tools.
• Experience with paperless manufacturing environments is an advantage.
• Knowledge of Syncade is an advantage.
• Knowledge of DeltaV is an advantage.
• English: minimum B1 level, both written and spoken.

What We Offer at Techfirm

• Over 25 years on the market with strong knowledge of the Swiss industrial ecosystem.
• 100% Swiss‑headquartered company with local implementation.
• Multicultural, human‑sized environment fostering collaboration and respect.
• Close proximity between consultants, clients and project teams.
• Project selection aligned with your skills, experience and career goals.
• Long‑term, high‑value industrial projects across Life Sciences, Pharma, Biotechnology, MedTech, Energy, Transport, Construction, Chemistry and more.
• Opportunity to work on high‑impact manufacturing projects within leading Life Sciences companies.
• Exposure to modern GMP, digital and paperless manufacturing environments.
• Focus on well‑being and professional growth.
• Inclusive workplace promoting diversity and equal opportunities.

Ready to Join Us?

Please note: we can only consider Swiss or EU/EFTA nationals, or candidates holding a valid Swiss work or residence permit.

• Work location 3004 Bern (BE)
• Workload 100%
• Employment start Immediately
• Employment duration Permanent
• Qualification skilled
• Work experience More than 1 year
• Education Vocational education and training with the Swiss Federal VET Diploma or equivalent
• English Orally : Good knowledge Written : Good knowledge
• By email [e-mail]