Production Operator / Production Operatoress

Shape the Future of Life Sciences with Techfirm Engineering

Techfirm Engineering is seeking a skilled Production Operator with substantial experience in GMP-regulated manufacturing, ideally within the biotechnology sector. If you possess hands-on experience in Upstream Processing (USP), Downstream Processing (DSP), cell culture, fermentation, or purification, and are comfortable operating in a highly regulated, digital, and fully paperless production environment, this opportunity may be perfect for you.

Your Mission

As a Production Operator, you will be tasked with carrying out and monitoring GMP-compliant manufacturing activities within a biotechnology or pharmaceutical production environment. You will collaborate closely with Manufacturing, Quality Assurance, Quality Control, Engineering, and other support functions to ensure that all production activities are conducted safely, efficiently, and in alignment with applicable GMP and quality standards.

Depending on your background and the specific production area, your role may involve:

• 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 according to approved procedures, SOPs, batch records, and GMP requirements.
• Conduct activities within Upstream Processing (USP) and/or Downstream Processing (DSP) areas.
• Support and engage in manufacturing activities related to cell culture, fermentation, and biotechnological production processes.
• Execute and monitor purification and downstream processing activities as necessary.
• Operate, monitor, and control production equipment and manufacturing systems.
• Adhere to established procedures to 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.
• Utilize digital manufacturing and documentation systems to execute and document production activities.
• Efficiently navigate between various digital systems and production tools.
• Assist in 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 standard of cleanliness and compliance within the manufacturing area.
• Collaborate closely with Manufacturing, QA, QC, Engineering, MSAT, and other support functions.
• Participate in continuous improvement initiatives 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; pharmaceutical manufacturing experience will also be considered.
• Hands-on experience in Upstream Processing (USP) and/or Downstream Processing (DSP).
• Proficiency in utilizing multiple digital manufacturing systems and tools.
• Experience with paperless manufacturing environments is an advantage.
• Knowledge of Syncade and DeltaV is a plus.
• English language skills: minimum B1 level, both written and spoken.

What We Offer at Techfirm

• Over 25 years of experience in the Swiss industrial ecosystem.
• 100% Swiss-headquartered company with local implementation.
• A multicultural, human-sized environment that fosters collaboration and respect.
• Close proximity between consultants, clients, and project teams.
• Project selection aligned with your skills, experience, and career aspirations.
• Long-term, high-value industrial projects across various sectors, including Life Sciences, Pharma, Biotechnology, MedTech, Energy, Transport, Construction, and Chemistry.
• Opportunities to engage in impactful manufacturing projects within leading Life Sciences companies.
• Exposure to modern GMP, digital, and paperless manufacturing environments.
• A strong emphasis on employee well-being and professional development.
• An inclusive workplace that promotes diversity and equal opportunity.

Ready to Join Us?

If this opportunity resonates with you, apply online using the form below. Please note: Only applications matching the job profile will be considered.