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

Join a Leader in Life Sciences Innovation

At Techfirm Engineering, we are committed to shaping the future of Life Sciences. We seek individuals with extensive experience in GMP-regulated manufacturing, particularly within a biotechnology setting. If you possess hands-on experience in Upstream Processing (USP), Downstream Processing (DSP), cell culture, fermentation, or purification, and thrive in a highly regulated, digital, and fully paperless production environment, we want to hear from you.

Your Mission

As a vital member of our production team, you will be tasked with performing and monitoring GMP-compliant manufacturing activities in a biotechnology or pharmaceutical production environment. Collaborating closely with cross-functional teams such as Manufacturing, Quality Assurance, Quality Control, Engineering, and others, you will ensure that all activities are executed safely, efficiently, and in adherence to strict GMP and quality standards.

Key Responsibilities

• Conduct hands-on manufacturing activities in a GMP-regulated environment.
• Execute manufacturing processes in accordance with approved procedures, SOPs, batch records, and GMP requirements.
• Engage in Upstream Processing (USP) and/or Downstream Processing (DSP).
• Support cell culture, fermentation, and biotechnological production processes.
• Manage purification and downstream processing activities where applicable.
• Operate, monitor, and control production equipment and manufacturing systems.
• Follow established procedures ensuring safety and compliance with GMP requirements.
• Perform in-process controls, sampling, and routine production checks.
• Accurately and timely record manufacturing activities in a fully paperless environment.
• Utilize digital manufacturing and documentation systems effectively.
• Support the investigation of deviations and quality-related events.
• Maintain compliance with GMP, EHS, data integrity, and internal quality standards.
• Foster cleanliness and compliance within the manufacturing area.
• Collaborate with various teams to enhance manufacturing processes and workflows.

Your Profile

• Professional experience in Manufacturing/Production within a regulated environment.
• Background in biotechnology is highly desirable; experience in pharmaceutical manufacturing will be considered.
• Hands-on experience in Upstream Processing (USP) and/or Downstream Processing (DSP).
• Proficiency in navigating multiple digital manufacturing systems and tools.
• Experience in paperless manufacturing environments is advantageous.
• Familiarity with Syncade and DeltaV systems is a plus.
• English proficiency at a minimum B1 level, both written and spoken.

What We Offer

• Over 25 years of expertise in the Swiss industrial ecosystem.
• 100% Swiss-headquartered with local implementation.
• A multicultural, approachable environment emphasizing collaboration and respect.
• Close interaction among consultants, clients, and project teams.
• Project selection aligned with your skills, experience, and career ambitions.
• Long-term, impactful industrial projects across various sectors.
• Exposure to modern GMP digital and paperless manufacturing processes.
• A focus on well-being and professional development.
• An inclusive workplace that promotes diversity and equal opportunities.