GMP Biotech Production Operator – Digital, Paperless

Tech'Firm Industrie AG; Bern; In loco; CHF 70.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Swiss HR policies and benefits

Long-term projects in Life Sciences

Collaborative team environment

Professional growth opportunities

Digital, paperless operations

Descrizione del lavoro

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

Competenze

• 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).

Mansioni

• 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.

Conoscenze

Manufacturing experience

GMP knowledge

Biotech environment experience

Digital systems

Paperless manufacturing

Syncade knowledge

DeltaV knowledge

English (B1)

Formazione

Swiss VET Diploma or equivalent

Strumenti

DeltaV

Syncade

Descrizione del lavoro

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