Manufacturing Technician (Biopharmaceuticals, Søborg)

Job summary

The role involves buffer preparation in a cGMP-regulated environment, essential for the production of biologic medicines. The position is based in a modern facility focused on preclinical, clinical, and commercial manufacturing.

Qualifications

• Experience in a GMP-regulated production environment.
• Relevant technical background such as Process Operator or Process Technologist.
• Familiarity with buffer preparation and production records.
• Knowledge of Lean, 5S, or continuous improvement practices is a plus.
• Proficient in English in a professional context.

Responsibilities

• Execute daily production activities, including batch documentation and reviews.
• Support onboarding and training of new technicians.
• Ensure compliance with regulatory and quality systems.
• Follow GMP, MPRs, and approved procedures consistently.
• Contribute ideas for continuous improvement and participate in their implementation.
• Assist with troubleshooting and production-related challenges.
• Work independently on routine and ad hoc tasks.

Skills

• Strong attention to detail and reliability in a fast-paced environment.
• Positive and flexible attitude towards new assignments.
• Ability to thrive in a dynamic production setting.

Education

• Relevant technical education or equivalent hands-on experience in biopharmaceutical production.

Tools

• Familiarity with production documentation systems such as TrackWise.