Manufacturing Associate (Biopharmaceutical, Night Shift)

Job summary

This role involves working as a Manufacturing Associate in biopharmaceutical production, specifically during night shifts. The position focuses on quality, teamwork, and making a significant impact in the production of medicines.

Qualifications

• Detail-oriented with a proactive approach to tasks.
• Strong communication skills and ability to learn new digital tools quickly.
• Enthusiastic about working under Good Manufacturing Practices (GMP).
• Ability to understand process flows and read work instructions in English.
• Experience in pharmaceutical production or regulated industries is preferred, or a Life Science degree.
• Familiarity with cGMP, SOPs, chromatography, filtration, or fermentation processes is a plus.
• Experience working night shifts is advantageous.

Responsibilities

Schedule

• Execute and revise cGMP documents.
• Handle and complete batch documentation.
• Conduct in-process sampling and analytical measurements.
• Prepare process equipment and execute validation protocols.
• Perform cleaning in place (CIP) of equipment.
• Train new colleagues and report deviations and safety observations.
• Participate in various projects focused on safety, process optimization, and continuous improvements.
• Work schedule includes nights with specific shifts: Night 1 (18:30 – 04:43) or Night 2 (20:05 – 06:18).
• Initial four weeks include comprehensive training from 8:00 – 16:00.

Tools

• Familiarity with digital tools and IT systems related to production processes.