Manufacturing Associate (Biopharmaceuticals, Daytime, Hillerød)

Job summary

This role is for motivated Manufacturing Associates to support biopharmaceutical production in Upstream, Downstream, and Solution Preparation during daytime hours, working only 7 days over a 14-day period.

Qualifications

• Attention to detail and proactive approach to tasks.
• Ability to communicate clearly and adapt to new digital tools.
• Trustworthy and focused, with a strong work ethic.
• Enthusiastic about working under GMP conditions.
• Comfortable with production equipment and technology.
• Understanding of process interactions is beneficial.
• Proficient in reading and understanding work instructions in English.
• Experience in pharmaceutical production or a Life Science degree is preferred; familiarity with cGMP, SOPs, chromatography, filtration, or fermentation is a plus.

Responsibilities

Schedule

• Execute and revise cGMP documentation.
• Handle and complete batch documentation.
• Conduct in-process sampling and analytical measurements.
• Execute validation protocols.
• Mix solutions for Upstream and Downstream operations.
• Perform cleaning in place (CiP) and sterilization in place (SiP) of equipment.
• Train new colleagues and report deviations.
• Participate in projects related to process optimization and continuous improvements.
• Week 1: Monday, Tuesday, Friday, Saturday, Sunday.
• Week 2: Wednesday and Thursday.
• Work hours: Day 1 (06:00 – 17:04) or Day 2 (07:45 – 18:49), with initial training from 8:00 – 16:00 for the first four weeks.