QC Analyst – In Process Control (Shift Role)

About the role

BioMarin is seeking a QC Analyst to join its In‑Process Control team in a newly 5S‑certified analytical laboratory. The role operates on a 4‑cycle shift pattern, providing critical analytical and microbiological testing for both drug substance and drug product manufacturing in a GMP environment.

Key responsibilities

• Perform in‑process analytical testing to support continuous manufacturing operations.
• Conduct microbiological testing of in‑process samples.
• Test incoming raw materials and packaging components to ensure suitability for downstream processes.
• Maintain compliance with regulatory and GMP standards while following 5S and standard‑work practices.
• Participate in continuous‑improvement activities within the QC team.

Required profile

• High level of initiative, energy, and motivation.
• Strong organisational abilities and attention to detail.
• Flexibility to work a rotating 4‑cycle shift schedule.

Required skills

What we offer

• Exposure to both drug substance and drug product manufacturing.
• Opportunity to work in a fast‑paced, highly compliant GMP environment.
• Collaboration with a high‑performing, multi‑skilled QC team.