A commercial pharmaceutical manufacturer is hiring multiple QC Supervisors to lead analytical testing and product release activities within its GMP laboratory operations.

This is a hands-on leadership role where you’ll oversee a team of analysts in a fast-paced QC environment, with direct impact on batch release timelines and the opportunity to remain technically involved in analytical testing and troubleshooting.

You should apply if you have the following experience:

• 6+ years of analytical laboratory experience in a pharmaceutical or biotech environment
• 5+ years working within a GMP-regulated setting
• Strong hands-on experience with HPLC or GC, including troubleshooting
• Experience leading or mentoring analysts (Supervisor, Lead, or senior-level step-up)
• Experience with investigations (OOS, deviations) and supporting CAPAs

We aim to be an equal opportunity recruiter and we are determined to ensure that no applicant receives less favourable treatment on the grounds of gender, age, disability, religion, belief, sexual orientation, marital status, or race, or is disadvantaged by conditions or requirements.