Responsibilities:
- Supervise daily lab operations, advanced analytical testing, and equipment systems.
- Ensure compliance with GLP, GDP, cGMP, and company standards.
- Oversee QC quality systems, regulatory readiness, and internal/external audits.
- Direct and mentor a robust QC team, managing a team up to 40 members.
- Serve as the QC subject matter expert for production, supply chain, and other key departments.
- Lead Analytical Method Transfer (AMTE) and validation projects.
- Cultivate a culture of operational excellence using Lean/Six Sigma, Right First Time (RFT), and Statistical Process Control (SPC).
- Drive fiscal responsibility through laboratory budgeting and CAPEX planning.
- Foster a proactive EHS culture to ensure a safe workplace.
- Oversee stability programs and regulatory reporting while acting as a champion for an uncompromising quality culture.
Requirements:
- Bachelor's degree or higher in Chemistry, Pharmaceutical Sciences, Microbiology, or a related scientific discipline.
- 8–10+ years of progressive QC experience within the pharmaceutical sector.
- At least 5 years of proven experience in a leadership or people-management role.
- Deep expertise in analytical chemistry, method validation, and data integrity.
- Hands-on familiarity with laboratory systems (LIMS, HPLC, GC, Empower) and cGMP/GLP environments.
Interested candidates who wish to apply for the advertised position, please click on Apply. We regret that only shortlisted candidates will be notified.
EA License No.: 01C4394 (PERSOL SINGAPORE PTE LTD)
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