Site Quality Head Singapore Thermo Fisher Scientific - 3.4 Indianapolis, IN Job Details Full-time $201,000 - $335,000 a year 7 hours ago Qualifications Biotechnology Succession planning Recruiting from diverse places Team leadership Pharmaceutical regulatory compliance Talent management Presentations for conferences or internal meetings GMP Quality improvement leadership Inclusive hiring practices Inclusive leadership practices Team development Talent pipeline development Pharmaceutical company experience Decision making Quality assurance experience within pharmaceutical industry Cleanroom experience Quality control experience within pharmaceutical industry Sterile products production Talent career development Senior level Managing product quality assurance teams Leadership Communication skills Senior leadership Pharmaceutical manufacturing facility experience 10 years Full Job Description Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP)

Safety Standards, Cleanroom:

no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed,

Office Job Description Business Job Title:

Site Quality Director Singapore Group/Division:

Pharma Services Group / Drug Product Division - Singapore Site This role is based in Singapore, we are open to candidates who are willing to relocate.

Position Summary:

As the Site Quality Director, you lead the CDMO Quality and Regulatory team, ensuring outstanding quality standards and compliance across our aseptic operations. This outstanding opportunity allows you to champion a culture of excellence and innovation, strictly adhering to regulatory guidelines and GXP compliance requirements.

Key Responsibilities:

Lead and manage the Site Quality and Regulatory team, establishing and maintaining flawless quality and compliance levels. Maintain and continuously improve the site quality systems and processes. Identify, develop, and retain top-tier talent, ensuring a strong succession plan. Foster a collaborative and inclusive culture that prioritizes quality and compliance. Develop and maintain proactive relationships with regulatory authorities and clients. Maintain an independent authority for any decision impacting Quality Act as a role model, embodying Thermo Fisher values and driving groundbreaking change. Act as a member of the

DPD EU & APAC

QLT and partner across the organization with sister sites and global functions How You Can Make an

Impact:

Proven track record of 15+ years in the pharmaceutical industry including sterile drug products and aseptic operations. Preferred experience with CDMO, biotech, and vaccine production. 5+ years actings a Qualified Person is preferred. Extensive knowledge of quality structures and regulatory bodies. 10+ years of leadership experience, successfully developing high-performing teams. Outstanding communication and presentation skills, capable of engaging senior executives. Strong ability to attract, hire, and develop diverse talent. Proactive and strategic approach, skilled at moving between details and the "big picture." Learning agility with attention to detail Demonstrated ability to make calculated, high-impact quality decisions and get results. Join us to craft the future of our Quality function and make a tangible impact on global health initiatives! Compensation The salary range estimated for this position based in is S$201,000.00-S$335,000.00.