- Location
- Singapore - (PSG) 31 Joo Koon Circle · Basel, Switzerland · Toronto, Canada · Dublin, Ireland · Lyon, France · Rome, Italy · London, United Kingdom · Indianapolis, Indiana, USA · Frankfurt, Germany
- Workplace
- Onsite
- Type
- Full-time
- Source
- Workday
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, OfficeJob 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.