Thermo Fisher Scientific
Site Quality Head Singapore
Get notified of more jobs like this · No spam, ever
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
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
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
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 acting as 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.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
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.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Location