- Singapore Singapore
Kerja Sepenuh Masa Site Quality Head Singapore, Gaji tinggi SGD 27,800 di THERMO FISHER BIOPHARMA SERVICES PTE. LTD. - Maukerja
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Business Job Title: Site Quality Director Singapore
Group/Division: Pharma Services Group / Drug Product Division - Singapore Site
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!
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit
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Group/Division: Pharma Services Group / Drug Product Division - Singapore Site
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!
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit
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