Quality Manager Jobs at Thermo Fisher Scientific with Visa Sponsorship
Quality Manager jobs at Thermo Fisher Scientific sit at the intersection of scientific rigor and regulatory compliance, spanning manufacturing, laboratory operations, and supply chain functions. Thermo Fisher has a consistent track record of sponsoring international talent for quality-focused roles across its global network of sites.
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Get Access To All JobsWork 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 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.
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.
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 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.
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.
See all Quality Manager Jobs at Thermo Fisher Scientific
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Quality Manager Jobs at Thermo Fisher Scientific.
Get Access To All JobsTips for Finding Quality Manager Jobs at Thermo Fisher Scientific
Align your credentials to FDA-regulated environments
Thermo Fisher's quality teams operate under FDA, ISO 13485, and GMP frameworks. Certifications like CQM, CQE, or ASQ credentials signal direct readiness and reduce the employer's onboarding risk for a sponsored hire.
Target site-level roles not just corporate postings
Thermo Fisher's Quality Manager openings are often tied to specific manufacturing or laboratory sites. Filtering by location in your search surfaces roles with active headcount needs, where local hiring managers have more direct influence over sponsorship decisions.
Clarify your OPT or CPT status early in interviews
If you're on F-1 OPT, raise your authorization timeline in the first substantive conversation. Quality Manager roles involve regulatory accountability, so hiring managers need lead time to plan an H-1B petition around your work authorization expiration.
Understand how PERM affects your Green Card timeline
Thermo Fisher sponsors EB-2 and EB-3 Green Cards for quality roles, but PERM labor certification adds 12 to 18 months before USCIS adjudication begins. Factor this into your long-term planning if permanent residence is your goal.
Use Migrate Mate to find actively sponsoring Quality Manager roles
Not every Quality Manager posting at Thermo Fisher is tied to active sponsorship capacity. Migrate Mate filters specifically for visa-sponsoring employers, so you're applying to roles where international candidates are genuinely being considered.
Prepare for TN eligibility if you hold Canadian or Mexican citizenship
Quality Manager roles can qualify under the TN visa category for Canadian and Mexican citizens. Confirm with USCIS criteria that your specific job description maps to an eligible profession before relying on this pathway during offer negotiations.
Frequently Asked Questions
Does Thermo Fisher Scientific sponsor H-1B visas for Quality Managers?
Yes. Thermo Fisher Scientific has a well-established pattern of sponsoring H-1B visas for Quality Manager roles, particularly across its manufacturing and laboratory operations. Because Quality Manager positions involve regulatory compliance and specialized knowledge, they typically satisfy the H-1B specialty occupation standard. Your employer will file the petition with USCIS, but you should confirm sponsorship intent early in the interview process.
How do I apply for Quality Manager jobs at Thermo Fisher Scientific?
Applications go through Thermo Fisher's careers portal, where roles are posted by site and function. Search for Quality Manager openings filtered by location, since many roles are tied to specific manufacturing or laboratory facilities. Migrate Mate also lists Thermo Fisher's sponsoring Quality Manager roles in one place, which helps you identify positions where international candidates are actively being considered before you apply.
Which visa types does Thermo Fisher Scientific commonly use for Quality Manager roles?
Thermo Fisher sponsors H-1B visas as the primary nonimmigrant pathway for Quality Managers. The company also supports F-1 OPT and CPT for candidates already in the U.S. on student visas, and offers TN visa sponsorship for Canadian and Mexican nationals in eligible roles. For long-term employees, Thermo Fisher pursues EB-2 and EB-3 Green Card sponsorship through the PERM labor certification process.
What qualifications does Thermo Fisher Scientific expect for Quality Manager candidates?
Thermo Fisher typically expects a bachelor's degree in a scientific or engineering discipline, combined with direct experience in GMP, ISO 13485, or FDA-regulated manufacturing environments. Quality management certifications such as CQM or CQE from ASQ strengthen your application. For senior roles, experience managing CAPA processes, supplier quality, or regulatory submissions is often required rather than preferred.
How do I time my H-1B application when starting a Quality Manager role at Thermo Fisher?
H-1B petitions are subject to an annual cap with a registration window in March and an October 1 start date. If you're on F-1 OPT, confirm whether your OPT expiration gives you enough runway to bridge to an H-1B approval. USCIS premium processing reduces adjudication to around 15 business days, which Thermo Fisher may use when your work authorization timeline is tight.