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 Office Hours (40/wk)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Description
As a Senior Manager of Quality at Thermo Fisher Scientific, you will guide strategic quality initiatives and support a culture of continuous improvement across our organization. You'll oversee quality management systems, ensure regulatory compliance, and enhance customer experience through excellent quality standards. Working closely with cross-functional teams, you'll develop and implement quality strategies that support our mission of enabling customers to make the world healthier, cleaner, and safer.
A Day in the Life
In this role, you'll manage quality assurance and quality control teams while building strong partnerships with operations, R&D, commercial teams, and customers. You'll guide process improvements through Practical Process Improvement (PPI) methodologies and risk-based approaches. Your leadership will be essential in maintaining inspection readiness, managing customer relationships, and ensuring compliance with global regulatory requirements.
As a member of the site leadership team, you'll support quality initiatives that deliver consistent product excellence while meeting business objectives. You'll develop quality professionals, lead investigations, and implement data-driven solutions that enhance our quality systems and customer satisfaction.
Keys to Success
Education:
- Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in pharmaceutical, medical device, or regulated life sciences industry
- Preferred Fields of Study: Science, Engineering, Chemistry, or related technical field
- Professional certifications desired (ASQ, Lean Six Sigma, etc.)
Experience:
- 5+ years of quality management/leadership experience
- Expert knowledge of global quality standards (ISO 13485, ISO 9001, FDA 21 CFR 820, EU MDR/IVDR)
- Strong understanding of quality management systems and GMP requirements
- Demonstrated experience leading quality investigations, CAPA, and change control processes
- Experience implementing continuous improvement initiatives
- Experience with quality tools including FMEA, Risk Analysis, and Root Cause Analysis
Knowledge, Skills, Abilities:
- Excellent project management and cross-functional leadership abilities
- Strong data analysis and problem-solving capabilities
- Excellent written and verbal communication skills
- Ability to build collaborative relationships at all levels
- Experience hosting regulatory inspections and customer audits
- Proficiency with quality management software systems
- Ability to travel up to 25-50% within the US and internationally
Compensation and Benefits
The salary range estimated for this position based in North Carolina is $118,100.00–$177,200.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
- A choice of national medical and dental plans, and a national vision plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
Work Schedule
Standard Office Hours (40/wk)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Description
As a Senior Manager of Quality at Thermo Fisher Scientific, you will guide strategic quality initiatives and support a culture of continuous improvement across our organization. You'll oversee quality management systems, ensure regulatory compliance, and enhance customer experience through excellent quality standards. Working closely with cross-functional teams, you'll develop and implement quality strategies that support our mission of enabling customers to make the world healthier, cleaner, and safer.
A Day in the Life
In this role, you'll manage quality assurance and quality control teams while building strong partnerships with operations, R&D, commercial teams, and customers. You'll guide process improvements through Practical Process Improvement (PPI) methodologies and risk-based approaches. Your leadership will be essential in maintaining inspection readiness, managing customer relationships, and ensuring compliance with global regulatory requirements.
As a member of the site leadership team, you'll support quality initiatives that deliver consistent product excellence while meeting business objectives. You'll develop quality professionals, lead investigations, and implement data-driven solutions that enhance our quality systems and customer satisfaction.
Keys to Success
Education:
- Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in pharmaceutical, medical device, or regulated life sciences industry
- Preferred Fields of Study: Science, Engineering, Chemistry, or related technical field
- Professional certifications desired (ASQ, Lean Six Sigma, etc.)
Experience:
- 5+ years of quality management/leadership experience
- Expert knowledge of global quality standards (ISO 13485, ISO 9001, FDA 21 CFR 820, EU MDR/IVDR)
- Strong understanding of quality management systems and GMP requirements
- Demonstrated experience leading quality investigations, CAPA, and change control processes
- Experience implementing continuous improvement initiatives
- Experience with quality tools including FMEA, Risk Analysis, and Root Cause Analysis
Knowledge, Skills, Abilities:
- Excellent project management and cross-functional leadership abilities
- Strong data analysis and problem-solving capabilities
- Excellent written and verbal communication skills
- Ability to build collaborative relationships at all levels
- Experience hosting regulatory inspections and customer audits
- Proficiency with quality management software systems
- Ability to travel up to 25-50% within the US and internationally
Compensation and Benefits
The salary range estimated for this position based in North Carolina is $118,100.00–$177,200.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
- A choice of national medical and dental plans, and a national vision plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
See all 31+ 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.