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Sr Manager, Regulatory Affairs

Thermo Fisher Scientific

Healthcare Jobs

Sr Manager, Regulatory Affairs

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. Alongside clinical research through our PPD® clinical research portfolio, our work in evidence-based solutions specializes in generating the evidence needed to optimize the commercial potential of our biopharma and biotech customers’ products. Your determination to demonstrate effectiveness, safety and the value of these products will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

St. Louis, Missouri Drug Substance Division

Discover Impactful Work:

Join our dynamic team and play a vital role in delivering life-changing therapies! Your work will be instrumental in ensuring compliance and supporting our mission to make the world healthier, cleaner, and safer.

A day in the Life:

  • Serve as the primary contact for Site Regulatory Affairs
  • Coordinate regulatory assessments and filing management
  • Provide strategic regulatory support to project teams

Keys to Success:

  • Outstanding leadership and collaboration skills
  • Proven ability to manage staff and regulatory processes
  • Dedication to achieving flawless compliance

Education

  • Bachelor’s degree in a scientific or related field is mandatory.

Experience

  • 10+ years in a Quality role in a cGMP environment
  • 5+ years managing people
  • 5+ years regulatory experience in the biopharmaceutical industry

Knowledge, Skills, Abilities

  • Strong understanding of global regulatory requirements
  • Highly effective verbal and written communication skills
  • Collaborative team member with strong communication abilities

Physical Requirements / Work Environment

Office and laboratory settings, requiring occasional travel and adherence to safety protocols.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

 

OTHER

  • Relocation assistance may be provided.
  • Must be legally authorized to work in the United States now and in the future, without sponsorship.
  • Must be able to pass a comprehensive background check, which includes a drug screening.

Locations

  • St. Louis, Missouri, United States of America

Salary

Estimated Salary Rangemedium confidence

90,000 - 150,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong understanding of global regulatory requirementsintermediate
  • Highly effective verbal and written communication skillsintermediate
  • Collaborative team memberintermediate
  • Outstanding leadership and collaboration skillsintermediate

Required Qualifications

  • Bachelor’s degree in a scientific or related field (experience)
  • 10+ years in a Quality role in a cGMP environment (experience)
  • 5+ years managing people (experience)
  • 5+ years regulatory experience in the biopharmaceutical industry (experience)

Responsibilities

  • Serve as the primary contact for Site Regulatory Affairs
  • Coordinate regulatory assessments and filing management
  • Provide strategic regulatory support to project teams

Benefits

  • general: Competitive remuneration
  • general: Annual incentive plan bonus
  • general: Healthcare
  • general: Range of employee benefits
  • general: Relocation assistance may be provided

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Thermo Fisher Scientific logo

Sr Manager, Regulatory Affairs

Thermo Fisher Scientific

Healthcare Jobs

Sr Manager, Regulatory Affairs

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life – To enable our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. Alongside clinical research through our PPD® clinical research portfolio, our work in evidence-based solutions specializes in generating the evidence needed to optimize the commercial potential of our biopharma and biotech customers’ products. Your determination to demonstrate effectiveness, safety and the value of these products will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

St. Louis, Missouri Drug Substance Division

Discover Impactful Work:

Join our dynamic team and play a vital role in delivering life-changing therapies! Your work will be instrumental in ensuring compliance and supporting our mission to make the world healthier, cleaner, and safer.

A day in the Life:

  • Serve as the primary contact for Site Regulatory Affairs
  • Coordinate regulatory assessments and filing management
  • Provide strategic regulatory support to project teams

Keys to Success:

  • Outstanding leadership and collaboration skills
  • Proven ability to manage staff and regulatory processes
  • Dedication to achieving flawless compliance

Education

  • Bachelor’s degree in a scientific or related field is mandatory.

Experience

  • 10+ years in a Quality role in a cGMP environment
  • 5+ years managing people
  • 5+ years regulatory experience in the biopharmaceutical industry

Knowledge, Skills, Abilities

  • Strong understanding of global regulatory requirements
  • Highly effective verbal and written communication skills
  • Collaborative team member with strong communication abilities

Physical Requirements / Work Environment

Office and laboratory settings, requiring occasional travel and adherence to safety protocols.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

 

OTHER

  • Relocation assistance may be provided.
  • Must be legally authorized to work in the United States now and in the future, without sponsorship.
  • Must be able to pass a comprehensive background check, which includes a drug screening.

Locations

  • St. Louis, Missouri, United States of America

Salary

Estimated Salary Rangemedium confidence

90,000 - 150,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong understanding of global regulatory requirementsintermediate
  • Highly effective verbal and written communication skillsintermediate
  • Collaborative team memberintermediate
  • Outstanding leadership and collaboration skillsintermediate

Required Qualifications

  • Bachelor’s degree in a scientific or related field (experience)
  • 10+ years in a Quality role in a cGMP environment (experience)
  • 5+ years managing people (experience)
  • 5+ years regulatory experience in the biopharmaceutical industry (experience)

Responsibilities

  • Serve as the primary contact for Site Regulatory Affairs
  • Coordinate regulatory assessments and filing management
  • Provide strategic regulatory support to project teams

Benefits

  • general: Competitive remuneration
  • general: Annual incentive plan bonus
  • general: Healthcare
  • general: Range of employee benefits
  • general: Relocation assistance may be provided

Target Your Resume for "Sr Manager, Regulatory Affairs" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Sr Manager, Regulatory Affairs. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr Manager, Regulatory Affairs" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Sr Manager, Regulatory Affairs @ Thermo Fisher Scientific.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.