Resume and JobRESUME AND JOB
Abbott logo

Senior Regulatory Affairs Manager

Abbott

Senior Regulatory Affairs Manager

full-timePosted: Jan 12, 2026

Job Description

Responsibilities:

  • Collaborate closely with global and local teams to develop and implement regulatory strategies for assigned projects, including business development initiatives.
  • Continuously monitor and analyze the regulatory environment in China as well as major global agencies (FDA, EMA, PMDA). Translate insights into innovative and actionable regulatory strategy.
  • Build strong relationships with internal stakeholders across Regulatory, CMC, Clinical Operations, Medical, Quality, Business Units, Market Access, and Commercial teams. Integrate regulatory intelligence and business insights into strategic decision-making. Provide regulatory support for Abbott’s planning in business, market access, commercial activities, and quality assessments.
  • Represent Abbott in interactions with regulatory authorities, industry associations, and working groups to support advocacy initiatives aligned with company priorities. Lead and maintain effective communication with regulatory agencies and external consultants.

Supervisory/Management Responsibilities:

Direct Reports:      0-2

Minimum Education:

  • A Master’s degree or above in pharmacy, biology, chemistry, pharmacology or related life sciences is required

Minimum Experience/Training Required:

  • Industry experiences: A minimum of 8 years’ experience required in Regulatory
  • Position experiences:
  • Having experience interfacing with government regulatory agencies and proven skill at developing and implementing successful China regulatory strategies.
  • Deep expertise with global regulatory frameworks (NMPA, FDA, EU/EMA, PMDA, etc.) .
  • Prior experience supporting drug development lifecycle—from development through submission and post-approval.
  • Strong analytical capabilities to assess complex regulatory information and translate it into strategic recommendations.
  • Excellent communication, presentation, and interpersonal skills with the ability to influence without direct authority.
  • Experience in Woman Health, Gastro, Liver, CV, Urology, CNS, Vaccine, etc.  is a plus

Locations

  • Beijing, Beijing, China

Salary

Estimated Salary Rangemedium confidence

100,000 - 160,000 CNY / yearly

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

Skills Required

  • Strong analytical capabilitiesintermediate
  • Excellent communication, presentation, and interpersonal skillsintermediate
  • Ability to influence without direct authorityintermediate

Required Qualifications

  • Master’s degree or above in pharmacy, biology, chemistry, pharmacology or related life sciences (experience)
  • Minimum of 8 years’ experience in Regulatory (experience)
  • Experience interfacing with government regulatory agencies (experience)
  • Proven skill at developing and implementing successful China regulatory strategies (experience)
  • Deep expertise with global regulatory frameworks (NMPA, FDA, EU/EMA, PMDA) (experience)
  • Prior experience supporting drug development lifecycle (experience)
  • Experience in Woman Health, Gastro, Liver, CV, Urology, CNS, Vaccine (plus) (experience)

Responsibilities

  • Collaborate with global and local teams to develop and implement regulatory strategies
  • Monitor and analyze regulatory environment in China and major global agencies
  • Build relationships with internal stakeholders
  • Provide regulatory support for business, market access, commercial activities, and quality assessments
  • Represent Abbott in interactions with regulatory authorities, industry associations, and working groups
  • Lead and maintain communication with regulatory agencies and external consultants

Target Your Resume for "Senior Regulatory Affairs Manager" , Abbott

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

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

Check Your ATS Score for "Senior Regulatory Affairs Manager" , Abbott

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
Quiz Challenge

Answer 10 quick questions to check your fit for Senior Regulatory Affairs Manager @ Abbott.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.

Abbott logo

Senior Regulatory Affairs Manager

Abbott

Senior Regulatory Affairs Manager

full-timePosted: Jan 12, 2026

Job Description

Responsibilities:

  • Collaborate closely with global and local teams to develop and implement regulatory strategies for assigned projects, including business development initiatives.
  • Continuously monitor and analyze the regulatory environment in China as well as major global agencies (FDA, EMA, PMDA). Translate insights into innovative and actionable regulatory strategy.
  • Build strong relationships with internal stakeholders across Regulatory, CMC, Clinical Operations, Medical, Quality, Business Units, Market Access, and Commercial teams. Integrate regulatory intelligence and business insights into strategic decision-making. Provide regulatory support for Abbott’s planning in business, market access, commercial activities, and quality assessments.
  • Represent Abbott in interactions with regulatory authorities, industry associations, and working groups to support advocacy initiatives aligned with company priorities. Lead and maintain effective communication with regulatory agencies and external consultants.

Supervisory/Management Responsibilities:

Direct Reports:      0-2

Minimum Education:

  • A Master’s degree or above in pharmacy, biology, chemistry, pharmacology or related life sciences is required

Minimum Experience/Training Required:

  • Industry experiences: A minimum of 8 years’ experience required in Regulatory
  • Position experiences:
  • Having experience interfacing with government regulatory agencies and proven skill at developing and implementing successful China regulatory strategies.
  • Deep expertise with global regulatory frameworks (NMPA, FDA, EU/EMA, PMDA, etc.) .
  • Prior experience supporting drug development lifecycle—from development through submission and post-approval.
  • Strong analytical capabilities to assess complex regulatory information and translate it into strategic recommendations.
  • Excellent communication, presentation, and interpersonal skills with the ability to influence without direct authority.
  • Experience in Woman Health, Gastro, Liver, CV, Urology, CNS, Vaccine, etc.  is a plus

Locations

  • Beijing, Beijing, China

Salary

Estimated Salary Rangemedium confidence

100,000 - 160,000 CNY / yearly

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

Skills Required

  • Strong analytical capabilitiesintermediate
  • Excellent communication, presentation, and interpersonal skillsintermediate
  • Ability to influence without direct authorityintermediate

Required Qualifications

  • Master’s degree or above in pharmacy, biology, chemistry, pharmacology or related life sciences (experience)
  • Minimum of 8 years’ experience in Regulatory (experience)
  • Experience interfacing with government regulatory agencies (experience)
  • Proven skill at developing and implementing successful China regulatory strategies (experience)
  • Deep expertise with global regulatory frameworks (NMPA, FDA, EU/EMA, PMDA) (experience)
  • Prior experience supporting drug development lifecycle (experience)
  • Experience in Woman Health, Gastro, Liver, CV, Urology, CNS, Vaccine (plus) (experience)

Responsibilities

  • Collaborate with global and local teams to develop and implement regulatory strategies
  • Monitor and analyze regulatory environment in China and major global agencies
  • Build relationships with internal stakeholders
  • Provide regulatory support for business, market access, commercial activities, and quality assessments
  • Represent Abbott in interactions with regulatory authorities, industry associations, and working groups
  • Lead and maintain communication with regulatory agencies and external consultants

Target Your Resume for "Senior Regulatory Affairs Manager" , Abbott

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

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

Check Your ATS Score for "Senior Regulatory Affairs Manager" , Abbott

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
Quiz Challenge

Answer 10 quick questions to check your fit for Senior Regulatory Affairs Manager @ Abbott.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.