Resume and JobRESUME AND JOB
Bristol-Myers Squibb logo

Regulatory Affair Manager

Bristol-Myers Squibb

Regulatory Affair Manager

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 21, 2025

Number of Vacancies: 1

Job Description

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. To be responsible for the regulatory activities in some ASEAN (Brunei, Malaysia, Singapore, Indonesia) by providing technical information, in order to assist in registration and compliance of BMS portfolio. A team perspective, good interpersonal skills, ability to multi-task and prioritize are critical If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • Bristol Myers Squibb is a company focused on transforming patients' lives through science
  • Offers opportunities for growth and development in various departments
  • Promotes a supportive culture with values of passion, innovation, urgency, accountability, inclusion, and integrity
  • Committed to diversity, equity, and inclusion, with transparent recruitment processes and accommodations for people with disabilities
  • Encourages global participation in clinical trials

Key Responsibilities

  • Manage regulatory activities in ASEAN countries (Brunei, Malaysia, Singapore, Indonesia)
  • Provide technical information to assist in registration and compliance of BMS portfolio
  • Ensure compliance with local and international regulatory requirements
  • Collaborate with cross-functional teams to support product development and lifecycle management

Required Qualifications

  • Bachelor's degree in a relevant field such as life sciences, pharmacy, or related discipline
  • Experience in regulatory affairs within the pharmaceutical industry

Preferred Qualifications

  • Advanced degree (Master's or PhD) in a relevant field
  • Experience with ASEAN regulatory environments (Brunei, Malaysia, Singapore, Indonesia)

Skills Required

  • Strong interpersonal skills
  • Ability to multi-task and prioritize
  • Team-oriented perspective
  • Technical knowledge in regulatory affairs
  • Effective communication and collaboration skills

Benefits & Perks

  • Competitive compensation package
  • Wide variety of benefits, services, and programs
  • Support for work-life balance and flexibility
  • Opportunities for career growth and development
  • Supportive culture promoting global participation in clinical trials
  • Reasonable workplace accommodations/adjustments for people with disabilities
  • Strong recommendation for Covid-19 vaccination and boosters

Additional Requirements

  • Willingness to work in a site-essential or site-by-design role, requiring at least 50% onsite presence
  • Ability to travel for field-based and remote-by-design roles to visit customers, patients, or business partners
  • Compliance with BMS's Covid-19 vaccination and booster recommendations

Locations

  • Singapore, Singapore

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

80,000 - 120,000 SGD / yearly

Source: ai estimated

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

Skills Required

  • Strong interpersonal skillsintermediate
  • Ability to multi-task and prioritizeintermediate
  • Team-oriented perspectiveintermediate
  • Technical knowledge in regulatory affairsintermediate
  • Effective communication and collaboration skillsintermediate

Required Qualifications

  • Bachelor's degree in a relevant field such as life sciences, pharmacy, or related discipline (experience)
  • Experience in regulatory affairs within the pharmaceutical industry (experience)

Preferred Qualifications

  • Advanced degree (Master's or PhD) in a relevant field (experience)
  • Experience with ASEAN regulatory environments (Brunei, Malaysia, Singapore, Indonesia) (experience)

Responsibilities

  • Manage regulatory activities in ASEAN countries (Brunei, Malaysia, Singapore, Indonesia)
  • Provide technical information to assist in registration and compliance of BMS portfolio
  • Ensure compliance with local and international regulatory requirements
  • Collaborate with cross-functional teams to support product development and lifecycle management

Benefits

  • general: Competitive compensation package
  • general: Wide variety of benefits, services, and programs
  • general: Support for work-life balance and flexibility
  • general: Opportunities for career growth and development
  • general: Supportive culture promoting global participation in clinical trials
  • general: Reasonable workplace accommodations/adjustments for people with disabilities
  • general: Strong recommendation for Covid-19 vaccination and boosters

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Bristol-Myers Squibb logo

Regulatory Affair Manager

Bristol-Myers Squibb

Regulatory Affair Manager

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 21, 2025

Number of Vacancies: 1

Job Description

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. To be responsible for the regulatory activities in some ASEAN (Brunei, Malaysia, Singapore, Indonesia) by providing technical information, in order to assist in registration and compliance of BMS portfolio. A team perspective, good interpersonal skills, ability to multi-task and prioritize are critical If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients' lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

About the Role/Company

  • Bristol Myers Squibb is a company focused on transforming patients' lives through science
  • Offers opportunities for growth and development in various departments
  • Promotes a supportive culture with values of passion, innovation, urgency, accountability, inclusion, and integrity
  • Committed to diversity, equity, and inclusion, with transparent recruitment processes and accommodations for people with disabilities
  • Encourages global participation in clinical trials

Key Responsibilities

  • Manage regulatory activities in ASEAN countries (Brunei, Malaysia, Singapore, Indonesia)
  • Provide technical information to assist in registration and compliance of BMS portfolio
  • Ensure compliance with local and international regulatory requirements
  • Collaborate with cross-functional teams to support product development and lifecycle management

Required Qualifications

  • Bachelor's degree in a relevant field such as life sciences, pharmacy, or related discipline
  • Experience in regulatory affairs within the pharmaceutical industry

Preferred Qualifications

  • Advanced degree (Master's or PhD) in a relevant field
  • Experience with ASEAN regulatory environments (Brunei, Malaysia, Singapore, Indonesia)

Skills Required

  • Strong interpersonal skills
  • Ability to multi-task and prioritize
  • Team-oriented perspective
  • Technical knowledge in regulatory affairs
  • Effective communication and collaboration skills

Benefits & Perks

  • Competitive compensation package
  • Wide variety of benefits, services, and programs
  • Support for work-life balance and flexibility
  • Opportunities for career growth and development
  • Supportive culture promoting global participation in clinical trials
  • Reasonable workplace accommodations/adjustments for people with disabilities
  • Strong recommendation for Covid-19 vaccination and boosters

Additional Requirements

  • Willingness to work in a site-essential or site-by-design role, requiring at least 50% onsite presence
  • Ability to travel for field-based and remote-by-design roles to visit customers, patients, or business partners
  • Compliance with BMS's Covid-19 vaccination and booster recommendations

Locations

  • Singapore, Singapore

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

80,000 - 120,000 SGD / yearly

Source: ai estimated

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

Skills Required

  • Strong interpersonal skillsintermediate
  • Ability to multi-task and prioritizeintermediate
  • Team-oriented perspectiveintermediate
  • Technical knowledge in regulatory affairsintermediate
  • Effective communication and collaboration skillsintermediate

Required Qualifications

  • Bachelor's degree in a relevant field such as life sciences, pharmacy, or related discipline (experience)
  • Experience in regulatory affairs within the pharmaceutical industry (experience)

Preferred Qualifications

  • Advanced degree (Master's or PhD) in a relevant field (experience)
  • Experience with ASEAN regulatory environments (Brunei, Malaysia, Singapore, Indonesia) (experience)

Responsibilities

  • Manage regulatory activities in ASEAN countries (Brunei, Malaysia, Singapore, Indonesia)
  • Provide technical information to assist in registration and compliance of BMS portfolio
  • Ensure compliance with local and international regulatory requirements
  • Collaborate with cross-functional teams to support product development and lifecycle management

Benefits

  • general: Competitive compensation package
  • general: Wide variety of benefits, services, and programs
  • general: Support for work-life balance and flexibility
  • general: Opportunities for career growth and development
  • general: Supportive culture promoting global participation in clinical trials
  • general: Reasonable workplace accommodations/adjustments for people with disabilities
  • general: Strong recommendation for Covid-19 vaccination and boosters

Target Your Resume for "Regulatory Affair Manager" , Bristol-Myers Squibb

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

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

Check Your ATS Score for "Regulatory Affair Manager" , Bristol-Myers Squibb

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

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Related Jobs You May Like

No related jobs found at the moment.