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Bristol-Myers Squibb logo

Senior Manager, Quality Systems - Change Control and Quality Risk Management Process Owner

Bristol-Myers Squibb

Senior Manager, Quality Systems - Change Control and Quality Risk Management Process Owner

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: December 3, 2025

Number of Vacancies: 1

Job Description

Own and maintain the Devens Cell Therapy site Change Control systems, including the ownership and facilitation of site Change Control Review Board. Establish and drive Change Control governance maturity plans to improve site performance through data-based analysis and integration of management review through site Quality Council. Supports the administration and maintenance of the site change control system, assuring consistency with establishing standards for local and global change control systems, as well as applicable health authority regulations. Liaise with Technical Review Board, IT change management, and QA Technical Services teams to drive technical change management solutions. Lead complex problem solving to deliver compliance focused solutions through stakeholder management with local and global teams. Build & maintain strong relationships with partner functions. Site subject matter expert on relevant quality systems and ownership of site SOPs, Work Instructions, Training documents, and business process tools. Own and maintain the Devens Cell Therapy site QRM systems, including maintenance of the site Quality Risk Register. Establish and drive QRM governance maturity plans to improve site performance through data-based analysis and integration of management review through site Quality Council. Function as site Risk Champion and collaborate with stakeholders to develop appropriate actions to resolve quality system issues and drive risk reduction initiatives. Facilitate risk assessment activities as required. Promote the development of a risk-aware culture at BMS and ensure alignment of these efforts with broader Quality initiatives. Support front room External Inspection activities as site SME on relevant Quality System elements. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities Strong working knowledge of Tech Transfer, Computer System Validation, and Commissioning and Qualification processes Strong knowledge and proven experience in applying risk management tools and methods (e.g., FMEA, PHA, HAACP, Risk Ranking and Filtering) Ability to research, understand, interpret and apply internal policies and regulatory guidelines Proficient computer skills, with knowledge of digital tools such as MS Office, and ability to learn and work with new software applications Advanced ability to interpret data & results, understand complex problems with multiple variables and critically assess and provide feedback on impact assessments and proposed actions Ability to critically review reports, interpret results, and assess and challenge technical conclusions consistent with Quality Risk Management principles Excellent verbal and technical writing skills with advanced ability to prepare written communications and present complex technical data to management with clarity and accuracy Ability to work in a fast-paced team environment and lead team and cross-functional stakeholders through changing priorities. Ability to think strategically, meet deadlines and prioritize work Ability to independently work across and influence cross-functional groups and network teams to ensure requirements are met Ability to motivate and foster a positive team environment Confident in making decisions, able to anticipate Quality issues and proactively solve problems Curious, with an ability to think critically to create innovative solutions Bachelor's degree in STEM field preferred. High school diploma/ Associates degree with equivalent combination of education and work experience may be considered. 8+ years of experience in a regulated industry, preferably with 4+ years of quality system experience including demonstrated experience with Change Control and Risk Management. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. Demonstrated proficiency with electronic system and database

About the Role/Company

  • BMS (Bristol Myers Squibb) is focused on promoting a risk-aware culture and aligning risk management efforts with broader Quality initiatives

Key Responsibilities

  • Own and maintain the Devens Cell Therapy site Change Control systems
  • Facilitate site Change Control Review Board
  • Establish and drive Change Control governance maturity plans
  • Improve site performance through data-based analysis and integration of management review
  • Support administration and maintenance of the site change control system
  • Ensure consistency with local and global change control standards and health authority regulations
  • Liaise with Technical Review Board, IT change management, and QA Technical Services teams
  • Drive technical change management solutions
  • Lead complex problem solving to deliver compliance focused solutions
  • Build & maintain strong relationships with partner functions
  • Serve as site subject matter expert on relevant quality systems
  • Own and maintain site SOPs, Work Instructions, Training documents, and business process tools
  • Own and maintain the Devens Cell Therapy site QRM systems
  • Maintain the site Quality Risk Register
  • Establish and drive QRM governance maturity plans
  • Function as site Risk Champion
  • Collaborate with stakeholders to develop actions to resolve quality system issues
  • Drive risk reduction initiatives
  • Facilitate risk assessment activities
  • Promote the development of a risk-aware culture at BMS
  • Ensure alignment of risk management efforts with broader Quality initiatives
  • Support front room External Inspection activities as site SME on relevant Quality System elements

Required Qualifications

  • Bachelor's degree in STEM field
  • High school diploma/Associates degree with equivalent combination of education and work experience
  • + years of experience in a regulated industry
  • + years of quality system experience including demonstrated experience with Change Control and Risk Management

Preferred Qualifications

  • Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing

Skills Required

  • Strong working knowledge of Tech Transfer, Computer System Validation, and Commissioning and Qualification processes
  • Strong knowledge and proven experience in applying risk management tools and methods (e.g., FMEA, PHA, HAACP, Risk Ranking and Filtering)
  • Ability to research, understand, interpret and apply internal policies and regulatory guidelines
  • Proficient computer skills, with knowledge of digital tools such as MS Office
  • Ability to learn and work with new software applications
  • Advanced ability to interpret data & results, understand complex problems with multiple variables
  • Critically assess and provide feedback on impact assessments and proposed actions
  • Ability to critically review reports, interpret results, and assess and challenge technical conclusions
  • Excellent verbal and technical writing skills
  • Advanced ability to prepare written communications and present complex technical data to management with clarity and accuracy
  • Ability to work in a fast-paced team environment and lead team and cross-functional stakeholders through changing priorities
  • Ability to think strategically, meet deadlines and prioritize work
  • Ability to independently work across and influence cross-functional groups and network teams
  • Ability to motivate and foster a positive team environment
  • Confident in making decisions, able to anticipate Quality issues and proactively solve problems
  • Curious, with an ability to think critically to create innovative solutions

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility
  • Supporting People with Disabilities

Locations

  • Devens MA, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 220,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Strong working knowledge of Tech Transfer, Computer System Validation, and Commissioning and Qualification processesintermediate
  • Strong knowledge and proven experience in applying risk management tools and methods (e.g., FMEA, PHA, HAACP, Risk Ranking and Filtering)intermediate
  • Ability to research, understand, interpret and apply internal policies and regulatory guidelinesintermediate
  • Proficient computer skills, with knowledge of digital tools such as MS Officeintermediate
  • Ability to learn and work with new software applicationsintermediate
  • Advanced ability to interpret data & results, understand complex problems with multiple variablesintermediate
  • Critically assess and provide feedback on impact assessments and proposed actionsintermediate
  • Ability to critically review reports, interpret results, and assess and challenge technical conclusionsintermediate
  • Excellent verbal and technical writing skillsintermediate
  • Advanced ability to prepare written communications and present complex technical data to management with clarity and accuracyintermediate
  • Ability to work in a fast-paced team environment and lead team and cross-functional stakeholders through changing prioritiesintermediate
  • Ability to think strategically, meet deadlines and prioritize workintermediate
  • Ability to independently work across and influence cross-functional groups and network teamsintermediate
  • Ability to motivate and foster a positive team environmentintermediate
  • Confident in making decisions, able to anticipate Quality issues and proactively solve problemsintermediate
  • Curious, with an ability to think critically to create innovative solutionsintermediate

Required Qualifications

  • Bachelor's degree in STEM field (experience)
  • High school diploma/Associates degree with equivalent combination of education and work experience (experience)
  • + years of experience in a regulated industry (experience)
  • + years of quality system experience including demonstrated experience with Change Control and Risk Management (experience)

Preferred Qualifications

  • Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing (experience)

Responsibilities

  • Own and maintain the Devens Cell Therapy site Change Control systems
  • Facilitate site Change Control Review Board
  • Establish and drive Change Control governance maturity plans
  • Improve site performance through data-based analysis and integration of management review
  • Support administration and maintenance of the site change control system
  • Ensure consistency with local and global change control standards and health authority regulations
  • Liaise with Technical Review Board, IT change management, and QA Technical Services teams
  • Drive technical change management solutions
  • Lead complex problem solving to deliver compliance focused solutions
  • Build & maintain strong relationships with partner functions
  • Serve as site subject matter expert on relevant quality systems
  • Own and maintain site SOPs, Work Instructions, Training documents, and business process tools
  • Own and maintain the Devens Cell Therapy site QRM systems
  • Maintain the site Quality Risk Register
  • Establish and drive QRM governance maturity plans
  • Function as site Risk Champion
  • Collaborate with stakeholders to develop actions to resolve quality system issues
  • Drive risk reduction initiatives
  • Facilitate risk assessment activities
  • Promote the development of a risk-aware culture at BMS
  • Ensure alignment of risk management efforts with broader Quality initiatives
  • Support front room External Inspection activities as site SME on relevant Quality System elements

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility
  • general: Supporting People with Disabilities

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Bristol-Myers Squibb logo

Senior Manager, Quality Systems - Change Control and Quality Risk Management Process Owner

Bristol-Myers Squibb

Senior Manager, Quality Systems - Change Control and Quality Risk Management Process Owner

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: December 3, 2025

Number of Vacancies: 1

Job Description

Own and maintain the Devens Cell Therapy site Change Control systems, including the ownership and facilitation of site Change Control Review Board. Establish and drive Change Control governance maturity plans to improve site performance through data-based analysis and integration of management review through site Quality Council. Supports the administration and maintenance of the site change control system, assuring consistency with establishing standards for local and global change control systems, as well as applicable health authority regulations. Liaise with Technical Review Board, IT change management, and QA Technical Services teams to drive technical change management solutions. Lead complex problem solving to deliver compliance focused solutions through stakeholder management with local and global teams. Build & maintain strong relationships with partner functions. Site subject matter expert on relevant quality systems and ownership of site SOPs, Work Instructions, Training documents, and business process tools. Own and maintain the Devens Cell Therapy site QRM systems, including maintenance of the site Quality Risk Register. Establish and drive QRM governance maturity plans to improve site performance through data-based analysis and integration of management review through site Quality Council. Function as site Risk Champion and collaborate with stakeholders to develop appropriate actions to resolve quality system issues and drive risk reduction initiatives. Facilitate risk assessment activities as required. Promote the development of a risk-aware culture at BMS and ensure alignment of these efforts with broader Quality initiatives. Support front room External Inspection activities as site SME on relevant Quality System elements. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Supporting People with Disabilities Strong working knowledge of Tech Transfer, Computer System Validation, and Commissioning and Qualification processes Strong knowledge and proven experience in applying risk management tools and methods (e.g., FMEA, PHA, HAACP, Risk Ranking and Filtering) Ability to research, understand, interpret and apply internal policies and regulatory guidelines Proficient computer skills, with knowledge of digital tools such as MS Office, and ability to learn and work with new software applications Advanced ability to interpret data & results, understand complex problems with multiple variables and critically assess and provide feedback on impact assessments and proposed actions Ability to critically review reports, interpret results, and assess and challenge technical conclusions consistent with Quality Risk Management principles Excellent verbal and technical writing skills with advanced ability to prepare written communications and present complex technical data to management with clarity and accuracy Ability to work in a fast-paced team environment and lead team and cross-functional stakeholders through changing priorities. Ability to think strategically, meet deadlines and prioritize work Ability to independently work across and influence cross-functional groups and network teams to ensure requirements are met Ability to motivate and foster a positive team environment Confident in making decisions, able to anticipate Quality issues and proactively solve problems Curious, with an ability to think critically to create innovative solutions Bachelor's degree in STEM field preferred. High school diploma/ Associates degree with equivalent combination of education and work experience may be considered. 8+ years of experience in a regulated industry, preferably with 4+ years of quality system experience including demonstrated experience with Change Control and Risk Management. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. Demonstrated proficiency with electronic system and database

About the Role/Company

  • BMS (Bristol Myers Squibb) is focused on promoting a risk-aware culture and aligning risk management efforts with broader Quality initiatives

Key Responsibilities

  • Own and maintain the Devens Cell Therapy site Change Control systems
  • Facilitate site Change Control Review Board
  • Establish and drive Change Control governance maturity plans
  • Improve site performance through data-based analysis and integration of management review
  • Support administration and maintenance of the site change control system
  • Ensure consistency with local and global change control standards and health authority regulations
  • Liaise with Technical Review Board, IT change management, and QA Technical Services teams
  • Drive technical change management solutions
  • Lead complex problem solving to deliver compliance focused solutions
  • Build & maintain strong relationships with partner functions
  • Serve as site subject matter expert on relevant quality systems
  • Own and maintain site SOPs, Work Instructions, Training documents, and business process tools
  • Own and maintain the Devens Cell Therapy site QRM systems
  • Maintain the site Quality Risk Register
  • Establish and drive QRM governance maturity plans
  • Function as site Risk Champion
  • Collaborate with stakeholders to develop actions to resolve quality system issues
  • Drive risk reduction initiatives
  • Facilitate risk assessment activities
  • Promote the development of a risk-aware culture at BMS
  • Ensure alignment of risk management efforts with broader Quality initiatives
  • Support front room External Inspection activities as site SME on relevant Quality System elements

Required Qualifications

  • Bachelor's degree in STEM field
  • High school diploma/Associates degree with equivalent combination of education and work experience
  • + years of experience in a regulated industry
  • + years of quality system experience including demonstrated experience with Change Control and Risk Management

Preferred Qualifications

  • Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing

Skills Required

  • Strong working knowledge of Tech Transfer, Computer System Validation, and Commissioning and Qualification processes
  • Strong knowledge and proven experience in applying risk management tools and methods (e.g., FMEA, PHA, HAACP, Risk Ranking and Filtering)
  • Ability to research, understand, interpret and apply internal policies and regulatory guidelines
  • Proficient computer skills, with knowledge of digital tools such as MS Office
  • Ability to learn and work with new software applications
  • Advanced ability to interpret data & results, understand complex problems with multiple variables
  • Critically assess and provide feedback on impact assessments and proposed actions
  • Ability to critically review reports, interpret results, and assess and challenge technical conclusions
  • Excellent verbal and technical writing skills
  • Advanced ability to prepare written communications and present complex technical data to management with clarity and accuracy
  • Ability to work in a fast-paced team environment and lead team and cross-functional stakeholders through changing priorities
  • Ability to think strategically, meet deadlines and prioritize work
  • Ability to independently work across and influence cross-functional groups and network teams
  • Ability to motivate and foster a positive team environment
  • Confident in making decisions, able to anticipate Quality issues and proactively solve problems
  • Curious, with an ability to think critically to create innovative solutions

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility
  • Supporting People with Disabilities

Locations

  • Devens MA, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 220,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Strong working knowledge of Tech Transfer, Computer System Validation, and Commissioning and Qualification processesintermediate
  • Strong knowledge and proven experience in applying risk management tools and methods (e.g., FMEA, PHA, HAACP, Risk Ranking and Filtering)intermediate
  • Ability to research, understand, interpret and apply internal policies and regulatory guidelinesintermediate
  • Proficient computer skills, with knowledge of digital tools such as MS Officeintermediate
  • Ability to learn and work with new software applicationsintermediate
  • Advanced ability to interpret data & results, understand complex problems with multiple variablesintermediate
  • Critically assess and provide feedback on impact assessments and proposed actionsintermediate
  • Ability to critically review reports, interpret results, and assess and challenge technical conclusionsintermediate
  • Excellent verbal and technical writing skillsintermediate
  • Advanced ability to prepare written communications and present complex technical data to management with clarity and accuracyintermediate
  • Ability to work in a fast-paced team environment and lead team and cross-functional stakeholders through changing prioritiesintermediate
  • Ability to think strategically, meet deadlines and prioritize workintermediate
  • Ability to independently work across and influence cross-functional groups and network teamsintermediate
  • Ability to motivate and foster a positive team environmentintermediate
  • Confident in making decisions, able to anticipate Quality issues and proactively solve problemsintermediate
  • Curious, with an ability to think critically to create innovative solutionsintermediate

Required Qualifications

  • Bachelor's degree in STEM field (experience)
  • High school diploma/Associates degree with equivalent combination of education and work experience (experience)
  • + years of experience in a regulated industry (experience)
  • + years of quality system experience including demonstrated experience with Change Control and Risk Management (experience)

Preferred Qualifications

  • Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing (experience)

Responsibilities

  • Own and maintain the Devens Cell Therapy site Change Control systems
  • Facilitate site Change Control Review Board
  • Establish and drive Change Control governance maturity plans
  • Improve site performance through data-based analysis and integration of management review
  • Support administration and maintenance of the site change control system
  • Ensure consistency with local and global change control standards and health authority regulations
  • Liaise with Technical Review Board, IT change management, and QA Technical Services teams
  • Drive technical change management solutions
  • Lead complex problem solving to deliver compliance focused solutions
  • Build & maintain strong relationships with partner functions
  • Serve as site subject matter expert on relevant quality systems
  • Own and maintain site SOPs, Work Instructions, Training documents, and business process tools
  • Own and maintain the Devens Cell Therapy site QRM systems
  • Maintain the site Quality Risk Register
  • Establish and drive QRM governance maturity plans
  • Function as site Risk Champion
  • Collaborate with stakeholders to develop actions to resolve quality system issues
  • Drive risk reduction initiatives
  • Facilitate risk assessment activities
  • Promote the development of a risk-aware culture at BMS
  • Ensure alignment of risk management efforts with broader Quality initiatives
  • Support front room External Inspection activities as site SME on relevant Quality System elements

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility
  • general: Supporting People with Disabilities

Target Your Resume for "Senior Manager, Quality Systems - Change Control and Quality Risk Management Process Owner" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Senior Manager, Quality Systems - Change Control and Quality Risk Management Process Owner. Takes only 15 seconds!

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

Check Your ATS Score for "Senior Manager, Quality Systems - Change Control and Quality Risk Management Process Owner" , 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.