Resume and JobRESUME AND JOB
Bristol-Myers Squibb logo

Senior Specialist, Investigations, Cell Therapy in Devens, MA

Bristol-Myers Squibb

Senior Specialist, Investigations, Cell Therapy in Devens, MA

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 26, 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. At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team. The Senior Specialist, Investigations, Cell Therapy provides investigation leadership to the Devens Cell Therapy Facility. The Senior Specialist will perform root cause analysis, work with stakeholders to identify corrective and preventative actions, and facilitate impact assessments. Shifts Available: Monday - Friday, Standard Working Hours Responsibilities: Conducting and managing the resolution of root cause investigations, including impact assessments, and CAPAs as a Lead Investigator Collaborating with many different groups/organizations as a Lead Investigator including Process Engineering and Support, Engineering and Facilities, Manufacturing Operations, Quality Assurance, and Quality Control Proactively managing the progression of investigations and CAPAs to timely and compliant closure per established KPIs Presentation of investigation findings to key stakeholders and site senior management Use of Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness; Actively supporting regulatory inspections Knowledge, Skills, Abilities: Experience utilizing root cause analysis/OPEX tools and identifying corrective and preventative actions preferred Experience with Operational Excellence and Lean Manufacturing is a plus Experience in cell therapy, biologics, or vaccine manufacturing/support desired Experience in cGMP's and multi-national biopharmaceutical/cell therapy regulations desired Excellent verbal/written communication skills and ability to influence at all levels Ability to think strategically, and to translate strategy into action Ability to prioritize and provide clear direction to team members in a highly dynamic environment Minimum Requirements: Knowledge of science generally attained through studies resulting in a Bachelor's degree in science, engineering, biochemistry or related discipline plus 2-4 years' experience in biopharmaceutical operations, or its equivalent is required Working Conditions: Position may require working in Clean-Room manufacturing environment approximately 15% of the time. Remainder of work is performed in an office environment. BMSCART LI-ONSITE GPS_2025 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. Compensation Overview: Devens - MA - US: $88,190 - $106,863 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. 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. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. 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. Supporting People with Disabilities 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. Candidate Rights 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/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. 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 focused on reimagining the future of cell therapy
  • The company offers opportunities for growth and career advancement
  • BMS emphasizes a supportive culture and values of passion, innovation, urgency, accountability, inclusion, and integrity
  • The Senior Specialist, Investigations, Cell Therapy role is part of the Cell Therapy team at the Devens Cell Therapy Facility

Key Responsibilities

  • Conducting and managing the resolution of root cause investigations, including impact assessments, and CAPAs as a Lead Investigator
  • Collaborating with many different groups/organizations as a Lead Investigator including Process Engineering and Support, Engineering and Facilities, Manufacturing Operations, Quality Assurance, and Quality Control
  • Proactively managing the progression of investigations and CAPAs to timely and compliant closure per established KPIs
  • Presentation of investigation findings to key stakeholders and site senior management
  • Use of Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste
  • Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness
  • Actively supporting regulatory inspections

Required Qualifications

  • Bachelor's degree in science, engineering, biochemistry or related discipline
  • -4 years' experience in biopharmaceutical operations, or its equivalent

Preferred Qualifications

  • Experience utilizing root cause analysis/OPEX tools and identifying corrective and preventative actions
  • Experience with Operational Excellence and Lean Manufacturing
  • Experience in cell therapy, biologics, or vaccine manufacturing/support
  • Experience in cGMP's and multi-national biopharmaceutical/cell therapy regulations

Skills Required

  • Excellent verbal/written communication skills and ability to influence at all levels
  • Ability to think strategically, and to translate strategy into action
  • Ability to prioritize and provide clear direction to team members in a highly dynamic environment

Benefits & Perks

  • Competitive medical, pharmacy, dental, and vision care
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • Financial well-being resources and a 401(K)
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • Work-life programs including paid national holidays, 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
  • Parental, caregiver, bereavement, and military leave
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • Other perks like tuition reimbursement and a recognition program

Additional Requirements

  • Position may require working in Clean-Room manufacturing environment approximately 15% of the time
  • Remainder of work is performed in an office environment
  • Shifts available: Monday - Friday, Standard Working Hours
  • Site-essential roles require 100% of shifts onsite at your assigned facility

Locations

  • Devens MA, United States

Salary

88,190 - 106,863 USD / yearly

Skills Required

  • Excellent verbal/written communication skills and ability to influence at all levelsintermediate
  • Ability to think strategically, and to translate strategy into actionintermediate
  • Ability to prioritize and provide clear direction to team members in a highly dynamic environmentintermediate

Required Qualifications

  • Bachelor's degree in science, engineering, biochemistry or related discipline (experience)
  • -4 years' experience in biopharmaceutical operations, or its equivalent (experience)

Preferred Qualifications

  • Experience utilizing root cause analysis/OPEX tools and identifying corrective and preventative actions (experience)
  • Experience with Operational Excellence and Lean Manufacturing (experience)
  • Experience in cell therapy, biologics, or vaccine manufacturing/support (experience)
  • Experience in cGMP's and multi-national biopharmaceutical/cell therapy regulations (experience)

Responsibilities

  • Conducting and managing the resolution of root cause investigations, including impact assessments, and CAPAs as a Lead Investigator
  • Collaborating with many different groups/organizations as a Lead Investigator including Process Engineering and Support, Engineering and Facilities, Manufacturing Operations, Quality Assurance, and Quality Control
  • Proactively managing the progression of investigations and CAPAs to timely and compliant closure per established KPIs
  • Presentation of investigation findings to key stakeholders and site senior management
  • Use of Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste
  • Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness
  • Actively supporting regulatory inspections

Benefits

  • general: Competitive medical, pharmacy, dental, and vision care
  • general: Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • general: Financial well-being resources and a 401(K)
  • general: Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • general: Work-life programs including paid national holidays, 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
  • general: Parental, caregiver, bereavement, and military leave
  • general: Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • general: Other perks like tuition reimbursement and a recognition program

Target Your Resume for "Senior Specialist, Investigations, Cell Therapy in Devens, MA" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Senior Specialist, Investigations, Cell Therapy in Devens, MA. Takes only 15 seconds!

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

Check Your ATS Score for "Senior Specialist, Investigations, Cell Therapy in Devens, MA" , 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.

Bristol-Myers Squibb logo

Senior Specialist, Investigations, Cell Therapy in Devens, MA

Bristol-Myers Squibb

Senior Specialist, Investigations, Cell Therapy in Devens, MA

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 26, 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. At Bristol Myers Squibb we are reimagining the future of cell therapy. With our bold ambition, backed by a best-in-the-industry team and long-term commitment, we are leading the way to unlock the full promise of cell therapy as we strive to put more patients on the path to a cure. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, there's no better place than here at BMS with our Cell Therapy team. The Senior Specialist, Investigations, Cell Therapy provides investigation leadership to the Devens Cell Therapy Facility. The Senior Specialist will perform root cause analysis, work with stakeholders to identify corrective and preventative actions, and facilitate impact assessments. Shifts Available: Monday - Friday, Standard Working Hours Responsibilities: Conducting and managing the resolution of root cause investigations, including impact assessments, and CAPAs as a Lead Investigator Collaborating with many different groups/organizations as a Lead Investigator including Process Engineering and Support, Engineering and Facilities, Manufacturing Operations, Quality Assurance, and Quality Control Proactively managing the progression of investigations and CAPAs to timely and compliant closure per established KPIs Presentation of investigation findings to key stakeholders and site senior management Use of Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness; Actively supporting regulatory inspections Knowledge, Skills, Abilities: Experience utilizing root cause analysis/OPEX tools and identifying corrective and preventative actions preferred Experience with Operational Excellence and Lean Manufacturing is a plus Experience in cell therapy, biologics, or vaccine manufacturing/support desired Experience in cGMP's and multi-national biopharmaceutical/cell therapy regulations desired Excellent verbal/written communication skills and ability to influence at all levels Ability to think strategically, and to translate strategy into action Ability to prioritize and provide clear direction to team members in a highly dynamic environment Minimum Requirements: Knowledge of science generally attained through studies resulting in a Bachelor's degree in science, engineering, biochemistry or related discipline plus 2-4 years' experience in biopharmaceutical operations, or its equivalent is required Working Conditions: Position may require working in Clean-Room manufacturing environment approximately 15% of the time. Remainder of work is performed in an office environment. BMSCART LI-ONSITE GPS_2025 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. Compensation Overview: Devens - MA - US: $88,190 - $106,863 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following: Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. 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. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition program. 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. Supporting People with Disabilities 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. Candidate Rights 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/ Data Protection We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. 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 focused on reimagining the future of cell therapy
  • The company offers opportunities for growth and career advancement
  • BMS emphasizes a supportive culture and values of passion, innovation, urgency, accountability, inclusion, and integrity
  • The Senior Specialist, Investigations, Cell Therapy role is part of the Cell Therapy team at the Devens Cell Therapy Facility

Key Responsibilities

  • Conducting and managing the resolution of root cause investigations, including impact assessments, and CAPAs as a Lead Investigator
  • Collaborating with many different groups/organizations as a Lead Investigator including Process Engineering and Support, Engineering and Facilities, Manufacturing Operations, Quality Assurance, and Quality Control
  • Proactively managing the progression of investigations and CAPAs to timely and compliant closure per established KPIs
  • Presentation of investigation findings to key stakeholders and site senior management
  • Use of Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste
  • Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness
  • Actively supporting regulatory inspections

Required Qualifications

  • Bachelor's degree in science, engineering, biochemistry or related discipline
  • -4 years' experience in biopharmaceutical operations, or its equivalent

Preferred Qualifications

  • Experience utilizing root cause analysis/OPEX tools and identifying corrective and preventative actions
  • Experience with Operational Excellence and Lean Manufacturing
  • Experience in cell therapy, biologics, or vaccine manufacturing/support
  • Experience in cGMP's and multi-national biopharmaceutical/cell therapy regulations

Skills Required

  • Excellent verbal/written communication skills and ability to influence at all levels
  • Ability to think strategically, and to translate strategy into action
  • Ability to prioritize and provide clear direction to team members in a highly dynamic environment

Benefits & Perks

  • Competitive medical, pharmacy, dental, and vision care
  • Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • Financial well-being resources and a 401(K)
  • Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • Work-life programs including paid national holidays, 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
  • Parental, caregiver, bereavement, and military leave
  • Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • Other perks like tuition reimbursement and a recognition program

Additional Requirements

  • Position may require working in Clean-Room manufacturing environment approximately 15% of the time
  • Remainder of work is performed in an office environment
  • Shifts available: Monday - Friday, Standard Working Hours
  • Site-essential roles require 100% of shifts onsite at your assigned facility

Locations

  • Devens MA, United States

Salary

88,190 - 106,863 USD / yearly

Skills Required

  • Excellent verbal/written communication skills and ability to influence at all levelsintermediate
  • Ability to think strategically, and to translate strategy into actionintermediate
  • Ability to prioritize and provide clear direction to team members in a highly dynamic environmentintermediate

Required Qualifications

  • Bachelor's degree in science, engineering, biochemistry or related discipline (experience)
  • -4 years' experience in biopharmaceutical operations, or its equivalent (experience)

Preferred Qualifications

  • Experience utilizing root cause analysis/OPEX tools and identifying corrective and preventative actions (experience)
  • Experience with Operational Excellence and Lean Manufacturing (experience)
  • Experience in cell therapy, biologics, or vaccine manufacturing/support (experience)
  • Experience in cGMP's and multi-national biopharmaceutical/cell therapy regulations (experience)

Responsibilities

  • Conducting and managing the resolution of root cause investigations, including impact assessments, and CAPAs as a Lead Investigator
  • Collaborating with many different groups/organizations as a Lead Investigator including Process Engineering and Support, Engineering and Facilities, Manufacturing Operations, Quality Assurance, and Quality Control
  • Proactively managing the progression of investigations and CAPAs to timely and compliant closure per established KPIs
  • Presentation of investigation findings to key stakeholders and site senior management
  • Use of Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste
  • Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness
  • Actively supporting regulatory inspections

Benefits

  • general: Competitive medical, pharmacy, dental, and vision care
  • general: Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP)
  • general: Financial well-being resources and a 401(K)
  • general: Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection, and survivor support
  • general: Work-life programs including paid national holidays, 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
  • general: Parental, caregiver, bereavement, and military leave
  • general: Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder, and pet care resources
  • general: Other perks like tuition reimbursement and a recognition program

Target Your Resume for "Senior Specialist, Investigations, Cell Therapy in Devens, MA" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Senior Specialist, Investigations, Cell Therapy in Devens, MA. Takes only 15 seconds!

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

Check Your ATS Score for "Senior Specialist, Investigations, Cell Therapy in Devens, MA" , 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.