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Operations Associate, Cell Therapy in Devens, MA

Bristol-Myers Squibb

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Operations Associate, Cell Therapy in Devens, MA

full-timePosted: Oct 31, 2025

Job Description

Maintain a safe work environment and wear appropriate personal protective equipment (PPE) Deliver the right material, to the right location, at the right time while adhering to good manufacturing practices and standard operating procedures. The ability to recognize deviation from accepted practice is required. Perform routine Material Operations activities across the Cell Therapy Facility including cleaning and replenishment of materials, kit building, inventory cycle counting, and warehouse activities. Perform activities to directly support the manufacture of commercial and clinical Cell Therapy products: Perform SAP transactions as required and per SOP to build kits, replenish materials, cycle count inventory, and transfer material between bin locations Collaborate with cross-functional employees & department managers to solve work-related problems and perform run-the-business activities Support the event escalation and triage process as it relates to deviations & CAPAs 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. Shift is 12hr (6PM - 6AM); Panama schedule to cover 24-7-365 operations Operate in a commercial CGMP multi-product environment Job requires standing and walking within and between grade classified suites Expectation of approximately 90% of time is spent in the operations space where the work is executed Don Personal Protective Equipment (PPE) and specialized gowning as required by procedures & signage. May work with hazardous material requiring additional PPE including respiratory protection (employee must be physically capable to wear a respirator) Must be able to follow all controlled gowning requirements for entrance to suites with various grade level classifications (Grade 8 and CNC) Proficiency in MS Office applications Strong written and verbal communication skills Demonstrated experience to communicate problem statements and escalate concerns ERP experience; preferably in SAP Extended Warehouse Management (EWM) transactions Proven experience in triage of events and execution of deviations, CAPA, and other workflows in the Quality Management System (QMS); preferably in Infinity Prior experience in kitting and delivery of raw materials and consumables to Manufacturing Prior experience in handling of cold chain biological materials; prior experience with cryogenic storage (LN2) is preferred Experience with health authorities (i.e., FDA) for audit support Experience and familiarity with electronic systems including SAP, and manufacturing execution systems (MES) including Syncade and DeltaV Safety and Quality mindset; proven ability to build a culture around these values and to communicate critical information clearly and in a timely manner to team and to manager as needed Familiarity working in operational suites with various grade level classifications High school Diploma / GED. Additional post-secondary education resulting in an Associate's or Bachelor's Degree in a relevant discipline is preferred An equivalent combination of education, experience and training may substitute Preferred but not required: Certification in CPIM, CSCP, and/or CLTD Minimum 2+ years of CGMP commercial biotechnology experience; Cell Therapy experience is preferred

About the Role/Company

  • The company operates in a commercial CGMP multi-product environment
  • The company supports the manufacture of commercial and clinical Cell Therapy products

Key Responsibilities

  • Maintain a safe work environment and wear appropriate personal protective equipment (PPE)
  • Deliver the right material, to the right location, at the right time while adhering to good manufacturing practices and standard operating procedures
  • Perform routine Material Operations activities across the Cell Therapy Facility including cleaning and replenishment of materials, kit building, inventory cycle counting, and warehouse activities
  • Perform activities to directly support the manufacture of commercial and clinical Cell Therapy products
  • Perform SAP transactions as required and per SOP to build kits, replenish materials, cycle count inventory, and transfer material between bin locations
  • Collaborate with cross-functional employees & department managers to solve work-related problems and perform run-the-business activities
  • Support the event escalation and triage process as it relates to deviations & CAPAs
  • Operate in a commercial CGMP multi-product environment
  • Don Personal Protective Equipment (PPE) and specialized gowning as required by procedures & signage
  • May work with hazardous material requiring additional PPE including respiratory protection

Required Qualifications

  • High school Diploma / GED
  • Minimum 2+ years of CGMP commercial biotechnology experience

Preferred Qualifications

  • Additional post-secondary education resulting in an Associate's or Bachelor's Degree in a relevant discipline
  • Certification in CPIM, CSCP, and/or CLTD
  • Cell Therapy experience
  • Prior experience with cryogenic storage (LN2)

Skills Required

  • Proficiency in MS Office applications
  • Strong written and verbal communication skills
  • Demonstrated experience to communicate problem statements and escalate concerns
  • ERP experience; preferably in SAP Extended Warehouse Management (EWM) transactions
  • Proven experience in triage of events and execution of deviations, CAPA, and other workflows in the Quality Management System (QMS); preferably in Infinity
  • Prior experience in kitting and delivery of raw materials and consumables to Manufacturing
  • Prior experience in handling of cold chain biological materials
  • Experience with health authorities (i.e., FDA) for audit support
  • Experience and familiarity with electronic systems including SAP, and manufacturing execution systems (MES) including Syncade and DeltaV
  • Safety and Quality mindset; proven ability to build a culture around these values and to communicate critical information clearly and in a timely manner to team and to manager as needed
  • Familiarity working in operational suites with various grade level classifications

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

Additional Requirements

  • Shift is 12hr (6PM - 6AM); Panama schedule to cover 24-7-365 operations
  • Job requires standing and walking within and between grade classified suites
  • Expectation of approximately 90% of time is spent in the operations space where the work is executed
  • Must be able to follow all controlled gowning requirements for entrance to suites with various grade level classifications (Grade 8 and CNC)
  • Employee must be physically capable to wear a respirator

Locations

  • Devens MA, United States

Salary

Estimated Salary Rangemedium confidence

60,000 - 90,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Proficiency in MS Office applicationsintermediate
  • Strong written and verbal communication skillsintermediate
  • Demonstrated experience to communicate problem statements and escalate concernsintermediate
  • ERP experience; preferably in SAP Extended Warehouse Management (EWM) transactionsintermediate
  • Proven experience in triage of events and execution of deviations, CAPA, and other workflows in the Quality Management System (QMS); preferably in Infinityintermediate
  • Prior experience in kitting and delivery of raw materials and consumables to Manufacturingintermediate
  • Prior experience in handling of cold chain biological materialsintermediate
  • Experience with health authorities (i.e., FDA) for audit supportintermediate
  • Experience and familiarity with electronic systems including SAP, and manufacturing execution systems (MES) including Syncade and DeltaVintermediate
  • Safety and Quality mindset; proven ability to build a culture around these values and to communicate critical information clearly and in a timely manner to team and to manager as neededintermediate
  • Familiarity working in operational suites with various grade level classificationsintermediate

Required Qualifications

  • High school Diploma / GED (experience)
  • Minimum 2+ years of CGMP commercial biotechnology experience (experience)

Preferred Qualifications

  • Additional post-secondary education resulting in an Associate's or Bachelor's Degree in a relevant discipline (experience)
  • Certification in CPIM, CSCP, and/or CLTD (experience)
  • Cell Therapy experience (experience)
  • Prior experience with cryogenic storage (LN2) (experience)

Responsibilities

  • Maintain a safe work environment and wear appropriate personal protective equipment (PPE)
  • Deliver the right material, to the right location, at the right time while adhering to good manufacturing practices and standard operating procedures
  • Perform routine Material Operations activities across the Cell Therapy Facility including cleaning and replenishment of materials, kit building, inventory cycle counting, and warehouse activities
  • Perform activities to directly support the manufacture of commercial and clinical Cell Therapy products
  • Perform SAP transactions as required and per SOP to build kits, replenish materials, cycle count inventory, and transfer material between bin locations
  • Collaborate with cross-functional employees & department managers to solve work-related problems and perform run-the-business activities
  • Support the event escalation and triage process as it relates to deviations & CAPAs
  • Operate in a commercial CGMP multi-product environment
  • Don Personal Protective Equipment (PPE) and specialized gowning as required by procedures & signage
  • May work with hazardous material requiring additional PPE including respiratory protection

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

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Bristol-Myers Squibb logo

Operations Associate, Cell Therapy in Devens, MA

Bristol-Myers Squibb

Healthcare Jobs

Operations Associate, Cell Therapy in Devens, MA

full-timePosted: Oct 31, 2025

Job Description

Maintain a safe work environment and wear appropriate personal protective equipment (PPE) Deliver the right material, to the right location, at the right time while adhering to good manufacturing practices and standard operating procedures. The ability to recognize deviation from accepted practice is required. Perform routine Material Operations activities across the Cell Therapy Facility including cleaning and replenishment of materials, kit building, inventory cycle counting, and warehouse activities. Perform activities to directly support the manufacture of commercial and clinical Cell Therapy products: Perform SAP transactions as required and per SOP to build kits, replenish materials, cycle count inventory, and transfer material between bin locations Collaborate with cross-functional employees & department managers to solve work-related problems and perform run-the-business activities Support the event escalation and triage process as it relates to deviations & CAPAs 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. Shift is 12hr (6PM - 6AM); Panama schedule to cover 24-7-365 operations Operate in a commercial CGMP multi-product environment Job requires standing and walking within and between grade classified suites Expectation of approximately 90% of time is spent in the operations space where the work is executed Don Personal Protective Equipment (PPE) and specialized gowning as required by procedures & signage. May work with hazardous material requiring additional PPE including respiratory protection (employee must be physically capable to wear a respirator) Must be able to follow all controlled gowning requirements for entrance to suites with various grade level classifications (Grade 8 and CNC) Proficiency in MS Office applications Strong written and verbal communication skills Demonstrated experience to communicate problem statements and escalate concerns ERP experience; preferably in SAP Extended Warehouse Management (EWM) transactions Proven experience in triage of events and execution of deviations, CAPA, and other workflows in the Quality Management System (QMS); preferably in Infinity Prior experience in kitting and delivery of raw materials and consumables to Manufacturing Prior experience in handling of cold chain biological materials; prior experience with cryogenic storage (LN2) is preferred Experience with health authorities (i.e., FDA) for audit support Experience and familiarity with electronic systems including SAP, and manufacturing execution systems (MES) including Syncade and DeltaV Safety and Quality mindset; proven ability to build a culture around these values and to communicate critical information clearly and in a timely manner to team and to manager as needed Familiarity working in operational suites with various grade level classifications High school Diploma / GED. Additional post-secondary education resulting in an Associate's or Bachelor's Degree in a relevant discipline is preferred An equivalent combination of education, experience and training may substitute Preferred but not required: Certification in CPIM, CSCP, and/or CLTD Minimum 2+ years of CGMP commercial biotechnology experience; Cell Therapy experience is preferred

About the Role/Company

  • The company operates in a commercial CGMP multi-product environment
  • The company supports the manufacture of commercial and clinical Cell Therapy products

Key Responsibilities

  • Maintain a safe work environment and wear appropriate personal protective equipment (PPE)
  • Deliver the right material, to the right location, at the right time while adhering to good manufacturing practices and standard operating procedures
  • Perform routine Material Operations activities across the Cell Therapy Facility including cleaning and replenishment of materials, kit building, inventory cycle counting, and warehouse activities
  • Perform activities to directly support the manufacture of commercial and clinical Cell Therapy products
  • Perform SAP transactions as required and per SOP to build kits, replenish materials, cycle count inventory, and transfer material between bin locations
  • Collaborate with cross-functional employees & department managers to solve work-related problems and perform run-the-business activities
  • Support the event escalation and triage process as it relates to deviations & CAPAs
  • Operate in a commercial CGMP multi-product environment
  • Don Personal Protective Equipment (PPE) and specialized gowning as required by procedures & signage
  • May work with hazardous material requiring additional PPE including respiratory protection

Required Qualifications

  • High school Diploma / GED
  • Minimum 2+ years of CGMP commercial biotechnology experience

Preferred Qualifications

  • Additional post-secondary education resulting in an Associate's or Bachelor's Degree in a relevant discipline
  • Certification in CPIM, CSCP, and/or CLTD
  • Cell Therapy experience
  • Prior experience with cryogenic storage (LN2)

Skills Required

  • Proficiency in MS Office applications
  • Strong written and verbal communication skills
  • Demonstrated experience to communicate problem statements and escalate concerns
  • ERP experience; preferably in SAP Extended Warehouse Management (EWM) transactions
  • Proven experience in triage of events and execution of deviations, CAPA, and other workflows in the Quality Management System (QMS); preferably in Infinity
  • Prior experience in kitting and delivery of raw materials and consumables to Manufacturing
  • Prior experience in handling of cold chain biological materials
  • Experience with health authorities (i.e., FDA) for audit support
  • Experience and familiarity with electronic systems including SAP, and manufacturing execution systems (MES) including Syncade and DeltaV
  • Safety and Quality mindset; proven ability to build a culture around these values and to communicate critical information clearly and in a timely manner to team and to manager as needed
  • Familiarity working in operational suites with various grade level classifications

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

Additional Requirements

  • Shift is 12hr (6PM - 6AM); Panama schedule to cover 24-7-365 operations
  • Job requires standing and walking within and between grade classified suites
  • Expectation of approximately 90% of time is spent in the operations space where the work is executed
  • Must be able to follow all controlled gowning requirements for entrance to suites with various grade level classifications (Grade 8 and CNC)
  • Employee must be physically capable to wear a respirator

Locations

  • Devens MA, United States

Salary

Estimated Salary Rangemedium confidence

60,000 - 90,000 USD / yearly

Source: ai estimated

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

Skills Required

  • Proficiency in MS Office applicationsintermediate
  • Strong written and verbal communication skillsintermediate
  • Demonstrated experience to communicate problem statements and escalate concernsintermediate
  • ERP experience; preferably in SAP Extended Warehouse Management (EWM) transactionsintermediate
  • Proven experience in triage of events and execution of deviations, CAPA, and other workflows in the Quality Management System (QMS); preferably in Infinityintermediate
  • Prior experience in kitting and delivery of raw materials and consumables to Manufacturingintermediate
  • Prior experience in handling of cold chain biological materialsintermediate
  • Experience with health authorities (i.e., FDA) for audit supportintermediate
  • Experience and familiarity with electronic systems including SAP, and manufacturing execution systems (MES) including Syncade and DeltaVintermediate
  • Safety and Quality mindset; proven ability to build a culture around these values and to communicate critical information clearly and in a timely manner to team and to manager as neededintermediate
  • Familiarity working in operational suites with various grade level classificationsintermediate

Required Qualifications

  • High school Diploma / GED (experience)
  • Minimum 2+ years of CGMP commercial biotechnology experience (experience)

Preferred Qualifications

  • Additional post-secondary education resulting in an Associate's or Bachelor's Degree in a relevant discipline (experience)
  • Certification in CPIM, CSCP, and/or CLTD (experience)
  • Cell Therapy experience (experience)
  • Prior experience with cryogenic storage (LN2) (experience)

Responsibilities

  • Maintain a safe work environment and wear appropriate personal protective equipment (PPE)
  • Deliver the right material, to the right location, at the right time while adhering to good manufacturing practices and standard operating procedures
  • Perform routine Material Operations activities across the Cell Therapy Facility including cleaning and replenishment of materials, kit building, inventory cycle counting, and warehouse activities
  • Perform activities to directly support the manufacture of commercial and clinical Cell Therapy products
  • Perform SAP transactions as required and per SOP to build kits, replenish materials, cycle count inventory, and transfer material between bin locations
  • Collaborate with cross-functional employees & department managers to solve work-related problems and perform run-the-business activities
  • Support the event escalation and triage process as it relates to deviations & CAPAs
  • Operate in a commercial CGMP multi-product environment
  • Don Personal Protective Equipment (PPE) and specialized gowning as required by procedures & signage
  • May work with hazardous material requiring additional PPE including respiratory protection

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

Target Your Resume for "Operations Associate, Cell Therapy in Devens, MA" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Operations Associate, 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 "Operations Associate, 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

Answer 10 quick questions to check your fit for Operations Associate, Cell Therapy in Devens, MA @ Bristol-Myers Squibb.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.