Senior Specialist, QC Materials Management, Cell Therapy in Devens, MA
Bristol-Myers Squibb
Senior Specialist, QC Materials Management, Cell Therapy in Devens, MA
Job Description
Serve as the site representative for QC material management program and manage the lifecycle activities of QC laboratory materials. Support onboarding of new materials through document creation and change control. Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials. Implement and maintain the QC material inventory management system (e.g., Kanban). Train others on material management process and procedures as applicable. Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts. Create, revise, and review technical documents, such as SOPs and working instructions for sample management. Implement 5S and FIFO principles as appropriate. Apply critical thinking skills when working on new procedures or process improvements. Communicate effectively with management regarding task completion, roadblocks, and needs. Perform other tasks as required to support the QC laboratories. 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 Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. High problem-solving ability/mentality, technically adept and logical. Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs. Ability to work in a fast-paced team environment, meet deadlines, and prioritize work. Excellent organizational and critical thinking skills. Bachelor's degree, preferably in Chemistry, Microbiology, or related science. Advanced degree preferred. 4+ years of relevant work experience, preferably in a regulated environment. An equivalent combination of education and experience may substitute. Experience with material management and supply chain processes preferred. Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS preferred. Experience in writing and revising GMP procedures and working instructions.
Key Responsibilities
- Serve as the site representative for QC material management program
- Manage the lifecycle activities of QC laboratory materials
- Support onboarding of new materials through document creation and change control
- Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials
- Implement and maintain the QC material inventory management system (e.g., Kanban)
- Train others on material management process and procedures as applicable
- Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts
- Create, revise, and review technical documents, such as SOPs and working instructions for sample management
- Implement 5S and FIFO principles as appropriate
- Apply critical thinking skills when working on new procedures or process improvements
- Communicate effectively with management regarding task completion, roadblocks, and needs
- Perform other tasks as required to support the QC laboratories
Required Qualifications
- Bachelor's degree, preferably in Chemistry, Microbiology, or related science
- + years of relevant work experience, preferably in a regulated environment
- An equivalent combination of education and experience may substitute
- Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements
Preferred Qualifications
- Advanced degree
- Experience with material management and supply chain processes
- Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS
- Experience in writing and revising GMP procedures and working instructions
Skills Required
- High problem-solving ability/mentality
- Technically adept and logical
- Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize work
- Excellent organizational and critical thinking skills
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
Locations
- Devens MA, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
100,000 - 150,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- High problem-solving ability/mentalityintermediate
- Technically adept and logicalintermediate
- Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needsintermediate
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize workintermediate
- Excellent organizational and critical thinking skillsintermediate
Required Qualifications
- Bachelor's degree, preferably in Chemistry, Microbiology, or related science (experience)
- + years of relevant work experience, preferably in a regulated environment (experience)
- An equivalent combination of education and experience may substitute (experience)
- Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements (experience)
Preferred Qualifications
- Advanced degree (experience)
- Experience with material management and supply chain processes (experience)
- Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS (experience)
- Experience in writing and revising GMP procedures and working instructions (experience)
Responsibilities
- Serve as the site representative for QC material management program
- Manage the lifecycle activities of QC laboratory materials
- Support onboarding of new materials through document creation and change control
- Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials
- Implement and maintain the QC material inventory management system (e.g., Kanban)
- Train others on material management process and procedures as applicable
- Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts
- Create, revise, and review technical documents, such as SOPs and working instructions for sample management
- Implement 5S and FIFO principles as appropriate
- Apply critical thinking skills when working on new procedures or process improvements
- Communicate effectively with management regarding task completion, roadblocks, and needs
- Perform other tasks as required to support the QC laboratories
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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Senior Specialist, QC Materials Management, Cell Therapy in Devens, MA
Bristol-Myers Squibb
Senior Specialist, QC Materials Management, Cell Therapy in Devens, MA
Job Description
Serve as the site representative for QC material management program and manage the lifecycle activities of QC laboratory materials. Support onboarding of new materials through document creation and change control. Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials. Implement and maintain the QC material inventory management system (e.g., Kanban). Train others on material management process and procedures as applicable. Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts. Create, revise, and review technical documents, such as SOPs and working instructions for sample management. Implement 5S and FIFO principles as appropriate. Apply critical thinking skills when working on new procedures or process improvements. Communicate effectively with management regarding task completion, roadblocks, and needs. Perform other tasks as required to support the QC laboratories. 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 Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. High problem-solving ability/mentality, technically adept and logical. Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs. Ability to work in a fast-paced team environment, meet deadlines, and prioritize work. Excellent organizational and critical thinking skills. Bachelor's degree, preferably in Chemistry, Microbiology, or related science. Advanced degree preferred. 4+ years of relevant work experience, preferably in a regulated environment. An equivalent combination of education and experience may substitute. Experience with material management and supply chain processes preferred. Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS preferred. Experience in writing and revising GMP procedures and working instructions.
Key Responsibilities
- Serve as the site representative for QC material management program
- Manage the lifecycle activities of QC laboratory materials
- Support onboarding of new materials through document creation and change control
- Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials
- Implement and maintain the QC material inventory management system (e.g., Kanban)
- Train others on material management process and procedures as applicable
- Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts
- Create, revise, and review technical documents, such as SOPs and working instructions for sample management
- Implement 5S and FIFO principles as appropriate
- Apply critical thinking skills when working on new procedures or process improvements
- Communicate effectively with management regarding task completion, roadblocks, and needs
- Perform other tasks as required to support the QC laboratories
Required Qualifications
- Bachelor's degree, preferably in Chemistry, Microbiology, or related science
- + years of relevant work experience, preferably in a regulated environment
- An equivalent combination of education and experience may substitute
- Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements
Preferred Qualifications
- Advanced degree
- Experience with material management and supply chain processes
- Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS
- Experience in writing and revising GMP procedures and working instructions
Skills Required
- High problem-solving ability/mentality
- Technically adept and logical
- Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needs
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize work
- Excellent organizational and critical thinking skills
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
Locations
- Devens MA, United States
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
100,000 - 150,000 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- High problem-solving ability/mentalityintermediate
- Technically adept and logicalintermediate
- Ability to communicate effectively with peers, department management and cross-functional peers about task status, roadblocks and needsintermediate
- Ability to work in a fast-paced team environment, meet deadlines, and prioritize workintermediate
- Excellent organizational and critical thinking skillsintermediate
Required Qualifications
- Bachelor's degree, preferably in Chemistry, Microbiology, or related science (experience)
- + years of relevant work experience, preferably in a regulated environment (experience)
- An equivalent combination of education and experience may substitute (experience)
- Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements (experience)
Preferred Qualifications
- Advanced degree (experience)
- Experience with material management and supply chain processes (experience)
- Advanced knowledge of computerized systems and enterprise applications such as SAP and LIMS (experience)
- Experience in writing and revising GMP procedures and working instructions (experience)
Responsibilities
- Serve as the site representative for QC material management program
- Manage the lifecycle activities of QC laboratory materials
- Support onboarding of new materials through document creation and change control
- Collaborate with QC network functions and site functions such as QC lab, supply chain and other departments for the management of QC materials
- Implement and maintain the QC material inventory management system (e.g., Kanban)
- Train others on material management process and procedures as applicable
- Perform document revision, project, CAPA, and related tasks and/or continuous improvement efforts
- Create, revise, and review technical documents, such as SOPs and working instructions for sample management
- Implement 5S and FIFO principles as appropriate
- Apply critical thinking skills when working on new procedures or process improvements
- Communicate effectively with management regarding task completion, roadblocks, and needs
- Perform other tasks as required to support the QC laboratories
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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