Bristol Myers Squibb
Specialist, Label Control and Material Operations in Devens, MA
Bristol Myers Squibb, Harvard, Massachusetts, us, 01451
Specialist, Label Control and Material Operations in Devens, MA
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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 Label Control and Material Operations team is responsible for supporting site Operations activities at Devens in accordance with Bristol Myers Squibb (BMS) policies, standards, procedures, and Global current Good Manufacturing Practices (cGMPs). Functional responsibilities include performing final drug product label printing activities, ensuring accurate and timely operations to support manufacturing and supply chain activities for Cell Therapy Development and Operations (CTDO).
Shifts Available:
6 am – 6 pm, rotating schedule including holidays and weekends.
Responsibilities
Issue clinical and commercial final drug product labels
Verify the legibility and accuracy of drug product labels in accordance with approved procedures and label specifications
Ensure areas are maintained in state of compliance to always be ready for health authority inspection or audits
Perform basic troubleshooting; communicate and resolve discrepancies independently and elevate as required
Author and review department owned documents
Maintain compliance with assigned learning plan
Support integration of newer team members
Support internal and external inspections as required
Assess discrepancies for entry into quality system and initiate deviations as applicable
Participate in cross‑department and cross‑functional meetings, communicate in a professional manner and share data/knowledge within team. Build relationships with specialized functions
Knowledge, Skills, Abilities
Ability to understand, follow and apply approved procedures
Proficient computer skills with knowledge of MS Office
Ability to understand problems and propose practical solutions
Ability to communicate effectively with cross‑functional peers and various levels of cross‑functional management through written and verbal skills
Ability to work in a fast‑paced team environment with changing priorities
Detail oriented and task focused with ability to meet deadlines and prioritize assigned work
Active listening skills and ability to understand varied perspectives
Ability to independently make decisions and recognize the need for escalation of issues
Ability to seek out opportunities for improvement
Basic Requirements
Bachelor’s degree preferred. High school diploma/Associate degree with equivalent combination of education and work experience may be considered.
2+ years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
Experience with quality management systems preferred.
Experience with electronic system and databases such as Manufacturing Execution systems (MES), Enterprise Resource Planning (ERP) preferred.
Experience with labeling software and commercial label printers preferred.
Compensation Overview Devens, MA: $80,120 - $97,088
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
careers.bms.com/life-at-bms/ .
Equal Employment Opportunity Statement Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. 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 .
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
#J-18808-Ljbffr
Get AI-powered advice on this job and more exclusive features.
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 Label Control and Material Operations team is responsible for supporting site Operations activities at Devens in accordance with Bristol Myers Squibb (BMS) policies, standards, procedures, and Global current Good Manufacturing Practices (cGMPs). Functional responsibilities include performing final drug product label printing activities, ensuring accurate and timely operations to support manufacturing and supply chain activities for Cell Therapy Development and Operations (CTDO).
Shifts Available:
6 am – 6 pm, rotating schedule including holidays and weekends.
Responsibilities
Issue clinical and commercial final drug product labels
Verify the legibility and accuracy of drug product labels in accordance with approved procedures and label specifications
Ensure areas are maintained in state of compliance to always be ready for health authority inspection or audits
Perform basic troubleshooting; communicate and resolve discrepancies independently and elevate as required
Author and review department owned documents
Maintain compliance with assigned learning plan
Support integration of newer team members
Support internal and external inspections as required
Assess discrepancies for entry into quality system and initiate deviations as applicable
Participate in cross‑department and cross‑functional meetings, communicate in a professional manner and share data/knowledge within team. Build relationships with specialized functions
Knowledge, Skills, Abilities
Ability to understand, follow and apply approved procedures
Proficient computer skills with knowledge of MS Office
Ability to understand problems and propose practical solutions
Ability to communicate effectively with cross‑functional peers and various levels of cross‑functional management through written and verbal skills
Ability to work in a fast‑paced team environment with changing priorities
Detail oriented and task focused with ability to meet deadlines and prioritize assigned work
Active listening skills and ability to understand varied perspectives
Ability to independently make decisions and recognize the need for escalation of issues
Ability to seek out opportunities for improvement
Basic Requirements
Bachelor’s degree preferred. High school diploma/Associate degree with equivalent combination of education and work experience may be considered.
2+ years of relevant cGMP experience. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
Experience with quality management systems preferred.
Experience with electronic system and databases such as Manufacturing Execution systems (MES), Enterprise Resource Planning (ERP) preferred.
Experience with labeling software and commercial label printers preferred.
Compensation Overview Devens, MA: $80,120 - $97,088
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
careers.bms.com/life-at-bms/ .
Equal Employment Opportunity Statement Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. 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 .
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
#J-18808-Ljbffr