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Job Details

Bristol Myers Squibb

Manager, Quality Warehouse Incoming Material


Development Manager


Devens, Massachusetts, United States

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Bristol Myers Squibb is looking for a Manager to join our Incoming and Field Quality team in Devens, MA! If you have experience in quality management of suppliers or disposition of raw materials - this is your opportunity! As a Manager for Incoming and Field Quality, you will be responsible for the Quality oversight the incoming material disposition program and provide Quality floor support for the warehouse and cryogenics facilities.

Work schedule is primarily first-shift on-site Monday through Friday. This position supports a 24/7 manufacturing facility therefore candidates may need to work a flexible schedule to support business operations.

Major Responsibilities and Duties:
  • Executes quality oversight of the incoming material process which ensures complaint receipt, inspection and release of materials used in GMP manufacturing operations.

  • Manage the disposition schedule of incoming materials through effective staffing and prioritization.

  • Oversee QA floor support of warehouse and cryogenics functional areas on a day-to-day basis, including walkthroughs and inspection readiness activities.

  • Provide guidance/support for discrepancy reporting, investigations, corrections, and actions for quality events associated with warehouse and cryogenics functional areas.

  • Reviews and approves no impact quality events / investigations.

  • Provides quality review for area documents in warehouse and cryogenics including procedures, batch records, specifications, work instructions, forms, and logbooks.

  • Supports risk management activities including planning, design and assessments associated with GMP suppliers and materials.

  • Represent quality team on cross-function meetings and improvement initiates.

  • Provides training on Quality owned procedures. May also provide guidance to less experienced staff.

Role Requirements:
  • Knowledge of science generally attained through studies resulting in a B.S., in science, engineering, biochemistry, or related discipline, or combination of education, experience and training.

  • A minimum 4 years of directly relevant experience in a regulated environment with 2 years focused on product quality is required.

  • Experience in quality management of suppliers that provide raw materials, consumables and services used in biotech bulk and finished product manufacturing is highly desirable.

  • Knowledge of US and EU cGMP regulations and guidance.

  • Working knowledge of electronic QMSs including any of the following: SAP, LIMS, TrackWise, Veeva/Infinity, SmartLAB, Syncade.

  • Work experience where attention to detail and personal accountability were critical to success.

  • Experience working in a team-based environment with a diverse group of people.

  • Excellent writing and oral communication skills are required.

  • Able to make sound decisions by exercising judgment within generally defined practices and policies and applies appropriate notification to management.


Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Physical presence at the BMS worksite or physical presence in the field is an essential job function of this role which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and enhances the Company culture.

To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application or if you are applying to a role based in the U.S. or Puerto Rico and you believe that you are unable to receive a COVID-19 vaccine due to a medical condition or sincerely held religious belief, during or any part of the recruitment process, please direct your inquiries to Visit to access our complete Equal Employment Opportunity statement.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.