Job was saved successfully.
Job was removed from Saved Jobs.

Job Details


Bristol Myers Squibb

Specialist, QA Product Disposition

Equipment/Technology Specialist

Equipment and Facilities Specialist

No

Summit, New Jersey, 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.

External Job Description

Bristol-Myers Squibb is searching for a Specialist, QA Product Disposition to join our phenomenal Cell Therapy Quality team in Summit, NJ. As our Specialist, you will be responsible for quality and disposition activities in accordance with BMS policies, standards, procedures and Global cGMP. You will have also be responsible for performing incoming material release and product release.

Role Responsibilities:

  • Responsible for disposition of incoming production materials.

  • Responsible for release activities for site manufactured drug product.

  • Review executed batch documentation, labels, QC results, Environmental Monitoring reports, change controls and deviations.

  • Issue production batch records and product labels to Operations.

  • Must have ability to author and critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles.

  • Must be skilled in planning and organizing, decision-making, and building relationships.

  • Knowledge of quality processes, including material disposition, change control, product complaints, deviations, investigations, and CAPA management.

  • Able to effectively multi-task

Role Requirements:

  • B.S. degree required, minimum of two years of experience in the pharmaceutical or related industry. Equivalent combination of education and experience acceptable.

  • Must have ability to author and critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles.

  • Must have ability to assess change controls and evaluate overall impact on batch release.

  • Must have ability to author documents, SOPs, work practices and training documents.

  • Must be skilled in planning and organizing, decision-making, and building relationships.

  • Knowledge of quality processes, including material disposition, change control, product complaints, deviations, investigations, and CAPA management.

  • Able to effectively multi-task.

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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility 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.