Bristol-Myers Squibb Company

QA Manager - Analytical Laboratory Support

Location
New Brunswick, NJ, United States
Posted
Sep 08, 2019
Ref
R1516705
Required Education
Associate Degree
Position Type
Full time
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Summary:

• Provide Quality oversight for testing of clinical supplies (investigational products) to assure quality and compliance with Good Manufacturing Practices (GMP) and other applicable regulations and internal procedures.

• Coordinates the assignment of tasks to be performed by the assigned managers/Associates/Specialists.

• Assure the quality of manufactured products complies with all applicable regulations and guidelines.

Responsibilities:
  • Conducts, plans, schedules, or supervises the review and approval of laboratory data, and other documentation as needed.
  • Reviews and approves documents related to Quality Systems such as laboratory investigation reports (OOA, OOS), test method validation protocols or reports, test specifications, SOPs/WIs, change controls, raw material release, etc.
  • Drafts and/or reviews Quality Agreements, as requested.
  • Supports site operations during regulatory agency and third party inspections.
  • Provides on-the-job training to Quality Operations personnel and GMP training to functional areas, as appropriate.
  • Brings to the attention of the Quality Operations Management, any information relating to the impact of legislation on the functions of the department, system deviations, etc.
  • Provides reports to Management related to timely CAPA implementation, as requested.
  • Provides support to PD/DPST-Device Operations for overall quality system and review of protocols and procedures, as requested.
  • Build and foster strong relationships and partnerships with stakeholders and support groups to meet the demands of a changing business culture and environment.
  • Provides instruction and guidance on quality issues and serves as a resource for the site.
  • Adherence to BMS core behaviors


Professional experience and qualifications:
  • Knowledge of science generally attained through studies resulting in B.S. or M.S. in chemistry, pharmacy or biology or a related pharmaceutical science
  • A Ph.D. in a related science with 4-6 years of relevant experience within the pharmaceutical or healthcare industry, or a M.S. with 7-9 years experience, or a B.S. with 9-11 years experience; including 3-5+ years experience in a regulated function.
  • Knowledge of biopharmaceutical analytical methods
  • Experience within a QA/QC environment is required
  • Technical expertise in resolution of deviations and development of effective CAPA
  • Experience in Quality Management at development and/or commercial stage of pharmaceutical operations
  • Broad experience in the manufacturing of sterile and non-sterile products
  • In-depth knowledge of GMP regulations
  • Strong problem solving, interpersonal and organizational skills
  • Strong collaborative and influencing skills
  • Effective written and verbal communication
  • Computer literacy: Microsoft Office and SAP environment Trackwise┬«, PDLIMs, and other systems as required


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 the resources to pursue their goals, both at work and in their personal lives.