Bristol-Myers Squibb Company

QA Specialist - Drug Product (Parenteral)

Location
New Brunswick, NJ, US
Posted
Jul 12, 2018
Ref
R1507306
Required Education
Bachelors Degree
Position Type
Full time
Scope of the role
  • Support parenteral drug product manufacturing area and responsible for quality release of drug products for human use.
  • Provides quality and compliance oversight to clinical drug product manufacturing ensuring compliance with company directives and governmental regulations.
  • Provides oversite and guidance to the Product Development manufacturing with respect to current GMP regulations
  • Perform quality related functions for the site such as Quality/GMP training and support of regulatory agency inspections.


Key responsibilities
  • Perform all product release activities, which include, but are not limited to, review of batch records, analytical tests results versus specifications, and other associated GMP documentation. Ensures that disposition decisions (release or reject) are entered into the inventory management system.
  • Review and approval of all documents related to the Quality System such as investigations into quality incidents & manufacturing deviations, corrective and preventative actions, procedural documents, to ensure conformance to cGMP, BMS standards and global regulatory requirements.
  • Supports the site compliance function during regulatory agency and third party inspections.
  • Provides guidance on quality issues to the Manufacturing group.
  • Provides guidance on quality issues to the project development teams (IDTs).
  • Assist in the authoring of Quality Agreements with contract vendors and collaboration partners.
  • Escalates immediately to the supervisor, any issues impacting product quality.


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
  • Minimum of 7-9 years experience in pharmaceutical quality and/or operations at a site level, including 2-4 years experience in a regulated function
  • Experience within a QA/QC environment is an asset
  • Broad experience in the manufacturing of parenteral products
  • In-depth knowledge of cGMP regulations
  • Strong problem solving, interpersonal and organizational skills
  • Effective written and verbal communication skills
  • Computer literacy: Microsoft Office and SAP environment Trackwise┬«, PDLIMs, and other systems as required (eg DeltaV, Pilotclean)