- Actalent (St. Louis, MO)
- …Associate Job Description The QA Associate is responsible for the rigorous review , verification, and archival of batch records and associated documentation to ensure ... production, warehouse, and quality teams to resolve discrepancies and maintain data integrity. Responsibilities + Perform comprehensive batch record reviews for… more
- Actalent (Middletown, NY)
- …relaying physician instructions to patients. The assistant will collect patient data , manage electronic medical records, and facilitate patient care activities, ... to the patient or authorized person. + Collect patient data in person and by phone, and document patient...care provided in the electronic medical record for physician review . + Ensure accurate message taking, routing messages, and… more
- Actalent (Frederick, MD)
- …resources to maintain lab in an optimal state. * Assist with monitoring and trending data , complete routine record review of test data and related documents ... GMP systems currently in place to ensure compliance with documented policies. Review proposed changes to systems, procedures, methods, and submissions to regulatory… more
- Bristol Myers Squibb (Indianapolis, IN)
- …for operations and disposition activities at the Indianapolis facility, including review and approval of Deviations, CAPAs, Change Controls, documents, Batch ... oversight on manufacturing and validation activities. + Perform real time review of manufacturing records. + Perform periodic walkthroughs of manufacturing and… more
- Prime Therapeutics (Raleigh, NC)
- …skills. + Ability to collaborate and work well as a team. + Data review and interpretation skills required. **Preferred Qualifications** + Managed care ... Creates new and updates existing clinical algorithms based upon relevant source data (eg clinical criteria, client criteria, Medicare LCD). Provides support for… more
- WuXi AppTec (Middletown, DE)
- …audits. **Responsibilities** Microbiological Testing and Support * Perform and review advanced microbiological QC testing for drug products, raw materials, ... expertise in troubleshooting, investigations, and technical issue resolution. * Author, review , and revise SOPs, test methods, and technical documents. * Mentor… more
- Curia (Camarillo, CA)
- …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... & Environmental responsibilities. + Mentor chemists and analysts + Write, review , revise and approve: + Standard Operating Procedures (ie Laboratory Procedures)… more
- Bristol Myers Squibb (Devens, MA)
- …with regulatory and corporate guidelines. + Represent the department in product review boards, regulatory inspections (internal and external audits). Own and author ... responses to regulatory requests. + Review and approve laboratory investigations. + Champion and foster a positive and successful collaborative quality culture. +… more
- Charles River Laboratories (Mattawan, MI)
- …skills will be based on each area's training plan and business needs. + Collect, document, review , and verify data on forms, or in electronic data capture ... our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic… more
- Charles River Laboratories (Mattawan, MI)
- …skills will be based on each area's training plan and business needs. + Collect, document, review , and verify data on forms, or in electronic data capture ... our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic… more