- ManpowerGroup (Rockville, MD)
- Our client, a leader in the pharmaceutical industry, is seeking a Pharma Document Control Associate to join their team. The ideal candidate will have strong ... will align successfully in the organization. **Job Title:** Pharma Document Control Associate **Location:** Rockville, MD **Pay...per respective SOP. + Archive and maintain GLP and GMP documents with an accurate inventory, both on and… more
- Catalent Pharma Solutions (Harmans, MD)
- …are met and leading continuous improvement initiatives. The Document Control function supports both the GMP and development operations. Catalent, ... support Phase I/II/III/commercial operations. + Manages document control processes and systems for GMP activities...document control processes and systems for GMP activities in compliance with internal procedures and policies,… more
- Actalent (Hunt Valley, MD)
- …QA Associate I, Document ControlJob Description The QA Associate I, Document Control ensures compliance with cGMP and internal policies, procedures, and ... area. These may include quality operational tasks, product release, process quality, document control , quality systems or operations, or compliance. + Support… more
- ThermoFisher Scientific (Frederick, MD)
- …coat, ear plugs etc.) **Job Description** Join Thermo Fisher Scientific as a Document Control Administrator II for a meaningful career where your contributions ... 40 lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Laboratory Setting, Loud Noises (Equipment/Machinery), Some degree… more
- Catalent Pharma Solutions (Baltimore, MD)
- …Associate III Fill/Finish is responsible for supporting the overall GMP Fill/Finish manufacturing processes in accordance with Good Manufacturing Practices ... GMP ). Accountable for final formulation and filling for the...equipment for processing. + Ensure compliance with established internal control procedures. + Operate automated and semi-automated fill/finish equipment,… more
- Charles River Laboratories (Rockville, MD)
- …including investigation/deviation management, CAPA tracking, Effectiveness Verification, change control , internal and external audits. This position will facilitate ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. **Key Responsibilities and Duties:** *… more
- Catalent Pharma Solutions (Harmans, MD)
- …products from microbial and cell culture systems for Phase I/II GMP manufacturing. The **Supervisor, Central Services** performs production operations including but ... Completes daily manufacturing tasks per standard operating procedures and batch document instructions and monitors critical process parameters. + During technical… more
- Catalent Pharma Solutions (Harmans, MD)
- …recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders ... critical computer systems and laboratory documentation to support the commercial GMP manufacturing of biological drug substance and drug product. Responsibilities… more
- Catalent Pharma Solutions (Harmans, MD)
- …: + Serve as the QA-CSV liaison with the Engineering, Quality Control , IT and Validation organizations to support SaaS enterprise computer systems validation ... and LES modules, Electronic Laboratory Notebook (ELN), OpenText Documentum Electronic Document Management System (EDMS), MODA Software, JDE Edwards etc. + Design… more
- Catalent Pharma Solutions (Harmans, MD)
- …Quality Systems to implement equipment, facility, and automation change control , document revisions, and conduct equipment/system/instrumentation failure ... recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders… more