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Resume alert |
Resumes 41 - 50 of 185 |
Feasterville, PA
... •Working with relevant functional areas for CAPA plans. •Defining and implementing the health authority inspection strategies in support of regulatory submissions and GCP Compliance. •Hosting Health Authority Inspections. •Authoring or reviewing QA ...
- 2023 Apr 10
Edison, NJ
... Focused on problem identification and helped in the processing of CAPA (Corrective Action & Preventive Action) reports. •Developed IQ/OQ/PQ test scripts and executed IQ/OQ protocols. •Generated Validation Summary Report to summarize and document all ...
- 2023 Apr 05
Metuchen, NJ
... Good knowledge of Quality assurance processes like sample testing, Change control, CAPA, deviations and documentation. SKILLS •Adaptability and Teamwork. •Result Driven. •Proactive approach. •Excellent Physical Stamina. •Follow Company policies cGMP ...
- 2023 Mar 02
Bridgewater, NJ
... site to capture quality related events for BMS promotional materials with the US Pharmaceutical Compliance team ● Finalized CAPA report regarding an investigation and effectively communicated a high level TRAX process to the team ● Launched a new ...
- 2023 Mar 01
Jackson, NJ
... Oversight of vendor processes for R&D and Quality CAPA management. Senior Manager, Inventory Process Excellence – Bristol-Myers Squibb Company – NJ 08/2018 – 08/2020 Directing process improvement initiatives, driving business re-engineering and ...
- 2023 Feb 24
Edison, NJ
... ● Performed effectiveness verifications on completed non-conformance / CAPA reports to ensure any implemented procedure were effective. ● Assists in the review and release of raw materials for use in the manufacturing/laboratory area ● Reviewes ...
- 2023 Jan 20
North Brunswick, NJ
... Laboratory Information Management System –(LIMS), Labware, Empower Organization Change Management Change Control, CAPA Follow up / Investigation / Closure, Deviation Process Excellence Product Quality Complain Management System Training Management ...
- 2022 Nov 11
North Brunswick, NJ
... oImplementing CAPA and Closure of the report in case of Deviations for Customer Complaints, Issues with RM/PM Vendors. oConducting GSTDs on key complaints & non-conformity. oPreparing QIR for any RM vendor, approving its document before starting ...
- 2022 Oct 25
Warren, NJ
... •Involved in CHANGE CONTROL, DEVIATIONS and laboratory INVESTIGATIONAL activities along with CAPA. •Comprehensive knowledge of ICH guidance’s cGMP, GLP and FDA regulations •Proficient in API, Finished Product Quality Control release and stability ...
- 2022 Sep 14
Heathcote, NJ
... cGxP Validation of cGMP Food-Grade & Kosher FDA CAPA documentation. Infineum: formerly ExxonMobil / Shell Chemical, Linden, NJ 3/2017 to 12/2017 Process/Project Manager/ SME / Mentor Used extensive Regulatory Compliance, Chemical, and Engineering ...
- 2022 Aug 26