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Capa resumes in Bedminster, NJ

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Resume alert Resumes 1 - 10 of 173

Clinical Research Associate

Montville, NJ
... I created and executed CAPA to completion. Facilitate subject recruitment & participation by way of arranging Ubers to site, and other helpful extras as needed Manage and inventory site-specific IP & ancillary study supplies Proofed & edited CRFs ... - Apr 30

Quality Assurance Regulatory Affairs

Kendall Park, NJ
... • CAPA, ICH Guidelines, and Risk Management ISO 14971 • European, Japanese, Canadian, Russian, and Australian Regulatory Requirements. • Laws and regulations governing Human Research • Regulations for Orphan and Pediatric Drug Development COURSEWORK ... - Apr 29

Supply Chain Business Analyst

Frenchtown, NJ
... LIMS, Labware ELN, CTMS, CAPA, CRM/financial, ERP, SAP manufacturing, MPM, PDM, training applications/LMS systems for COTS and In-house systems and instrument qualification, validation, calibration, commissioning and decommissioning of various lab ... - Apr 09

Medical Device Project Manager

Edison, NJ
... • Requirement worked on Scientist Biochemistry, Scientist Biology, Protein Scientist, Microbiology, Research Associate, Lab analyst, Lab Technician, Project Manager, Clinical Trial Manager, Medical Director, Compliance Specialist with CAPA, ... - Apr 08

Product Development Quality Assurance

Irvington, NJ
... Compliance as per the relevant regulations Product Development ICHQ8R2, US FDA, WHO, EMA, MHRA Regulatory submission like CAPA reports, CTDs, monthly updates in inspection report response CAPA writing, Quality Risk Management, Change Control, Root ... - Apr 07

Supply Chain Clinical Trials

Monmouth Junction, NJ
... Conducted data analysis and identified trends in non-conformances for the investigative phase of CAPA (Corrective Action Preventative Action). Executed and improved metric for on time shipments (100%). Strategy included tracking sheet to monitor all ... - Mar 29

Quality Control

Dayton, NJ, 08810
... ● Document handling (i.e Change Control, Deviation, CAPA, OOS,OOT,STP, Planned Deviation, Product Complain etc..) ● Participate in Documentation Closing process after the investigation is done. ● Verify raw material and components prior to usage as ... - Mar 29

Drug Safety Information Technology

Belle Mead, NJ
... • CAPA Lead for IPOS systems, provide expertise to author QE and suggest adequate corrective/preventive measures by systematic investigation and record root cause analysis of identified problems/risk preventing recurrence. • Business member for ... - Mar 29

Business Analyst Change Management

Iselin, NJ, 07067
... Involved in supporting the CAPA implementation steps. Knowledge of QUMAS Doc Compliance, medical device quality management system (QMS) a regulatory content management for electronic control of all documentation and QUMAS Process Compliance, a ... - Mar 28

Quality Assurance Packaging Line

Colonia, NJ
... Ability to help on CAPA for finding the root cause of any incorrect incidents. SKILLS: Strong Decision making ready to meet business challenges with positive outlook. Quality Assurance floor activities. Maintaining quality assurance standard. ... - Mar 25
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