|
Resume alert |
Resumes 1 - 10 of 188 |
Perth Amboy, NJ
... o Implementation, maintenance and trending nonconformance, change control and CAPA systems. o Performed routine inspections and in process Quality assurance (IPQA) test of formulations. Projects: o Formulation and evaluation of Herbal Face mist. ...
- May 22
Piscataway, NJ
... Performed GEMBA walks and lab walkthrough, created and reviewed Deviations, Change Controls, OOS, OOT, and CAPA. Actively contributed to cross-functional meetings and represented analytical functional area to team. Improved Quality Operation of the ...
- May 14
Edison, NJ
... data integrity, continuous improvement process (Agile, Scrums, DevOps & waterfall), Quality testing, Advance knowledge in GxP Regulations, Validation deliverables like SOP, CR, Val Plan, Non-CAPA & building solid reports for senior management. ...
- May 13
Levittown, PA
Vishwash Joshi * P a g e Vishwash Joshi ad5mzp@r.postjobfree.com M – +1-267-***-**** MICROBIOLOGY & QUALITY PROFESSIONAL Quality Risk Assessment & Compliance ~ Process Optimization and Validation ~ Investigation & CAPA~ Data Integrity / Reliability ...
- May 11
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
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
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
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
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
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