| Resume alert | Resumes 1 - 10 of 395 |
Quality Assurance System
Bridgewater, NJ
... Supplier Auditor Managed internal audit program: developed, executed, and then followed up with the verification of the correction effective (CAPA) to assure the internal audit-quality subsystem compliance with ISO, GMP and Affiliate requirements. ... - Jun 18
... Supplier Auditor Managed internal audit program: developed, executed, and then followed up with the verification of the correction effective (CAPA) to assure the internal audit-quality subsystem compliance with ISO, GMP and Affiliate requirements. ... - Jun 18
Production Safety and Quality Training Lead
Perth Amboy, NJ
... CMIC CMO USA Cranbury, NJ 06/2014-09/2015 Production Associate II GMP manufacturing of clinical and commercial solid dosage forms in a CMO (Contract Manufacturing Organization) for various clients. Responsible for the dispensing, mixing and ... - Jun 10
... CMIC CMO USA Cranbury, NJ 06/2014-09/2015 Production Associate II GMP manufacturing of clinical and commercial solid dosage forms in a CMO (Contract Manufacturing Organization) for various clients. Responsible for the dispensing, mixing and ... - Jun 10
Quality Control Management System
Willingboro, NJ
... · Maintaining laboratory documentation and generating reports according to company procedure and GMP requirements · Reviewing and updating test methods and procedures according to SOPs. · Have computer skills of MS Office and Laboratory Information ... - Jun 04
... · Maintaining laboratory documentation and generating reports according to company procedure and GMP requirements · Reviewing and updating test methods and procedures according to SOPs. · Have computer skills of MS Office and Laboratory Information ... - Jun 04
Business Analyst Process
Somerset, NJ, 08873
... •I was very much involved and supported business in periodic review process for all GMP applications for Site and GxP System Audit Trail Review Summary Report, FDA audit,HER. •I helped business to document functional requirement, validation process ... - May 28
... •I was very much involved and supported business in periodic review process for all GMP applications for Site and GxP System Audit Trail Review Summary Report, FDA audit,HER. •I helped business to document functional requirement, validation process ... - May 28
Clinical Research Trial
Ringoes, NJ, 08551
... OS Teamwork Cell Culture Aseptic Technique Cloning: Plasmid Digestion PCR Analysis Animal Cell Culture Bacteria Staining GMP and SOP Guidelines Flexibility Detail-Oriented Strong Dedication Organization Professional Experience: ICON PLC Clinical ... - May 21
... OS Teamwork Cell Culture Aseptic Technique Cloning: Plasmid Digestion PCR Analysis Animal Cell Culture Bacteria Staining GMP and SOP Guidelines Flexibility Detail-Oriented Strong Dedication Organization Professional Experience: ICON PLC Clinical ... - May 21
Data Entry Medical Technologist
East Windsor, NJ
... • Proficient with laboratory Standard Operating Procedures, Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP). • Ability to work cross-functionally in a team environment as well as independently as required • Manage multiple ... - May 20
... • Proficient with laboratory Standard Operating Procedures, Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP). • Ability to work cross-functionally in a team environment as well as independently as required • Manage multiple ... - May 20
Project Management Assay Development
Piscataway, NJ
... Improved quality control, lab management, and bookkeeping in accordance with the GMP. Reviewed and approved QC documents using electronic documentation systems (Veeva) Collected, sorted and processed cell samples, performed analysis, and presented ... - May 14
... Improved quality control, lab management, and bookkeeping in accordance with the GMP. Reviewed and approved QC documents using electronic documentation systems (Veeva) Collected, sorted and processed cell samples, performed analysis, and presented ... - May 14
Risk Assessment 3Rd Party
Levittown, PA
... PROFESSIONAL EXPERIENCE Technical GMP Consultant – GxP Technical Consultant on Quality and Compliance, result – oriented professional by managing multi – disciplinary team on project. Proficient at identifying deficiencies and integrating systematic ... - May 11
... PROFESSIONAL EXPERIENCE Technical GMP Consultant – GxP Technical Consultant on Quality and Compliance, result – oriented professional by managing multi – disciplinary team on project. Proficient at identifying deficiencies and integrating systematic ... - May 11
Quality Assurance Control
Piscataway, NJ
... in Mechanical Engineering SPECIAL SKILLS Quality Assurance, Quality Management, Supplier Audits, Packaging, Raw Materials, Non-conformances, New products transfer, GMP, Product Inspections IT/ AUTOMATION Excel, Word, Access, Outlook, PowerPoint, MS ... - May 10
... in Mechanical Engineering SPECIAL SKILLS Quality Assurance, Quality Management, Supplier Audits, Packaging, Raw Materials, Non-conformances, New products transfer, GMP, Product Inspections IT/ AUTOMATION Excel, Word, Access, Outlook, PowerPoint, MS ... - May 10
Project Management Senior Business
Piscataway, NJ
... are followed when using Client Health Information (PHI).Involved in assisting the QA Director, Quality Assurance to perform Quality Assurance Activities such as- Authors SOPs, Issuance, Distribution, Reviewing and controlling GMP documentation. ... - May 06
... are followed when using Client Health Information (PHI).Involved in assisting the QA Director, Quality Assurance to perform Quality Assurance Activities such as- Authors SOPs, Issuance, Distribution, Reviewing and controlling GMP documentation. ... - May 06