| Job alert | Jobs 51 - 60 of 70 |
Validation Specialist
Onsite Personnel LLC
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Newtown, PA
... Perform investigations as needed to support QMS Deviation/CAPA processes. Implement Corrective/Preventive Actions related QMS CAPA processes which may require validation activities. Review completed validation, PM, and calibration documentation for ... - Jun 10
Director Quality System Integration Management
Johnson & Johnson
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Titusville, NJ
... Experience working with Quality Systems is crucial (ie: Document Management, Change Control, Deviation and CAPA Management, etc.) at a process, platform, and execution level, Strong negotiation, communication, collaboration and networking skills. ... - Jun 10
Quality Assurance Manager - GMP
Clinical Dynamix
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New Jersey
... This includes documentation control, change control, deviation management, and CAPA (Corrective and Preventive Action) systems. Reviewing and Approving Documentation: Manage the document lifecycle of Standard Operating Procedures (SOPs) and ... - May 24
Contract : Deviation / Investigation Writer
Protocol Link, Inc.
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New Jersey
... • Prepare product complaint investigations • Ability to conduct in-depth interviews and gather pertinent information to drive to root cause conclusions, product impact analyses and initiations of CAPA actions, if required • Exceptional writing and ... - May 30
Manager Technical Reliability (1 of 2)
Kenvue
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Skillman, NJ
... Responsibilities will include, but not be limited to, championing proactive quality through effective CAPA deployment, approval of specific technical documents like root cause analysis and CAPA identification associated with technical commercial ... - Jun 17
Engineer, Quality
AbbVie
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Branchburg, NJ
... + Ensures investigations of plant events are completed thoroughly and documented accurately and are included in the plant CAPA system. Performs product impact analyses for plant events and places product on QA hold where appropriate. + Maintains an ... - Jun 07
Senior Manager, Packaging
Bristol Myers Squibb
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New Brunswick, NJ
... Ability to work with packaging engineering teams to provide accurate change controls and technical support for driving CAPA’s to completion. Requirements: Bachelor’s degree in science or a related field A minimum 5-7 years within Pharmaceutical ... - Jun 13
Quality Assurance Associate
Onsite Personnel LLC
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Newtown, PA
... · Review and maintain Quality Management Records (Change control, Deviation, CAPA, Root cause Investigations, Market complaints, Product recall, OOS and Outliers) to ensure compliance with procedures and assurance of due date requirements. · Review ... - Jun 10
Quality Assurance Specialist - Pharmaceuticals
Sigmapharm Laboratories
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Bensalem, PA
... and supporting · Reviewing and approving quality investigation and CAPA reports, and periodic quality trend reports; and · Providing input on all quality related matters of the company; documenting and tracking the company's regulatory commitments; ... - Jun 14
Production Manager - Diagnostic Instruments
Abbott
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Princeton, NJ
... up Establish department goals, tracking, and reporting KPIs, and drive continuous improvement efforts Ensure deviations, CAPA, change controls, process transfers, material dispositions and other business change needs are fully supported Review and ... - Jun 13