43 results for Validation Associate Jobs

Department Information Systems Job Title Computer System Validation Associate FLSA Status: Exempt Reports To Director of Information Systems and Procurement 1. Role Purpose: CSV Associate will work as help desk staff for other cross functional teams as appropriate to determine and resolve problems. ...

Company Description Validation & Engineering Group (V&EG) is a leading services supplier provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, an...

Firm Risk ManagementMorgan Stanley's Firm Risk Management (FRM) Division is an exciting and rapidly growing space. We support Morgan Stanley to achieve its business goals by partnering with business units across the Firm to realize efficient risk-adjusted returns, acting as a strategic advisor to th...

Responsible for leading validation efforts, ensuring compliance with cGMP for Nucleic Acid Solutions Division, managing validation documentation, and overseeing validation life cycle activities. Develops strategies for continuous improvement in cleaning validation, equipment qualification, and compu...

Responsible for planning, organizing, and coordinating customer validation activities, writing validation protocols and final reports, reviewing and approving validation protocols, executing validation protocols, and supporting maintenance or engineering in IQ/OQ/PQ activities. Duties include data c...

Seeking a Model Validation Senior Associate to join a growing team in the NY Metro area. This is a hybrid position that requires 3 days on site. (No sponsorship available)ResponsibilitiesAs part of the Model Risk Management team, you will be responsible for performing hands-on validations and review...

Job description Department Information Systems Job Title Computer System Validation Associate FLSA Status: Exempt Reports To Director of Information Systems and Procurement 1. Role Purpose: CSV Associate will work as help desk staff for other cross functional teams as appropriate to d...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)ResponsibilitiesParticipates...

Role: Model Validation Senior AssociateLocation: Jersey City NJ (Hybrid)Duration: Full Time EmployeeJob summary:Perform hands-on validations and reviews and write quality model validation reports; Collaborate with the Project Management Office (PMO) to maintain a viable model validation schedule, co...

Responsible for overseeing QA validation activities, ensuring compliance with GMP standards, reviewing validation protocols, leading the validation team, and collaborating with cross-functional teams for quality assurance. The role also involves supporting client audits and regulatory inspections.