CSV Analyst / Validation Analyst

Candidates need to have hands-on experience in validating and implementing infrastructure systems and tools. e.g. aws, azure, JIRA, ServiceNow etc.

Any experience with divestiture/separation a huge plus. e.g. Manufacturing site cutovers (infrastructure and applications),

• Must be able to work out of Raritan or New Brunswick Office atleast 3 days a week.
• Must be able to Independently Lead Business Separation activities for Large global & regional GxP Computerized systems. With minimal supervison.
• Recent experience with Acquisitions/Separations/Divestiture huge plus. Strong CSV Expertise, especially within Acquisition/Divestiture/Separation.
• Ability to manage end-end from Inventory, assessments, remediations to final dispositions; Infrastructure Qualifications & Business Systems Validations 7-10 years of relevant experience; has experience of leading/advising Junior and Senior resources. Specifically in the Pharmaceutical, biotechnology, or medical device industry.
• Experience in FDA and/or Global regulated environment with good understanding of GxP standards and Risk based validation; Define and implement Risk based validation activities.
• Experience in writing and executing documentation for all aspects of the validation deliverables (etc. Requirements, Compliance/validation Plans, test protocols, Test Summary reports and Compliance/Validation Reports, SOPs/WIs).
• Experience in reviewing system test and user acceptance test scripts, Traceability matrix and Design Specs Experience in QA Methodologies, designing, reviewing and approving Test Plans, systems and UAT test scripts and Test procedures. Strong verbal and written communication skills.
• Ability to work as a team player, lead a team or accomplish tasks without supervision.
• Ability to work with remote teams and support several changes/projects simultaneously. Ability to provide Validation guidance, timely reviews, and escalations to TQ management