CSV Lead

Job Details :

Experience in the Pharmaceutical, biotechnology, or medical device industry

3+ years' experience with System Development Lifecyle 5+ years' experience in Computer System Validation Based on the role selected

Experience in FDA and or Global regulated environment with good understanding of GxP standards and Risk based validation.

Knowledge of FDA guidance's and industry standards i.e., GAMP

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

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.

Must be able to work 3 days onsite at Raritan, NJ