CSV Consultant
Katalyst Healthcares & Life SciencesLittle Rock, AR
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Overview
Remote
On-site
Job Description
Roles & Responsibilities:
- Ex-Pharmaceutical preferred.
- Experience in the Pharmaceutical, biotechnology, or medical device industry.
- 2+ years' experience with System Development Lifecyle.
- 3+ 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.
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FAQs About CSV Consultant Jobs at Katalyst Healthcares & Life Sciences
What is the work location for this position at Katalyst Healthcares & Life Sciences?
This job at Katalyst Healthcares & Life Sciences is located in Little Rock, AR, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Katalyst Healthcares & Life Sciences?
Employer has not shared pay details for this role.
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