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Validation Engineer II
Job in
Vacaville, Solano County, California, 95688, USA
Listed on 2025-12-01
Listing for:
Katalyst CRO
Full Time
position Listed on 2025-12-01
Job specializations:
-
Pharmaceutical
Quality Engineering
Job Description & How to Apply Below
Martinez, CA Salary: $90,000.00 - $ 2 months ago
Responsibilities- Perform qualification of laboratory equipment in accordance with EQ policies, plans and procedures.
- Coordinate with laboratory personnel to define qualification requirements.
- Author, review and execute equipment qualification protocols.
- Coordinate equipment qualification activities with vendors and other support groups.
- Identify business, quality, and compliance gaps.
- Sign documents for activities as authorized and described by client’s policies, procedures and job descriptions.
- Perform any other tasks as requested by Senior Management to support QC laboratory operations.
- BS/BA degree (preferably in relevant scientific discipline).
- Experience (may vary depending on site size/scope).
- Experience in the pharmaceutical, biopharmaceutical industry or an equivalent combination of education and experience.
- Knowledge of cGMP or equivalent regulations.
- Minimum of two year's experience in Validation or equipment qualification is desired.
- Ability to make sound decisions about scheduling and managing of priorities.
- Flexibility in problem solving, providing direction and work hours to meet business objectives.
- Possesses strong verbal and written communication skills and the ability to influence at all levels.
- Capable of building trustful and effective relationships.
- Able to think strategically and translate strategies into actionable plans.
- Takes responsibility, drives results, and achieves expected outcomes.
- Entry level
- Contract
- Pharmaceutical Manufacturing
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