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Validation Engineer Senior
Job in
Thousand Oaks, Ventura County, California, 91362, USA
Listed on 2026-06-26
Listing for:
Crystal Equation Corporation
Full Time
position Listed on 2026-06-26
Job specializations:
-
Engineering
Quality Engineering, Validation Engineer
Job Description & How to Apply Below
Validation Engineer Senior
Onsite
Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating, reviewing, and executing C&Q protocols, plans, and summary reports. Works with project teams and SMEs to develop testing strategies. Participates in project meetings to inform stakeholders on progress of C&Q activities.
Responsibilities- Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines.
- Work with project teams to develop the commissioning and qualification strategy and document it in qualification plans.
- Generate and evaluate qualification/validation protocols including IQ, OQ, FT, PQ protocols and final reports for new or modified GMP analytical and process equipment, utilities, and facilities.
- Execute IQ, OQ, FT, PQ protocols, which may involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP analytical and process equipment, utilities, and facilities.
- Ensure that Qualification/Validation plans are generated and updated for all ongoing projects.
- Prepare, evaluate and approve technical and GMP linked documentation such as URS, FMEA, impact/risk assessment, master plans, qualification/validation documentation.
- Develop and/or execute FAT/SAT and other commissioning activities for new GMP systems in collaboration with both internal and external partners.
- May include conducting validation maintenance activities including performing and scheduling periodic reviews.
- Other duties may be assigned to this role.
- Demonstrable experience in a pharmaceutical, biotech, or life science organization in a C&Q/CQV role.
- Knowledge of cGMP commissioning/qualification/validation practices.
- Familiarity with Kneat Gx Platform or other digital C&Q systems.
- Experience working with cross-functional stakeholders.
- Knowledge of quality assurance principles.
- Experience working within project teams and multiple projects in parallel.
- Effective communication skills, both verbal and written.
- Able to think analytically with the ability to resolve issues.
- Able to manage own time efficiently.
- Doctorate degree
- Masters degree and 2 years of experience
- Bachelors degree and 4 years of experience
- Associates degree and 8 years of experience
- High school diploma / GED and 10 years of experience
Position could be extended up to 3 years.
Pay range is $60 - $65 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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