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Validation Engineer Senior

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Crystal Equation Corporation
Full Time position
Listed on 2026-06-26
Job specializations:
  • Engineering
    Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 60 - 65 USD Hourly USD 60.00 65.00 HOUR
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.
Requirements
  • 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.
Education
  • 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.

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Position Requirements
10+ Years work experience
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