Validation Engineer
Apply NowCompany: Crystal Equation
Location: Thousand Oaks, CA 91360
Description:
Job Description
Validation Engineer
Top 3 Must Have Skill Sets:
Responsibilities:
Requirements:
Pay range is $41 - $46 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more. Our compensation reflects the cost of labor across several US geographic markets. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.
THE PROMISES WE MAKE:
At Crystal Equation, we empower people and advance technology initiatives by building trust. Your recruiter will prep you for the interview, obtain feedback, guide you through any necessary paperwork and provide everything you need for a successful start. We will serve to empower you along the way and provide the path for your professional journey.
For more information regarding our Privacy Policy, please visit crystalequation.com/privacy.
Meet Your Recruiter
Krista McIlwaine
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Validation Engineer
Top 3 Must Have Skill Sets:
- Experience in a GMP environment, experience generating C&Q protocols, experience executing C&Q protocols
Responsibilities:
- Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines.
- Author/evaluate qualification/validation protocols including DQ, IQ, OQ, FT, PQ protocols and final reports for new or modified GMP utilities, facilities, and process equipment.
- Execute DQ, IQ, OQ, FT, PQ protocols, which involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP utilities, facilities, and process equipment.
- 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.
- Arrange and implement FAT/SAT, commissioning activities for new GMP systems in collaboration with both internal and external partners.
- Other duties may be assigned to this role.
Requirements:
- Educated to a degree level in a technical or natural scientific field.
- Demonstrable experience in a pharma organization within a C&Q/CQV corresponding role.
- Knowledge of qualification needs to cGMP guidelines.
- Familiarity with Kneat Gx Platform or other digital C&Q systems.
- Familiarity working with cross-department stakeholders.
- Knowledge of quality assurance principles.
- Experience working within project teams and various projects in parallel.
- Prior involvement working with ISPE baseline guide vol 3, vol 4 and vol 5 would be beneficial.
- Effective communication skills, both verbally and in writing.
- Able to think analytically with the ability to resolve issues.
- Able to manage own time efficiently.
- Master degree
- Bachelor degree and 2 years of experience
- Associate degree and 6 years of experience
- high school diploma / GED and 8 years of experience
Pay range is $41 - $46 per hour with full benefits available, including paid time off, medical/dental/vision/life insurance, 401K, parental leave, and more. Our compensation reflects the cost of labor across several US geographic markets. Pay is based on several factors including market location and may vary depending on job-related knowledge, skills, and experience.
THE PROMISES WE MAKE:
At Crystal Equation, we empower people and advance technology initiatives by building trust. Your recruiter will prep you for the interview, obtain feedback, guide you through any necessary paperwork and provide everything you need for a successful start. We will serve to empower you along the way and provide the path for your professional journey.
For more information regarding our Privacy Policy, please visit crystalequation.com/privacy.
Meet Your Recruiter
Krista McIlwaine
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