Veterans Tek
Commissioning, Qualification, and Validation (CQV) Engineer
Veterans Tek, Vista, California, us, 92085
About Veterans Tek
At Veterans Tek, we are committed to delivering innovative technology solutions that drive success for our clients. Our team comprises dedicated professionals who value collaboration, integrity, and excellence. We foster a culture that encourages continuous learning and growth, ensuring our employees are equipped to meet the evolving challenges of the tech industry.
Job Summary We are seeking a CQV Engineer to oversee the commissioning, qualification, and validation of systems and equipment to ensure compliance with industry standards.
Key Responsibilities
Develop and execute CQV protocols
Coordinate with project teams for system commissioning
Ensure systems meet qualification requirements
Document validation activities and results
Address any deviations and implement corrective actions
Required Skills & Qualifications
Bachelor's degree in Engineering or related field
Experience in CQV processes
Knowledge of regulatory standards (e.g., FDA, GMP)
Strong project management and documentation skills
Excellent communication and collaboration abilities
Preferred Qualifications (Nice to Have)
Experience in pharmaceutical or biotech industries
Familiarity with risk-based validation approaches
Certification in CQV methodologies
What We Offer
Competitive salary and benefits
Growth and learning opportunities
Friendly and collaborative team environment
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Job Summary We are seeking a CQV Engineer to oversee the commissioning, qualification, and validation of systems and equipment to ensure compliance with industry standards.
Key Responsibilities
Develop and execute CQV protocols
Coordinate with project teams for system commissioning
Ensure systems meet qualification requirements
Document validation activities and results
Address any deviations and implement corrective actions
Required Skills & Qualifications
Bachelor's degree in Engineering or related field
Experience in CQV processes
Knowledge of regulatory standards (e.g., FDA, GMP)
Strong project management and documentation skills
Excellent communication and collaboration abilities
Preferred Qualifications (Nice to Have)
Experience in pharmaceutical or biotech industries
Familiarity with risk-based validation approaches
Certification in CQV methodologies
What We Offer
Competitive salary and benefits
Growth and learning opportunities
Friendly and collaborative team environment
#J-18808-Ljbffr