What are the responsibilities and job description for the CQV Engineer position at Azzur Group?
We are seeking a CQV Engineer to support and lead qualification efforts for facilities, utilities, and equipment in a regulated manufacturing environment. The successful candidate will focus on ensuring systems are commissioned, qualified, and validated in compliance with cGMP standards and regulatory requirements.
Responsibilities:
- Lead qualification activities for cleanrooms, HVAC systems, and utilities such as purified water, compressed air, and gas systems.
- Conduct system walk-downs, verify P&IDs, and address deficiencies or deviations identified during qualification.
- Author and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols for manufacturing and laboratory equipment, including autoclaves, cryogenic freezers, and biosafety cabinets.
- Oversee validation testing to ensure compliance with regulatory standards and operational requirements.
- Prepare comprehensive qualification protocols, validation summary reports, and traceability matrices in adherence to Good Documentation Practices (GDP).
- Maintain organized and timely records to meet both internal and external audit requirements.
- Execute system testing using tools such as thermocouples, pressure sensors, and data loggers.
- Identify and resolve issues during commissioning and qualification phases.
- Work closely with project teams, including Quality Assurance, Operations, and Engineering, to ensure alignment on validation objectives.
- Support cross-functional teams during audits and regulatory inspections as a subject matter expert (SME) for CQV processes.
Qualifications
- Bachelor’s degree in Engineering, Life Sciences, or a related field.
- 3–8 years of experience in Commissioning, Qualification, and Validation (CQV) in a cGMP-regulated environment.
- Hands-on experience with facilities, utilities, and equipment qualification.
- Proficient in drafting and executing IQ/OQ/PQ protocols.
- Knowledge of regulatory guidelines such as FDA, EU GMP, and ICH.
- Familiarity with validation tools like thermocouples and data loggers.
- Strong communication and problem-solving skills.
- Health Care Plan (Medical, Dental & Vision)
- Retirement Plan (401k, IRA)
- Life Insurance (Basic, Voluntary & AD&D)
- Paid Time Off (Vacation, Sick & Public Holidays)
