What are the responsibilities and job description for the CQV Engineer position at PM Group?
PM Group is a leading international project delivery firm with 3,600 employees. We specialize in delivering fast and flexible outsourcing solutions for clients worldwide.
We are currently engaged in multiple Life Science projects in the USA, working closely with clients to support their projects throughout the complete life cycle. Our teams will be executing cutting-edge projects for Cell & Gene Therapy, Biologics, and Pharma facilities for both US and international clients.
Key Responsibilities
- Lead commissioning, qualification, and validation activities for process control systems, focusing on DeltaV-based systems.
- Develop and execute CQV protocols for DeltaV systems and associated equipment, including IQ, OQ, and PQ testing.
- Work with automation and control systems teams to ensure DeltaV system integration meets process requirements.
- Review and validate system documentation, including FRS, DQ documents, and risk assessments.
- Perform DeltaV system testing, troubleshooting, and debugging during commissioning and qualification phases.
- Ensure compliance with cGMP regulations, internal quality standards, and industry best practices.
- Provide training and mentorship on DeltaV systems and CQV processes.
- Coordinate commissioning and qualification tasks with cross-functional teams.
- Participate in internal and external audits, preparing required documentation and reports.
- Develop detailed reports of qualification activities, deviations, and issue resolutions.
Requirements
- Bachelor's degree in Engineering, Process Engineering, or related field.
- At least 3 years of experience in CQV engineering, with a focus on DeltaV systems and automation platforms.
- Strong understanding of DeltaV system architecture, programming, and configuration.
- Experience with cGMP and FDA regulatory guidelines.
- Knowledge of process control, instrumentation, and automation systems in manufacturing environments.
- Strong troubleshooting and problem-solving skills.
- Excellent communication and collaboration skills.
- Experience with qualification and validation documentation.
- Ability to work in fast-paced environments and manage multiple priorities effectively.
- Experience in biotech, pharmaceutical, or life sciences industries.
- DeltaV Certification or similar automation certifications.
