Job Description

PM Group is currently engaged in the delivery of multiple Life Science projects in the USA. Together we will all be sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US. Outsourced Technical Services (OTS) is an integral part of our ability to support clients across the complete project life cycle. We deliver fast, flexible outsourcing solutions for clients worldwide. You will be on-site executing cutting-edge projects for Cell & Gene Therapy, Biologics, and Pharma facilities for both US and international clients.

PM Group is an employee owned, international project delivery firm with a team of 3,600+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners.

Responsibilities

• Lead and support the commissioning, qualification, and validation activities for process control systems, with a focus on DeltaV-based systems.
• Develop and execute CQV protocols, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) for DeltaV systems and associated equipment.
• Work closely with the automation and control systems teams to ensure DeltaV system integration aligns with process requirements.
• Review and validate system documentation, including Functional Requirement Specifications (FRS), Design Qualification (DQ) documents, and risk assessments.
• Perform DeltaV system testing, troubleshooting, and debugging during the commissioning and qualification phases.
• Ensure compliance with cGMP regulations, internal quality standards, and industry best practices throughout the CQV process.
• Provide training and mentorship to junior engineers and team members on DeltaV systems and CQV processes.
• Coordinate and communicate with cross-functional teams to schedule and execute commissioning and qualification tasks.
• Participate in and support internal and external audits, including preparation of required documentation and reports.
• Develop and maintain detailed reports of qualification activities, deviations, and resolution of issues.
• Support equipment and process validation efforts for new installations, expansions, and modifications in manufacturing environments.

Qualifications

• Bachelor's degree in Engineering, Process Engineering, or a related field.
• 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 a manufacturing environment.
• Strong troubleshooting and problem-solving skills.
• Excellent communication skills and the ability to collaborate with diverse teams.
• Experience with qualification and validation documentation (e.g., URS, FRS, DQ, IQ, OQ, PQ, etc.).
• Ability to work in a fast-paced environment and manage multiple priorities effectively.
• Experience in the biotech, pharmaceutical, or life sciences industries.
• DeltaV Certification or similar automation certifications.
• Knowledge of additional control systems or automation platforms is a plus.

Why PM Group?

As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy. Click to read more in our Corporate Responsibility and Heath, Safety & Well-being Report 2023.

Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future.

PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know.

RECRUITMENT AGENCIES NEED NOT APPLY

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