Staff Engineer – Process & Cleaning Validation

The Staff Engineer – Process & Cleaning Validation position is an exciting opportunity to join PM Group’s quickly growing Outsourced Technical Services(OTS) team near Zebulon, NC .

Outsourced Technical Services (OTS) is an integral part of PM Group’s ability to support clients across the complete project life cycle.

We have over 50 years’ industry experience, strong technical knowledge and integrated resources.

Clients look to us to provide experienced technical professionals that complement their project teams.

Together we are sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US.

PM Group is an employee owned, international project delivery firm with a team of 4,000+ 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.

• Lead process validation (PPQ) and cleaning validation activities.
• Develop validation strategies for new and existing products, processes, and equipment.
• Author, review, and execute validation protocols and reports.
• Analyze data and compile conclusions to support validation activities.
• Support change controls, deviation investigations, and CAPA initiatives.
• Collaborate with cross-functional teams including Manufacturing, Quality, and Technical Operations.
• Ensure compliance with cGMP requirements and regulatory expectations.
• Participate in internal and external audits and regulatory inspections.
• Drive continuous improvement initiatives related to validation programs.
• Bachelor's degree in Engineering, Chemistry, Life Sciences, or a related technical discipline.
• 8+ years of experience in process validation and/or cleaning validation within a regulated manufacturing environment.
• Hands-on experience in sterile or aseptic manufacturing environments is required.
• Strong knowledge of cleaning validation principles, including residue limits, risk assessments, and risk-based validation approaches.
• Experience with lifecycle process validation and Process Performance Qualification (PPQ).
• Strong understanding of cGMP regulations and industry standards.