C&Q Engineer

Job Summary

Our client, a leading biopharmaceutical manufacturing organization, is seeking a Commissioning & Qualification (C&Q) Engineer on an initial 12-month contract to support a range of capital and operational projects within a GMP-regulated environment. This position offers the opportunity to work on equipment, utility, and facility qualification activities while contributing to the successful delivery of key site projects.

Responsibilities

• Execute commissioning, qualification, and validation activities for manufacturing equipment, utilities, and facilities
• Develop, review, and execute qualification documentation, including risk assessments, protocols, and reports
• Support installation, commissioning, and startup activities for new systems and equipment
• Perform qualification lifecycle activities in line with GMP requirements and project timelines
• Coordinate with engineering, quality, operations, and project stakeholders to ensure successful project delivery
• Support deviation investigations, change controls, and corrective actions related to qualification activitiesEnsure documentation is completed accurately and maintained in accordance with regulatory requirements
• Contribute to continuous improvement initiatives and qualification best practices across the site

Requirements

• Degree or equivalent qualification in Engineering, Life Sciences, or a related technical discipline
• Experience in a C&Q, Validation, or Engineering role within the pharmaceutical, biotechnology, or regulated manufacturing industry
• Strong knowledge of GMP requirements and qualification lifecycle activities
• Experience qualifying manufacturing equipment, utilities, facilities, or laboratory systems
• Excellent communication and stakeholder management skills
• Ability to work independently and as part of a multidisciplinary project team
• Experience working on CAPEX projects within GMP environments would be advantageous