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
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