Back to Job SearchWe are currently looking for a QC Equipment Engineer to support our client with laboratory equipment renewal, replacement, qualification and retirement in a regulated Good Manufacturing Practice (GMP) environment on an initial 6 month contract.
As the QC Equipment Engineer you will deliver defined, outcome-based work packages, helping equipment owners translate lifecycle risks into approved renewal plans, compliant documentation and completed implementation handovers. This assignment offers scope to combine technical judgement with practical delivery, keeping laboratory equipment fit for purpose and supporting business continuity. You will write SOPs for use of QC Equipment.
The QC Equipment Engineer will determine the method, sequencing and day-to-day organisation of services within agreed milestones, site-access requirements, GMP controls and health and safety obligations.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Equipment Engineer will be varied however the key duties and responsibilities are as follows:
1. As the QC Equipment Engineer you will work with equipment owners to define renewal and replacement scope, priorities, user requirements and acceptance criteria. Develop an agreed renewal plan and prioritised tracker covering equipment status, lifecycle assessments, obsolescence, criticality, dependencies, budget inputs, procurement lead times and implementation milestones.
2. As the QC Equipment Engineer you will coordinate supplier engagement, technical evaluations, quotations, purchase requisition inputs, delivery, installation, commissioning, qualification and operational handover. Monitor supplier deliverables against acceptance criteria, challenge documentation gaps and support retirement and decommissioning, including data retention, archiving, disposal and inventory updates.
3. As the QC Equipment Engineer you will prepare and coordinate inspection-ready lifecycle documentation, including risk and impact assessments, change controls, qualification plans, protocols, traceability records, reports and release-to-use records. Follow applicable standard operating procedures, current GMP, good documentation practice, data integrity expectations and approved validation and engineering standards. Support deviation and discrepancy resolution, escalating compliance, safety, delivery and business-continuity risks promptly.
4. As the QC Equipment Engineer you will coordinate focused work-package reviews, recording decisions, actions, risks and dependencies while equipment owners retain accountability for technical decisions and final approvals. Provide concise progress reporting and deliver qualification evidence, closure packs and orderly handovers of completed outputs and open actions. Complete required training and access controls, use suitable professional resources and tools and, where contractually permitted, arrange an appropriately qualified substitute subject to GMP training, confidentiality and site-access requirements.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QC Equipment Engineer we are looking to identify the following on your profile and past history:
1. Relevant degree, Higher National Certificate, Higher National Diploma or equivalent professional experience in engineering, life sciences, chemistry, biotechnology, pharmaceutical technology or a related discipline. Qualification or demonstrable training in equipment qualification, validation, project delivery or GMP quality systems would be advantageous.
2. Substantial hands-on industry experience delivering laboratory equipment renewal, replacement, qualification or lifecycle management in pharmaceutical, biotechnology or similarly regulated GMP settings. You will bring strong planning, technical writing, communication, problem-solving and stakeholder coordination skills, with the ability to work independently, exercise professional judgement and deliver against defined deadlines.
3. A working knowledge and practical experience with commissioning and qualification, risk-based validation, change control, deviations, corrective and preventive actions, data integrity and controlled documentation. Useful additional experience includes analytical instruments, controlled-temperature and laboratory support equipment, associated software, supplier assessment, factory and site acceptance testing, installation, operational and performance qualification, and asset, calibration, maintenance and validation systems. Familiarity with GAMP 5, EU GMP Annex 11, 21 CFR Part 11 and ALCOA+ principles, alongside discrete consultancy work packages, would be advantageous.
Key Words: Contract Support Specialist / Laboratory Equipment / Equipment Lifecycle Management / Equipment Renewal / GMP / Equipment Qualification / Validation / Change Control / Commissioning / Laboratory Equipment Consultant / QC Equipment Engineer
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
As the QC Equipment Engineer you will deliver defined, outcome-based work packages, helping equipment owners translate lifecycle risks into approved renewal plans, compliant documentation and completed implementation handovers. This assignment offers scope to combine technical judgement with practical delivery, keeping laboratory equipment fit for purpose and supporting business continuity. You will write SOPs for use of QC Equipment.
The QC Equipment Engineer will determine the method, sequencing and day-to-day organisation of services within agreed milestones, site-access requirements, GMP controls and health and safety obligations.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Equipment Engineer will be varied however the key duties and responsibilities are as follows:
1. As the QC Equipment Engineer you will work with equipment owners to define renewal and replacement scope, priorities, user requirements and acceptance criteria. Develop an agreed renewal plan and prioritised tracker covering equipment status, lifecycle assessments, obsolescence, criticality, dependencies, budget inputs, procurement lead times and implementation milestones.
2. As the QC Equipment Engineer you will coordinate supplier engagement, technical evaluations, quotations, purchase requisition inputs, delivery, installation, commissioning, qualification and operational handover. Monitor supplier deliverables against acceptance criteria, challenge documentation gaps and support retirement and decommissioning, including data retention, archiving, disposal and inventory updates.
3. As the QC Equipment Engineer you will prepare and coordinate inspection-ready lifecycle documentation, including risk and impact assessments, change controls, qualification plans, protocols, traceability records, reports and release-to-use records. Follow applicable standard operating procedures, current GMP, good documentation practice, data integrity expectations and approved validation and engineering standards. Support deviation and discrepancy resolution, escalating compliance, safety, delivery and business-continuity risks promptly.
4. As the QC Equipment Engineer you will coordinate focused work-package reviews, recording decisions, actions, risks and dependencies while equipment owners retain accountability for technical decisions and final approvals. Provide concise progress reporting and deliver qualification evidence, closure packs and orderly handovers of completed outputs and open actions. Complete required training and access controls, use suitable professional resources and tools and, where contractually permitted, arrange an appropriately qualified substitute subject to GMP training, confidentiality and site-access requirements.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QC Equipment Engineer we are looking to identify the following on your profile and past history:
1. Relevant degree, Higher National Certificate, Higher National Diploma or equivalent professional experience in engineering, life sciences, chemistry, biotechnology, pharmaceutical technology or a related discipline. Qualification or demonstrable training in equipment qualification, validation, project delivery or GMP quality systems would be advantageous.
2. Substantial hands-on industry experience delivering laboratory equipment renewal, replacement, qualification or lifecycle management in pharmaceutical, biotechnology or similarly regulated GMP settings. You will bring strong planning, technical writing, communication, problem-solving and stakeholder coordination skills, with the ability to work independently, exercise professional judgement and deliver against defined deadlines.
3. A working knowledge and practical experience with commissioning and qualification, risk-based validation, change control, deviations, corrective and preventive actions, data integrity and controlled documentation. Useful additional experience includes analytical instruments, controlled-temperature and laboratory support equipment, associated software, supplier assessment, factory and site acceptance testing, installation, operational and performance qualification, and asset, calibration, maintenance and validation systems. Familiarity with GAMP 5, EU GMP Annex 11, 21 CFR Part 11 and ALCOA+ principles, alongside discrete consultancy work packages, would be advantageous.
Key Words: Contract Support Specialist / Laboratory Equipment / Equipment Lifecycle Management / Equipment Renewal / GMP / Equipment Qualification / Validation / Change Control / Commissioning / Laboratory Equipment Consultant / QC Equipment Engineer
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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