In this role you will lead QC technical projects and a team in a GMP-regulated lab. You will manage laboratory systems (LIMS/CDS), drive equipment lifecycle plans, and oversee validation and compliance programs. You’ll act as the technical lead for initiatives like new product introductions, method transfers, and system upgrades, collaborating with IT, vendors, and cross-functional teams. You will champion data integrity and continuous improvement to support audits and regulatory responses.
Responsibilities
Lead and develop a team of QC Technical Specialists with strong performance and resource planning
Manage laboratory equipment and electronic systems ensuring GMP and Data Integrity compliance
Deliver technical projects involving equipment procurement, qualification, validation, and implementation
Maintain long-term equipment replacement strategy for future needs
Lead NPI, method transfer, and compliance-related activities
Oversee change controls, deviations, and validation activities for systems and equipment
Collaborate with IT, external vendors, and cross-functional stakeholders for system effectiveness and compliance
Drive continuous improvement across QC operations and technology platforms
Support audits, inspections, regulatory submissions, and responses to technical inquiries
Champion data integrity and best practices across the laboratory environment
Key requirements
Degree in a scientific discipline or equivalent industry experience
Strong knowledge of pharmaceutical QC equipment, laboratory systems, qualification, and validation activities
Experience managing QC equipment and electronic systems in a regulated environment
Experience with LIMS and CDS
Thorough understanding of GMP regulations and Data Integrity principles
Proven ability to lead technical projects and deliver results to agreed timelines
Strong communication and stakeholder management skills
Ability to analyse complex technical information and communicate it clearly
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