Senior Technical Officer

Gruopo 3D España y Portugal S.L.L.; Wrexham; On-site; GBP 42,000 - 48,000; Full time

Job summary

A leading pharmaceutical manufacturer in Wrexham seeks a Senior Technical Officer - QC Systems. The candidate will lead a team for calibration activities and ensure compliance with GMP regulations. They will have a strong technical background with experience in QC and automated systems like Empower and LabX. Supervisory experience is preferred. This role offers a salary of £42,000 - £48,000 with Monday to Friday working days.

Qualifications

• Previous experience in a pharmaceutical laboratory is essential.
• Thorough understanding of GMP, Health and Safety, and COSHH regulations.
• Strong computer skills and knowledge of QC automated systems.

Responsibilities

• Lead a team in calibration and maintenance on QC equipment.
• Manage GMP-relevant QC computerised systems.
• Support continuous improvement initiatives.

Skills

Leadership

Technical Expertise

GMP Compliance

Change Management

Troubleshooting

Education

Graduate in a relevant scientific discipline

Tools

Empower

LabX

Microsoft Office

Job description

Senior Technical Officer - QC Systems

£42,000 - £48,000

Wrexham

Days Only (Mon-Fri)

gap technical are proud to be representing one of the UK's leading pharmaceutical manufacturers in their search for a QC Systems Senior Technical Officer to work at their manufacturing site in Wrexham.

Performance Objectives

• Lead a team responsible for planning and executing scheduled calibration and maintenance activities on QC equipment.
• Provide technical expertise across QC equipment to ensure procurement, implementation, validation, and maintenance are completed in accordance with site schedules and processes.
• Troubleshoot equipment issues and coordinate with suppliers and internal QC teams to drive timely resolution.
• Oversee and manage activities relating to GMP-relevant QC computerised systems such as Empower and LabX.
• Ensure all QC systems and data are compliant with Data Integrity regulations.
• Lead equipment-related deviation investigations, generate reports, and support root cause analysis.
• Prepare and maintain GMP documentation in relation to QC operations and automated QC systems.
• Represent the QC team during internal, customer, and regulatory audits.
• Support continuous improvement initiatives to enhance the quality and efficiency of QC processes.
• Manage change control, validation of automated systems, and participate in project planning and delivery.
  
  

Person Specification

• A Graduate (or equivalent) in a relevant scientific discipline
• Previous experience within a pharmaceutical or equivalent laboratory environment is essential.
• A thorough understanding of current GMP, Health and Safety and COSHH regulations.
• Ability to lead a team that schedules and executes planned calibration/maintenance activities on QC equipment
• Strong technical knowledge of laboratory equipment and experience in instrument/equipment qualification, automated systems validation, change management and troubleshooting
• Strong computer skills and knowledge of QC pharmaceutical automated systems such as Empower and LabX, including proficient knowledge and use of Microsoft Office applications.
• Previous supervisory experience in leading a team is preferred.
• Previous experience in representing the QC group at internal, customer and regulatory audits is desirable
• Experience in project planning and delivery would be advantageous.
  
  

Apply

Please send your CV via the Apply now option on the website

If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch

This vacancy is being advertised on behalf of gap technical who are operating as an employment agency.

gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job.

Closing Date: 08/09/2025

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