QC Lab Validation Specialist - Pharmaceutical - North West - 12 Month FTC - up to £58,000 DOE 

Job Summary

QC Lab Validation Specialist plays a pivotal role in our Quality Control (QC) team. You will ensure that laboratory equipment is correctly installed, validated, and maintained, guaranteeing compliance with GMP (Good Manufacturing Practices) and Data Integrity regulations.   You'll lead equipment qualification activities, manage documentation, train laboratory personnel, and drive continuous improvement within our laboratory systems.

Responsibilities

• Collaborate with equipment suppliers to design and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
• Develop and maintain comprehensive equipment validation documentation for GMP equipment and software, ensuring adherence to site processes.
• Create and implement equipment procedures for new installations.
• Provide comprehensive training to laboratory personnel on the operation of new equipment.
• Lead investigations and reporting for equipment-related deviations, maintaining compliance integrity.
• Drive quality and efficiency improvement initiatives within the QC department.
• Generate GMP documentation related to QC operations and laboratory automation.

Qualifications

• Bachelor's degree (Honours) or equivalent in a relevant scientific discipline.
• Demonstrated experience working within a pharmaceutical or similar regulated quality laboratory environment.
• In-depth knowledge of laboratory equipment and analytical techniques, both in theory and practice.
• Proven expertise in equipment qualification, validation, and change management procedures.
• Strong computer skills, including proficiency in QC pharmaceutical automated systems and Microsoft Office applications.
• Excellent written and verbal communication skills.
• Experience in project planning and execution.
• A thorough understanding of current GMP, Health and Safety, and COSHH regulations.