Senior QC Technical Officer

SRG; United Kingdom; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading pharmaceutical manufacturer in North Wales is seeking a Senior QC Systems Officer. In this role, you will lead a team of QC Technicians, manage equipment qualification and ensure compliance with quality regulations. Ideal candidates will have a degree in Chemistry and proven experience in a GMP QC setting. This position offers an opportunity to play an integral part in maintaining the quality of pharmaceutical products.

Qualifications

• Degree or similar qualification in Chemistry or a relevant scientific field.
• Proven experience in a GMP Quality Control (QC) laboratory setting.
• Excellent technical knowledge relating to laboratory equipment and QC instrumentation.
• Experience in instrument qualification and troubleshooting.
• Strong computer skills and knowledge of QC Pharmaceutical Automated Systems.

Responsibilities

• Provide technical expertise and support for QC equipment and instrumentation.
• Manage the qualification and validation of new equipment.
• Ensure compliance with quality and data integrity regulations.
• Lead equipment-related deviation investigations.

Skills

Technical expertise in QC equipment

Experience in GMP QC laboratory

Knowledge of QC automated systems

Strong computer skills

Education

Degree in Chemistry or relevant field

Job description

Senior QC Systems Officer

North Wales

SRG are recruiting for a Senior QC Systems Officer to join a leading pharmaceutical manufacturer based in North Wales. This position will play an integral part in ensuring the quality of pharmaceutical products used by thousands of people on a daily basis.

In this role, you'll be a QC instrument expert and lead a team of QC Technicians to oversee the installation, validation, calibration, & maintenance of the QC equipment onsite.

The Role:

As the Senior QC Systems Officer you will lead a team to:

• Provide technical expertise & support for QC equipment & Instrumentation.
• Manage the qualification, procurement, implementation & validation of new equipment.
• Manage GMP QC computer systems, ensuring compliance with quality & data integrity regulations.
• Lead equipment related deviation investigations.

Required:

• A degree or similar qualification in Chemistry or a relevant scientific field.
• Proven experience in a GMP Quality Control (QC) laboratory setting.
• Excellent technical knowledge relating to laboratory equipment, and QC instrumentation
• Experience in Instrument & equipment qualification, change management & troubleshooting.
• Strong computer skills & knowledge of QC Pharmaceutical Automated Systems & Automated Systems Validation.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.