Senior QC Technical Officer

Career Choices Dewis Gyrfa Ltd; Isycoed; On-site; GBP 42,000 - 62,000; Full time

Job summary

SRG in North Wales is recruiting a Senior QC Systems Officer for a leading pharmaceutical manufacturer. You will lead a team of QC Technicians and oversee installation, validation, calibration and maintenance of QC equipment onsite.

You will provide technical expertise for QC instrumentation, manage qualification and validation of new equipment, and supervise GMP QC computer systems to ensure data integrity. This role requires a chemistry degree and GMP QC experience.

Qualifications

• Degree in Chemistry or a relevant scientific field is required.
• Proven experience in a GMP QC laboratory setting.
• Strong knowledge of QC instrumentation, qualification, and validation.

Responsibilities

• Lead a team of QC Technicians overseeing installation, validation, calibration and maintenance of QC equipment onsite.
• Provide technical expertise and support for QC instrumentation and systems.
• Manage qualification, procurement, implementation and validation of new equipment.
• Oversee GMP QC computer systems ensuring compliance with data integrity regulations.
• Lead investigations into equipment-related deviations.

Skills

QC instrumentation

Team leadership

GMP systems

Education

Degree in Chemistry or relevant scientific field

Tools

QC software systems

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.

Jobs are provided by the Find a Job Service from the Department for Work and Pensions (DWP).