QC Manager

RBW Consulting; England; On-site; GBP 45,000 - 60,000; Full time

Job summary

A leading recruitment firm is seeking a QC Manager for a new facility in Manchester. You will lead a QC team and ensure timely product release while establishing laboratory protocols and equipment selection. The ideal candidate has experience in pharmaceutical GMP environments and is ready to make a significant impact in this new role.

Qualifications

• Proven experience as a QC professional within a pharmaceutical GMP capacity.
• Track record in laboratory setup, including equipment selection and SOP development.
• Hands-on approach in a smaller team environment is essential.

Responsibilities

• Manage a small QC team and laboratory for safety and timely product release.
• Oversee equipment selection, QMS implementation, and creation of SOPs.
• Influence the success of the new facility with a broad set of responsibilities.

Skills

QC professional experience in pharmaceutical GMP

HPLC

GC

People management

Validation experience

Coaching and development

Job description

QC Manager

We are delighted to be exclusively supporting a long-standing client with the launch of a new facility based in Manchester. After continued investment and expansion over the last few years, this new facility represents another milestone.

The new post QC Manager will ultimately be responsible for a small QC team and laboratory, ensuring safety and timely product release as part of an in-process manufacturing set up. However, given that this is a new set up, the initial focus will be based around set up. Therefore, the QC Manager will be instrumental in equipment selection, QMS implementation and creating SOPs.

Therefore, this is an excellent opportunity for a QC Manager that wants to take on a broad set of responsibilities that keeps them in the laboratory environment but with a real level of critical influence in the success of the site.

For further information, please contact Mark Bux-Ryan.

Key experience

• Experience QC professional within a pharmaceutical GMP capacity
• Track record and experience of broader laboratory setup ranging from equipment selection and installation, through to developing the SOPs and protocols
• Experienced within HPLC and GC would be strongly preferred
• People management experience including recruiting and selecting teams
• Validation experience is a strong advantage – both method and equipment
• The ability to remain “hands on” in a smaller team set up
• Coaching and development approach