Qa Manager

RBW Consulting; Hempstalls; On-site; GBP 40,000 - 60,000; Full time

Job summary

An international advanced pharmaceutical and medical device business seeks a QA Manager to expand their quality and operational activities across various UK sites. The successful candidate will guide a small team and ensure effective quality assurance practices, playing a key role in implementing quality systems and leading validation efforts.

Qualifications

• Experienced in a QA capacity, working in a GMP environment.
• Leadership and management experience preferred.
• Strong hands-on experience with quality activities and QMS oversight.

Responsibilities

• Manage a small team while remaining hands-on in all areas of quality.
• Oversee systems and operational delivery and validation activities.
• Lead through coaching, mentoring, and training.

Skills

Leadership

Quality Assurance

Auditing

Validation

GMP

Job description

QA Manager

I am partnered with an international advanced pharmaceutical and medical device business that are investing seriously into expanding their quality and operational activities, especially across various sites within the UK.

After the appointment of a new senior quality leadership team, the business is now looking to bring in new management across critical sites.

Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands on in all areas of quality. This includes systems oversight, operational delivery and validation activities.

A core aspect of the role will be leadership leading a small team through hands on coaching, mentoring and training.

If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business wide, please apply below or contact Mark Bux-Ryan for further information.

Key experience:

• Experienced within a QA capacity, working in a GMP environment
• Ideally working experience of a sterile / aseptic environment working within a terminally sterile setting would be helpful these are not essential
• Leadership and management experience is preferred
• Strong hands on experience of a range of quality activities, especially in relation to QMS oversight
• Auditing experience essential if you have been a lead auditor, this would be advantageous
• Knowledge and experience of validation activities

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