Associate Quality Assurance Manager

RBW Consulting; Rotherham; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking an Associate QA Manager to lead a small team within a dynamic and collaborative environment. This role is ideal for an experienced QA professional with a strong background in pharmaceutical quality assurance, particularly in GMP settings. The successful candidate will have the opportunity to shape the quality processes while coaching and mentoring team members. If you are passionate about quality and ready to take the next step in your career, this is an exciting opportunity to make a significant impact in a growing company.

Qualifications

• Mindestens 5 Jahre Erfahrung in der pharmazeutischen QA.
• Erfahrung in der Überwachung von QMS-Aktivitäten.

Responsibilities

• Leitung eines kleinen QA-Teams mit Fokus auf Coaching und Mentoring.
• Überwachung der Qualitätsmanagementsysteme und Validierungsaktivitäten.

Skills

Qualitätsmanagement

Auditing

Coaching und Mentoring

GMP-Umgebung

Validierungsaktivitäten

Job description

Job Description

Associate QA Manager

Are you an experienced Senior QA professional looking to step into a leadership role?

Do you enjoy working in a flat structured setting where remaining hands-on is essential?

If the answer is yes to these, then this could be your next career move.

We are partnered with a business that we have supported in building out its Quality team structure over the past 18 months. Given an increased demand on the product and further plans for the business to expand, they are now seeking a brand new QA Manager for one of their UK facilities.

This is an outstanding opportunity for someone that has established, broad, quality assurance experience across both operational and systems-focused activities. Given that the team size is only small, there is an opportunity for the right person to step into this management position.

Therefore, if you enjoy coaching and mentoring and want to make a more official step into management, please apply.

Please contact Mark Bux-Ryan for further details.

Key experience:

• Experienced within a pharmaceutical QA position, working in a GMP environment. Ideally upwards of 5 years.
• Experience of sterile manufacturing is an advantage, but not essential.
• A desire to manage a small team, ideally supported with some previous supervisory or coaching/mentoring experience.
• Strong hands-on experience of a range of quality activities, especially in relation to QMS oversight.
• Auditing experience desirable – if you have been a lead auditor, this would be advantageous.
• Knowledge and experience of validation activities.