Associate Quality Assurance Manager (Stoke-On-Trent)

RBW Consulting; Stoke-on-Trent; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading company in the pharmaceutical sector is seeking an Associate Quality Assurance Manager in Stoke-On-Trent. This role offers a unique opportunity for an experienced QA professional to transition into a leadership position, focusing on quality oversight in a growing team. The ideal candidate will have a strong background in GMP environments and a passion for coaching others. If you thrive in a hands-on, flat-structured environment, this could be your next career move.

Qualifications

• Over 5 years of experience in a pharmaceutical QA position within a GMP environment.
• Experience in sterile manufacturing is advantageous.
• Strong hands-on experience with quality activities, especially QMS oversight.

Responsibilities

• Step into a management role in a small quality assurance team.
• Coach and mentor team members.
• Oversee quality activities and ensure compliance with regulations.

Skills

Leadership

Coaching

Quality Assurance

Auditing

GMP

Job description

Associate Quality Assurance Manager (Stoke-On-Trent)

This is an exciting opportunity for an experienced Senior QA professional looking to step into a leadership role. If you enjoy working in a flat-structured environment where remaining hands-on is essential, this could be your next career move.

We are partnered with a business that has been supported in building its Quality team over the past 18 months. Due to increased product demand and expansion plans, they are seeking a new QA Manager for one of their UK facilities.

This role is ideal for someone with broad quality assurance experience, encompassing operational and system-focused activities. Since the team is small, there is a great opportunity for the right candidate to step into a management position. If you enjoy coaching and mentoring and are ready to take a formal management role, please apply.

For further details, please contact Mark Bux-Ryan.

Key experience:

• Experienced in a pharmaceutical QA position within a GMP environment, ideally with over 5 years of experience.
• Experience in sterile manufacturing is advantageous but not essential.
• A desire to manage a small team, supported by previous supervisory or coaching experience.
• Strong hands-on experience with a range of quality activities, especially in relation to QMS oversight.
• Auditing experience is desirable; experience as a lead auditor is advantageous.
• Knowledge and experience of validation activities.

Keywords: Quality, assurance, QA, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, compliance, regulatory, audit, lead, complaints.