Associate Quality Assurance Manager

JR United Kingdom; Rotherham; On-site; GBP 40,000 - 70,000; Full time

Job summary

An established industry player is seeking an Associate Quality Assurance Manager to lead its QA team in Rotherham. This role is ideal for a seasoned QA professional eager to step into management while remaining hands-on in a dynamic environment. You will oversee quality assurance activities, mentor a small team, and ensure compliance with GMP standards. If you have a passion for quality and a desire to make a significant impact in a growing organization, this opportunity could be your next career move.

Qualifications

• 5+ years in pharmaceutical QA within a GMP environment.
• Experience in managing or mentoring a small team.

Responsibilities

• Lead quality assurance activities and oversee QMS.
• Coach and mentor team members in QA processes.

Skills

Quality Assurance

GMP Compliance

QMS Oversight

Auditing

Team Management

Job description

Associate Quality Assurance Manager, Rotherham

Client: RBW Consulting

Location: Rotherham, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 19

Posted: 28.04.2025

Expiry Date: 12.06.2025

Job Description:

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 yes, then this could be your next career move.

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

This is an outstanding opportunity for someone with broad quality assurance experience, spanning operational and systems activities. The team is small, offering the right candidate a chance to step into a management position.

If you enjoy coaching and mentoring and wish to formalize your management role, please apply.

For further details, please contact Mark Bux-Ryan.

Key experience:

1. Experience in a pharmaceutical QA role within a GMP environment, ideally over 5 years.
2. Experience in sterile manufacturing is advantageous but not essential.
3. Desire to manage a small team, with previous supervisory or mentoring experience.
4. Strong hands-on experience with various quality activities, especially QMS oversight.
5. Auditing experience is desirable; experience as a lead auditor is advantageous.
6. Knowledge of validation activities.

Keywords:

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