Senior QP

RBW Consulting; Stoke-on-Trent; On-site; GBP 60,000 - 90,000; Full time

Job summary

A leading pharmaceutical manufacturer in the UK is seeking a Senior QP Manager to oversee team management and active releasing duties. Candidates should possess eligible QP status and strong experience in sterile manufacturing. The role requires flexibility and the ability to manage teams in various locations. Join a rapidly evolving company focused on growth and improvements in quality assurance.

Qualifications

• Eligible QP status in the UK.
• Strong experience in sterile manufacturing.
• Experience in coaching and developing others is beneficial.
• Willingness to travel and manage across different sites.

Responsibilities

• Split duties between active releasing and line management.
• Manage and lead a team both in person and virtually.
• Support the Head of Quality.

Skills

Eligible QP status in the UK

Strong experience of sterile manufacturing

Coaching and developing others

Flexible approach and willingness to travel

Job description

Senior QP

Due to a recent expansion in manufacturing operations, this rapidly evolving advanced pharmaceutical manufacturer is now seeking a brand new QP Manager. Having increased headcount over the past two years, especially within the Quality Assurance team, there is a need to provide additional support to the Head of Quality as the company plans for the next phase of growth.

This Lead QP will split duties between active releasing and line management of the existing team of both permanent and contract QPs. With a team of QPs based across various locations, the ability to manage and lead a team both in person and virtually, will be critical.

This business has a number of exciting challenges moving into the remainder of 2025 and beyond, including further expansion and improved systems. If you want to be a part of this next phase and have a real influence, please contact Mark Bux-Ryan or apply below.

This position can be based out operations in the West Midlands or South London.

Experience required

• Eligible QP status in the UK
• Strong experience of sterile manufacturing
• A track record of coaching and developing others is beneficial
• A flexible approach – willingness to travel at times and be present across different sites

QP, qualified, person, head, manager, lead, team, quality, QA, assurance, sterile, aseptic, terminal, sterilisation, release, batch, CAPA, investigation, complaints, MHRA, regulatory

Seniority level

• Director

Employment type

• Full-time

Job function

• Quality Assurance and Manufacturing

Industries

• Pharmaceutical Manufacturing