Are you looking for a rewarding career in healthcare manufacturing? Join Target Healthcare Group, a pioneering pharmaceutical developer and manufacturer dedicated to innovation and saving lives.

As part of our Group, Quantum Pharmaceutical is the UK’s leading manufacturer and supplier of unlicensed medicines and hard-to-source products. With over 500 professionals across various disciplines—including pharmacists, technicians, IT, HR, procurement, warehouse, and customer service—we are one of the fastest-growing healthcare companies in the UK.

We are currently seeking a passionate Head of Operational Quality and Formulation to join our Aseptic Services team, a key part of our operations, where we manufacture life-saving chemotherapy drugs.

Why This Role Matters

This isn’t just a job—it’s an opportunity to make a real difference. You’ll be part of a team that values growth, innovation, and professional development.

Your Responsibilities

Product Release

• Overseeing processes, policies and quality teams to ensure timely and safe release of manufactured products in compliance with GMP, internal SOPs and regulatory standards.
• Act as Quality Controller on the Manufacturers Specials License for the Burnopfield manufacturing site in line with MHRA requirements.

• Establish, monitor and report on key quality related release metrics including:
  • Batch release timelines and adherence to SLA.
  • Right-First-Time (RFT) release rates.
  • Turnaround time for resolution of batch release issues.
  • Lead monthly performance reviews and contribute to site-level Quality Manager Review (QMR) forums.
  • Identify bottlenecks and lead initiatives to streamline batch documentation, review workflows and reduce release cycle time.
  • Implement and track continuous improvement projects using structured methodologies.
  • Collaborate with Production, Warehouse, training and QA to improve coordination and reduce repeat errors.

Formulation and Product Introduction

• Manage and guide new product introduction from technical feasibility to production readiness.
• Liaise with production and procurement teams to assess and control new starting materials and formulations.
• Act as a Superuser for the electronic manufacturing system to ensure formulations are developed and manufactured according to GMP, internal SOPs and regulatory standards.

Stability and Lifecycle

• Design and oversee stability programs in alignment with regulatory requirements.
• Own and monitor product lifecycle data.
• Lead root cause investigations and implement CAPAs related to formulation and product performance.
• Ensure pharmacovigilance systems are in place and monitor adherence.

Quality Systems and Compliance

• Lead deviation investigations, customer complaint assessments, risk assessments and change controls as required.
• Maintain and update SOPs, protocols and technical documentation.
• Ensure compliance with GMP, GDP and MHRA Regulations
• Support audits and contribute to PQRs, product recalls and QMS reviews.

What We’re Looking For

• GPhC registration is essential.
• Minimum 5 years' experience in pharmaceutical formulation, QA, or manufacturing. 
• Strong knowledge of GMP, GDP, and MHRA Specials guidance. 
• Excellent communication, leadership, and project coordination skills. 
• Strong data analysis and process improvement mindset. 
• Comfortable working in fast-paced, regulated, multi-site environments.
• Experience of operating in a similar role is desirable.

Why Join Us?

Career Growth - Elevate your expertise in a fast-growing, cutting-edge industry

Pension & Benefits – Including a cycle-to-work scheme

Free Food & Drinks – Enjoy complimentary refreshments at work

Vibrant Work Culture – A strong Social Committee organises regular events