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 t SLA.
- Right-First-Time (RFT) release rates.
- Turnarund time for resolution of batch release issues.
- Lead mnthly performance reviews and contribute to site-level Quality Manager Review (QMR) forums.
- Identify bttlenecks and lead initiatives to streamline batch documentation, review workflows and reduce release cycle time.
- Implement and track cntinuous improvement projects using structured methodologies.
- Cllaborate 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
Flexible Shifts – Between our 24-hour core operating hours, Monday – Sunday
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