Job Description

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