Quality Assurance Officer

ROLE OVERVIEW

We're working exclusively with a Pharmaceutical Manufacturer in the Lancashire region who are offering an exciting opportunity for a Quality Assurance Officer to join them. They business are committed to delivering the highest standards of quality and safety. This full-time, on-site role offers the chance to play a vital part in maintaining compliance with strict industry regulations while supporting continuous improvement initiatives. You will work closely with cross-functional teams to uphold the integrity of pharmaceutical and biocide products, ensuring regulatory adherence and product excellence.

In this vital position, you will be responsible for implementing and maintaining quality management systems, conducting audits, and supporting regulatory inspections. Your expertise and attention to detail will directly influence the company’s reputation for quality and safety, contributing to its ongoing success and growth.

KEY DUTIES AND RESPONSIBILITIE

Your duties as the Quality Assurance Officer will be varied however the key duties and responsibilities are as follows:

Ensure ongoing compliance with GMP, ISO9001, and 14001 standards by supporting the implementation, review, and auditing of quality systems.
Assist in generating and reviewing SOPs and other quality documentation to ensure accuracy, clarity, and regulatory compliance.
Maintain and improve document control processes, including archiving and tracking quality records and metrics.
Support internal and external audits, including preparing documentation and participating in audit activities to demonstrate compliance.
As the Quality Assurance Officer, you will support management during regulatory inspections and contribute to quality improvement projects across the site.ROLE REQUIREMENTS

To be successful in your application to this exciting role as the Quality Assurance Officer we are looking to identify the following on your profile and past history:

A Degree or higher level in a scientific discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management) or equivalent job experience.
Proven understanding of GMP regulations, quality systems, and audit experience with knowledge of the MHRA Orange Guide.
A dedicated team player with excellent attention to detail, problem-solving skills, and the ability to communicate clearly across departments.WHAT’S IN IT FOR YOU?

This role offers a fantastic opportunity to develop your career within a reputable pharmaceutical company that values quality and integrity. You will be supported in your professional growth through training and exposure to various aspects of quality assurance, with the stability of a full-time, permanent position. Contributing directly to the safety of healthcare products, you’ll have a meaningful impact within a collaborative and compliant environment.

Key Words: Quality Assurance / GMP / ISO9001 / MHRA / Orange Guide / audit / regulatory compliance / SOPs / continuous improvement / pharmaceutical manufacturing / document control / quality systems

"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career