14474Permanent Competitive Site Based West Yorkshire, United Kingdom Updated on: 31-03-2025
ROLE OVERVIEW
We are partnered with a Global Pharmaceutical Manufacturing Organisation, based in the West Yorkshire area, to support the search for their next Head of Quality. As the Head of Quality you will play a pivotal role in site Quality Leadership, upholding cGMP requirements, and FDA/MHRA compliance needs are met.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Head of Quality will be varied however the key duties and responsibilities are as follows:
1. Manage the day-to-day activities of the Quality Assurance (QA) department to meet product release dates.
2. Identify resource requirements, coordinate approvals, and ensure the availability of necessary resources.
3. Conduct performance reviews and evaluations to facilitate competency development within the team. Ensure QA personnel are appropriately trained before carrying out their roles.
4. Work with the regulatory function to provide input on product registration needs.
5. Provide expertise and support on quality and cGMP compliance work processes. Provide batch release, incident investigation, planned deviations and management of change QA review.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Head of Quality we are looking to identify the following on your profile and past history:
1. Relevant degree in chemistry or a quality-related subject.
2. Proven industry experience leading Quality Assurance teams within the pharmaceutical sector.
3. A working knowledge and practical experience with FDA and MHRA regulatory requirements.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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