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Quality Assurance Manager

Craigavon, Co. ArmaghPermanent
£60,000 per annum
Job Reference: J5633666
Updated On: 03/09/2020
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, MHRA QP License Holder

Skills: Quality Assurance - Permanent, Quality Assurance - GMP, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - Quality Manager

Job Information

Role Overview

We are currently looking for a Quality Assurance Manager to join a leading pharmaceutical manufacturing company, based in the Northern Ireland area. As the Quality Assurance Manager, you will be responsible for managing the companies Quality System (QMS), ensuring regulatory compliance with the manufacturing of pharmaceutical products.

Key Duties and Responsibilities

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

1. You will assist with the introduction, development and management of the company QMS, ensuring that operational quality requirements are adhered to, throughout site.

2. You will utilise your management experience, leading a Quality Assurance team whilst being the point of contact for Quality enquiries throughout site. You will also manage the day to day tasks and importance of the Quality Assurance team.

3. As the Quality Assurance Manager, you will identify and implement continuous improvement projects, both within the department and the wider business.

4. You will ensure the site is always updated with any changes to legislation or guidelines and other expectations of the pharmaceutical industry, focusing on GMP and quality management.

Role Requirements

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

1. Proven industry experience working within an established pharmaceutical business, managing a quality system and all of the aspects this includes. Experience managing an electronic QMS (eQMS) would be advantageous.

2. PA thorough understanding of the legal requirements and the guidance issued for the manufacturing of pharmaceutical products across Europe.

3. Previous experience managing a QA team, would be preferable.


Key Words: Quality Assurance | QA | Quality Manager | GMP | Manufacturing | CAPA | QMS | Quality Systems | Quality Lead | MHRA | FDA | eQMS | Trackwise | Q Pulse | Audit

Chris Carey
Your Recruitment ConsultantChris Careychris.carey@hyperec.com
DisclaimerHyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.