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Hyper Recruitment Solutions
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QA Manager

LondonPermanent
£50,000 - £70,000 per annum
Job Reference: J5632072
Updated On: 20/08/2019
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Cell & Gene Therapy

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

Job Information

Role Overview

We are currently looking for a QA Manager to join a leading Therapeutics company based in the London area. As the QA Manager you will be responsible for managing the implementation and development of a GMP compliant Quality System.

Key Duties and Responsibilities

Your duties as the QA Manager will be varied however the key duties and responsibilities are as follows:

1. You will work cross functionally with the wider management team, participating in all GMP compliance activities, related to internal and external sites..

2. As the QA Manager, you will be tasked with the build and management of the Quality System, ensuring GMP compliance throughout. This will include developing SOP's, Monitoring Change Controls, Implementing CAPA to improve product quality, alongside reviewing Quality and Batch documentation.

3. Provide tactical support for the management of regulatory agency and client inspections, this may include acting as a site host during audits.

4. You will provide general subject expertise in Quality related issues with internal and external partners. This will include working with various regulatory agencies, including FDA & MHRA.

Role Requirements

To be successful in your application to this exciting opportunity as the QA Team Leader we are looking to identify the following on your profile and past history:

1. Relevant degree in a life sciences discipline.

2. Proven industry experience in a GMP environment producing Phase III/commercial biologic's, vaccines, cell or gene therapies.

3. A working knowledge and practical experience with EU/ MHRA FDA regulations.


Key Words: Quality Manager | Quality Assurance | QA | Manager | FDA | MHRA | ATMP | Cell Therapy | Gene Therapy | GMP | Manufacturing | Biologics | Pharma

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.