Job Reference: J5633834
Updated On: 14/10/2020
Status: Open to Applications
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Head of Operational Quality & QP
LondonPermanent
£100,000 per annum
Sectors: Biotechnology, MHRA QP License Holder
Skills: Quality Assurance - Permanent, Quality Assurance - GMP, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - Quality Manager, Quality Assurance - Quality Director / Head Of Quality, Quality Assurance - Biologics
Skills: Quality Assurance - Permanent, Quality Assurance - GMP, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - Quality Manager, Quality Assurance - Quality Director / Head Of Quality, Quality Assurance - Biologics
Job Information
Role Overview
We are currently looking for a Head of Operational Quality & QP to join a leading biopharmaceutical company based in the South East As the Head of Operational Quality & QP you will be responsible for developing the strategic decisions and leading the QA operations team, consisting of c. 30 people. You will also be named on the licence and be tasked with batch release duties.Key Duties and Responsibilities
Your duties as the Head of Operational Quality & QP will be varied however the key duties and responsibilities are as follows:1. You will develop and manage a team of Quality professionals, with the aim of providing a pro-active, Quality support to the businesses 24 / 7 manufacturing operations.
2. As the Head of Operational Quality & QP, you will work closely with the Quality Director to help define and implement the site Quality strategy and a Quality First culture.
3. You will have oversight of, and manage site wide Quality processes, including batch release, deviation management, CAPA management, Change Controls and Quality distribution activities.
4. You will be named on the licence as a QP and will be tasked with batch release activities.
Role Requirements
To be successful in your application to this exciting opportunity as the Head of Operational Quality & QP we are looking to identify the following on your profile and past history:1. Previous experience managing a Quality Assurance function, within a sterile manufacturing site.
2. You will be recognised as a Qualified Person. Previous release experience is essential. Release of sterile or biologic products is advantageous.
3. Experience working with regulatory agencies including MHRA and FDA.
Key Words: Quality Assurance | Head of Quality | Qualified Person | QP | Operational Quality | QMS | CAPA | Sterile | Aseptic | Bio | Management | Leadership | Senior | QA
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.
