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Hyper Recruitment Solutions
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QA Associate

Greater LondonPermanent
£28,000 - £35,000 per annum
Job Reference: J5631855
Updated On: 23/09/2019
Status: Under Offer
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Biotechnology

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

Job Information

Role Overview

We are currently looking for a QA Associate to join a leading Biopharmaceutical company that offers great career development opportunities, based in the Greater London area. As the QA Associate, you will be responsible for maintaining and driving continuous improvements of the global quality compliance function. You will work closely with internal and external departments ensuring post approval compliance levels are achieved and maintained.

Key Duties and Responsibilities

Your duties as the QA Associate will be varied. However, the key duties and responsibilities are as follows:

1. You will maintain and improve existing quality processes to ensure compliant operation internally and with external vendors.

2. As the QA Associate, you will work closely with all departments to facilitate actions and maintain compliance to the CAPA, change control and complaints systems. This will involve finding the root cause through Quality Investigations and their closure in response to customer complaints

3. You will coordinate, conduct and write product quality reviews, and create and control product specifications.

4. As the QA Associate, you will perform self-inspections and follow up on internal GxP audit observations. You will also support supplier quality management processes.

Role Requirements

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

1. Hold a relevant Life Sciences degree.

2. Proven industry experience in working within QA on a manufacturing site and pharmaceutical distribution.

3. Hands on Quality Assurance experience in the Pharmaceutical/Biotech industry, with strong and current knowledge of GMDP requirements.


Key Words: Biopharmaceutical | QA | Quality Assurance | GMP | GDP | GMDP | PV | GVP | GPvP | GxP | Quality | Compliance | Suppliers | Audit | PQR | Product Quality Review | Deviation | RCA | Root Cause Analysis | CAPA | Change Control | Biotechnology | Pharmaceutical | Science

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer that is happy to 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 scientists supporting science. We look forward to helping you with your next career moves.
Rhys Evans
Your Recruitment ConsultantRhys Evansrhys.evans@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.