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Hyper Recruitment Solutions
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QA Officer

LondonPermanent
£27,000 - £33,000 per annum
Job Reference: J5632418
Updated On: 08/11/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Medical Device, Clinical Research Organisation, Software, Technology

Skills: Quality Assurance - Permanent, Quality Assurance - GCP, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - ISO27001

Job Information

Role Overview

We are currently looking for a QA Officer to join a leading Clinical Diagnostics company based in the London area. As the QA Officer, you will be responsible for ensuring compliance across the business' operations.

Key Duties and Responsibilities

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

1. You will coordinate Quality Plans, Process Reviews and Training Reviews, to ensure best practices are implemented, whilst identifying Process Gaps and driving Continuous Improvements.

2. As the QA Officer, you will ensure continued compliance of company activities through maintaining and improving the company QMS, raising and investigating deviations through RCA, implementing effective CAPAs and Change Controls, and collating metrics and KPIs for the Quality Management Review.

3. You will support the business in preparation for Regulatory Inspections and Client Audits. You will also administer the Internal and External Audit Plans, and assist in conducting the Internal and Supplier Audits.

4. As the QA Officer, you will train staff on ISO QMS regulations and GCP standards, ensuring training is documented through maintaining the electronic Training and Document Management Systems.

Role Requirements

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

1. Experience as a Quality Professional in a regulated industry ( Pharmaceutical / Medical Device / Clinical Research ).

2. Proven industry experience in maintaining and enhancing a QMS, and coordinating audits and regulatory inspections.

3. A working knowledge and practical experience with GCP/ISO27001 regulations.


Key Words: QA / Quality Assurance / Life Sciences / Biotechnology / Medical Device / Internal Audits / External Audits / Supplier Audits / Regulatory Inspections / GCP / ICH Guidelines / Clinical Trials / Patient Data / Diagnostics / Quality Management System / Compliance

Hyper 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.
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.