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Hyper Recruitment Solutions
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QA Officer

LondonPermanent
Experience Dependant
Job Reference: J5631810
Updated On: 05/07/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Biotechnology, Medical Device, Clinical Research Organisation

Skills: Quality Assurance - Permanent, Quality Assurance - GCP, Quality Assurance - ISO13485, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - ISO9001, Quality Assurance - Clinical Supplies, 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 is maintained across the business's operations.

Key Duties and Responsibilities

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

1. As the QA Officer, you will ensure continued compliance of company activities through maintaining a QMS, providing effective training on Quality Procedures and producing quality metrics to assist the Quality Management team to track and close CAPA's.

2. You will support the business in preparation for regulatory audits, act as a record controller during customer inspections and respond to customer complaints/quality issues should they arise.

3. As the QA Officer, you will conduct internal audits, external supplier site audits, and supplier management duties.

4. You will review procedures against regulatory guidelines to ensure continued GCP compliance, they will also assist with internal audits and identify areas of continuous improvement.

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 past 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 external audits and regulatory inspections.

3. A working knowledge and practical experience with GCP / ISO13485 regulations.


Key Words: GMP / Quality Assurance / CSV / Computer Systems Validation / Systems Validation / Software Validation / GAMP5 / Pharmaceutical / GMP / GxP Infrastructure / QA / Life Sciences / Biotechnology / IT QA / Systems Validation / Software Quality Assurance / GxP Compliance / Regulatory Standards / Medical Devices / External Audits / Supplier Audits / Supplier Management / Supplier Qualification / Regulatory Inspections / Quality Risk Analysis / Validation Protocols / Validation Master Plan / 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.
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.