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Hyper Recruitment Solutions
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Quality Document Control Associate

LondonPermanent
£25,000 - £35,000 per annum
Job Reference: J5632116
Updated On: 11/09/2019
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Biotechnology, Cell & Gene Therapy

Skills: Quality Assurance - Permanent, Quality Assurance - GCP, Quality Assurance - Compliance, Quality Assurance - Clinical Supplies, Quality Assurance - Archiving, Quality Assurance - Documentation, Quality Assurance - ATMPs

Job Information

Role Overview

We are currently looking for a Quality Document Control Associate to join a leading biotechnology company based in the London area. As the Quality Document Control Associate, you will be responsible for processing and maintaining documents in the Electronic Document Management System (EDMS).

Key Duties and Responsibilities

Your duties as the Quality Document Control Associate will be varied however the key duties and responsibilities are as follows:

1. Aid in EDMS management of documents and reports, applicable for GxP records within the pharmaceutical environment

2. Use Learning Management Systems (LMS) to develop training modules and qualification curriculum's

3. As the Quality Document Control Associate, You will update EDMS with new documents and records

4. Support training programmes for all EDMS users in the biotechnological surroundings

Role Requirements

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

1. Relevant degree in a life sciences related field (biology, biotechnology, pharmacology, immunology, pharmaceuticals etc)

2. Proven pharmaceutical industry experience in a GxP regulated environment, using EDMS and LMS

3. A working knowledge of biotechnology industry documentation and practical experience with Good Documentation Practises (GDP)

Key Words:

Quality Document Control Associate | QA Document Control | Quality Document Controller | QA | Quality Assurance | Quality Document Associate | Quality Document Controller | Learning Management System | LMS | GxP | GDP | Good Documentation Practices | Electronic Document Management System | CMDS | Control Document Management System | Training Matrix | Training | Training Systems | Good Pharmacovigilance Practices
Amy Darrah
Your Recruitment ConsultantAmy DarrahAmy.Darrah@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.