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R&D Quality Administrator

Experience Dependent
Job Reference: J5634218
Updated On: 04/01/2021
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Biotechnology

Skills: Quality Assurance - GMP, Quality Assurance - Biologics, Quality Assurance - Administration, Quality Assurance - Documentation

Job Information

Role Overview

We are currently looking for a R&D Quality Administrator to join a leading Biotechnology company based in the Liverpool area. As the R&D Quality Administrator you will be responsible for

Key Duties and Responsibilities

Your duties as the R&D Quality Administrator will be varied however the key duties and responsibilities are as follows:

1. Generate and manage documents and SOPS within the QMS

2. Maintain and Implement QMS in conformance with quality policies

3. Evaluate trends and compliance levels and report any issues to senior management

4. Provide document creation support to ensure all documents are formatted to company standards and are cGMP compliant.

Role Requirements

To be successful in your application to this exciting opportunity as the R&D Quality Administrator we are looking to identify the following on your profile and past history:

1. Relevant degree in a Scientific discipline

2. Proven industry experience working with Quality management systems within a GMP environment is vital

3. A working knowledge and practical experience with various Pharmaceutical quality systems is a must.
Huseyn Hajiyev
Your Recruitment ConsultantHuseyn
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.