COVID-19 is spreading fast. Do not go out unless necessary. Work from home if you can. More info at gov.uk/coronavirus
Hyper Recruitment Solutions
Back to results

QA Specialist

GlasglowPermanent
£40,000 - £45,000 per annum
Job Reference: J5634661
Updated On: 25/03/2021
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Pharmaceutical, Cell & Gene Therapy

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

Job Information

Role Overview

We are currently looking for a QA Specialist to join a leading Biopharmaceutical company based in the Central belt area. As the QA Specialist you will be responsible for ensuring Quality Assurance activities relating to product support for the manufacture, packaging, testing, storage and distribution of manufactured drug products are compliant with current GMP and company expectations.

Key Duties and Responsibilities


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

1. Managing and maintaining the vendor approval system and vendor files (both electronically and physically).

2. You will be responsible for managing suppliers performance and liaising with suppliers to complete investigations (vendor complaints) into supplier material defects. You will be responsible for maintaining and updating vendor SOPs.

3. As the QA Specialist, you will provide general support to all Quality activities relating to GMP, GCP, and other similar Quality management Systems established within the company in order to ensure that the appropriate standards and effective working systems are maintained and where necessary improved.

4. You will assist the Quality department in the overall implementation of the Quality function necessary for the maintenance of the quality management systems and related activities.

Role Requirements

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

1. Proven industry experience in a Quality assurance role within a pharmaceutical company.

2. A working knowledge and practical demonstrable experience knowledge of GMP regulations and vendor management.

Key Words: Pharmaceuticals | GMP | cGMP | Quality Assurance | Sterile | Licensed Medicines | Quality Management System | Change Control | CAPA's | Deviations | Supplier Management | Compliance | Audits | Specialist | Associate | Quality | QA | Batch Release | Documentation | KPI | Manufacturing | Specialist | Senior QA Officer | CAPAs | SOPs | Engineering | ATMP | Cell and gene therapy | supplier | vendor | manufacturing | immunotherapy | QA Specialist
Lucy Jones
Your Recruitment ConsultantLucy JonesLucy.jones@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.