Quality Assurance Specialist

£25 to £28 per hour
27 Apr 2017
25 May 2017
Georgia St John-Smith
Contract Type
Full Time
An opportunity for an experienced Quality Assurance Specialist to join a Pharmaceutical company based in the Hampshire area.

This is an exciting opportunity to be part of a fast paced environment and focus on exciting site projects. As the QA Specialist you will be involved on all elements of quality assurance with the ability to develop your skills in the QA space.


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

1. Management of changes and deviations in site data bases, support internal audits as well as external audit programme as required.

2. Routine review of master batch documents, generation of Annual Product Review data and final reports for customers and the co-ordination of customer complaint.

3. Take a lead role in on site investigation, report generation and functional CAPA's. Feedback outcome to customer as required and support the batch release process as required.

4. Provide insight and QA support, including advice to the existing team when required, with regards to the project activities to ensure compliance to regulatory standards drive the project forward.


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

1. Relevant degree in a Scientific discipline, Chemistry or Pharmaceuticals desirable.

2. Proven industry experience in Quality Assurance function in a GMP compliant Pharmaceutical company.

3. A working knowledge and practical experience with all relevant practices associated with site GMP. This includes in-depth knowledge of processing, production and packing methods for products produced at our client's site. A formal auditing qualification would be desirable.

Key Words: Quality Assurance / Quality Officer / QA Officer / GMP / Pharmaceutical QA / GMP compliance / CAPA / Validation / Process Validation / Equipment Validation / QA Specialist / Quality / Decommissioning / Decommission / Pharmaceutical / Deviation / Change Control / Compliance

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer that is happy to 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 scientists supporting science. We look forward to helping you with your next career moves.

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