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Quality Compliance Specialist - Auditor

£35,000 - £40,000 per annum
Job Reference: J5631467
Updated On: 24/06/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical

Skills: Quality Assurance - GMP, Quality Assurance - GDP, Quality Assurance - GLP, Quality Assurance - Auditing, Quality Assurance - ISO9001, Quality Assurance - Documentation

Job Information

Role Overview

HRS are seeking a Quality Compliance Specialist - Auditor to join a leading pharmaceutical company based in the Hertfordshire area. As the Quality Compliance Specialist you will be responsible for performing internal and external audits, and ensuring all activities meet the requirements of GMP and GLP regulations.

Key Duties and Responsibilities

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

1. Write and review Technical and Quality Agreements to ensure responsibilities are defined such that robust partnerships exist with suppliers and service providers.

2. Review and respond to customer and third-party audit and self-assessment questionnaires.

3. Perform internal audits and provide feedback to the Quality Audit Manager. Identify gaps and facilitate improvements to systems and processes to ensure adherence to current GMP guidelines.

4. Perform supplier audits and provide feedback to the Quality Audit Manager on the compliance of suppliers and service providers.

5. To ensure that all activities meet the requirements of current GMP and GLP regulations.

Role Requirements

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

1. Relevant science related degree or extensive relevant pharmaceutical experience within a GMP environment.

2. Experience in performing internal and external audits to GMP, GDP, and ISO9001 Standards, and a good understanding of EU GMP and US CFR regulations and guidelines.

3. Experience in planning and taking part in regulatory inspections.

Key Words: GMP | GLP | GDP | Audits | Auditing | Pharmaceutical | ISO9001 | Regulatory | CFR | Auditor | Quality Assurance | QA | Quality Compliance | Pharmacopoeial Standards |
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.