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Audit Manager

Berkshire, BerkshirePermanent
£55,000 - £65,000 per annum
Job Reference: J5631403
Updated On: 02/05/2019
Status: Now Interviewing
Hyper Recruitment Solutions
Sectors: Biotechnology, MHRA QP License Holder

Skills: Quality Assurance - Permanent, Quality Assurance - GMP, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - Quality Manager, Quality Assurance - Biologics

Job Information

Role Overview

We are currently recruiting for an Audit Manager to join a global pharmaceutical company based in the London area. As the Audit Manager you will be responsible for Customer and Regulatory Audit programmes and the Investigation management processes.

Key Duties and Responsibilities

Your duties as the Audit Manager will be varied however the key duties and responsibilities are as follows:

1. You will have oversight and will conduct on-site GMP audits of customers and regulatory agencies and will identify and evaluate risks. You will also be tasked with generating and developing the audit schedule and implementing a standard Audit and Investigation process.

2. You will implement a standard Audit programme that will be used by the internal Audit team. This will be to ensure that customers receive the same standard of audits from cradle to grave. This includes the back office audit prep, the findings and investigations.

3. As the Audit Manager, you will work cross functionally to ensure that root-cause analysis is completed appropriately and that appropriate CAPA's are implemented, with the final reports being submitted efficiently.

4. You will conduct and coordinate compliance and Quality training as required. This will include generating Key Performance Indicators and audit related metrics in support of staff development.

Role Requirements

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

1. You will have previously conducted internal and external audits. Experience auditing manufacturing sites of pharmaceutical or biological products is essential.

2. Proven experience working within a Pharmaceutical company, working to strict regulatory guidelines, such as GMP and GDP standards. Knowledge of technical regulations such as GAMP 5 would be advantageous. You must have had experience hosting Regulatory Agencies, such as the MHRA or FDA.

3. People management experience is not essential for this position, however desirable.

Key Words: Quality Assurance | QA | Quality Manager | Audit | Audit Plan | Senior | GMP | GDP | Manufacturing | Pharma | EMA | MHRA | FDA | Audit Plan | CAPA | QMS | Travel
Chris Carey
Your Recruitment ConsultantChris Careychris.carey@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.