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Hyper Recruitment Solutions
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Qualified Person

Oxfordshire, OxfordshirePermanent
Experience Dependant
Job Reference: J5631341
Updated On: 09/08/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical

Skills: Quality Assurance - Qualified Person - Permanent, Quality Assurance - GMP, Quality Assurance - GDP, Quality Assurance - GCP, Quality Assurance - Compliance, Quality Assurance - Auditing, Quality Assurance - Quality Manager, Quality Assurance - Clinical Supplies, Quality Assurance - Biologics

Job Information

Role Overview

We are currently looking for a Qualified Person (QP) to join a leading Science business based in the Oxfordshire region. As the Qualified Person (QP) you will be responsible for the day to day batch release activities whilst ensuring GMP and GDP compliance on site.

Key Duties and Responsibilities

Your duties as the Qualified Person (QP) will be varied however the key duties and responsibilities are as following:

1. You will ensure that all batches are manufactured in accordance with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP). You will also ensure that batches and it's manufacture comply with the provisions of the marketing authorisation.

2. As the Qualified Person (QP) you will verify that all audits have been carried out as required by the Quality Assurance system and verify that all checks and test have been performed.

3. You will complete the investigation of complaints, initiating corrective and preventive actions.

4. You will also perform audits of API sites, Testing Laboratories and Release Sites whilst also performing self-inspections, ensuring compliance.

Role Requirements

To be successful in your application to this exciting opportunity as the Qualified Person (QP)l we are looking to identify the following on your profile and past history:

1. Relevant degree in a Science or QA discipline and registered as a Qualified Person (QP)

2. Proven industry experience gained as a QP on a manufacturing licence as well as QMS process design, implementation, management and utilisation experience

3. A working scientific knowledge and practical experience with GMP, with the ability to interpret and translate GMP guidelines into effective processes and procedures

Key Words: QP / Qualified Person / GXP / GMP / QA / Quality / Quality Assurance / QMS / Audits / Auditing / Batch Release / Directives 2001/83/EC / Quality Management / SOP / MIA / GDP
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.