Hyper Recruitment Solutions
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Quality Specialist

Experience Dependant
Job Reference: J5631465
Updated On: 09/05/2019
Status: Open to Applications
Hyper Recruitment Solutions
Sectors: Pharmaceutical

Skills: Quality Assurance - Contract, Quality Assurance - GMP, Quality Assurance - ISO9001

Job Information

Role Overview

We are currently looking for a Quality Specialist to join a leading Pharmaceutical company based in the Cambridgeshire area for a 6 month contract. As the Quality Specialist you will be responsible for maintaining the QMS and ensuring GMP compliance is maintained throughout the business's operations associates to assigned products.

Key Duties and Responsibilities

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

1. You will ensure GMP compliance is maintained across the businesses operations, this will involve liaising with internal and external departments including CMO's to process Quality Documentation (Batch Record Reviews, Validation Documentation, PQR's and Quality Technical Agreements).

2. The Quality Specialist will maintain the Change Control system, investigate Customer Complaints and agree effective actions in response to Quality related issues to maintain compliance.

3. You will play an active role in regulatory inspections, internal audits and customer audits and participate in both customer and supplier management activities including maintaining supply chain activities.

4. Maintain and develop company Quality Systems to build a strong Quality Culture throughout the business, you will support the Head of Quality in delivering effective GMP training as well as review and update relevant SOP's.

Role Requirements

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

1. Relevant degree in a Scientific Discipline or related technical experience.

2. Proven industry experience in the Pharmaceutical Industry working in a QA Role in a GMP compliant environment.

3. A working knowledge and practical experience with the Pharmaceutical Manufacturing Process/ CMO activity would be advantageous.

Key Words: Pharmaceuticals | GMP | cGMP | Quality Assurance | QA | Sterile | Licensed Medicines | Quality Management System | Change Control | CAPA's | Deviations | Supplier Management | Compliance | Audits | Specialist | Associate| Quality | GDP | Good Distribution Practice | Vendor Assurance | GXP | GLP | Compliance | Documentation | QA Officer | Senior QA Officer | QA Associate |
Aliyah Iheanacho
Your Recruitment ConsultantAliyah IheanachoAliyah.Iheanacho@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.