Quality Assurance Associate

CK Group; Liverpool City Region; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading recruitment agency is seeking a GMP Quality Assurance Associate for a 12-month contract. This hybrid role, based in Speke, involves ensuring compliance with quality standards in the pharmaceutical industry. Candidates must have a scientific degree and experience in GMP quality operations. The position offers £19.23-£25.09 per hour. Applicants need to hold the right to work in the UK and should be prepared for a DBS check.

Qualifications

• Scientific Degree or equivalent in a relevant field.
• Experience in GMP quality operations.
• Excellent command of English, with other languages being an asset.

Responsibilities

• Perform QA oversight on assigned external suppliers and third parties.
• Monitor third party KPIs for compliance issues.
• Review and assess external customer complaints.

Skills

Experience in quality operations in the GMP environment

Excellent command of English

Knowledge and understanding of regulatory requirements

Good knowledge in office tools (Word, Excel, SAP)

Education

Scientific Degree or equivalent in Chemistry, Biology, Pharmacy or Pharmaceutical Engineering

Job description

CK Group are recruiting for a GMP Quality Assurance Associate to join a company in the animal health and pharmaceutical industry on a contract basis for 12 months.



Salary:

£19.23-£25.09 per hour PAYE



GMP Quality Assurance Associate role:

• Perform QA oversight on assigned external suppliers and third parties manufacturing products, ensuring that the delivered products comply with quality standards and legal requirements.
• Monitor third party KPI’s to proactively detect and notify to QA management any compliance issue on supplier level that would risk supply of products.
• Review and assess external customer complaints in the global complaint system, including Root Cause Investigation correctness, product impact assessment, trend/recurrence evaluation, and proposed CAPA assessment.
• Review batch release documentation provided by third parties to support or act as Authorized Person for release of products for shipment including material status change in SAP.
• Request timely annual Pharmacovigilance statements for PQRs.

Your Background:

• Scientific Degree or an equivalent in Chemistry, Biology, Pharmacy or Pharmaceutical Engineering.
• Experience in quality operations in the GMP environment.
• Excellent command of English, other languages are an asset.
• Knowledge and understanding of regulatory requirements.
• Good knowledge in office tools (e.g. Word, Excel, SAP).

Our client specialises in animal health. They advance their vision of food and companionship, enriching life by developing innovative solutions that protect and enhance animal health.



Location:

This role is based at our clients' site in Speke on a hybrid basis (2 days on site, 3 days work from home).



Apply:

For more information, or to apply for this GMP Quality Assurance Associate role, please contact the Key Accounts Team on 01438 870011 or email [e-mail]. Please quote reference 148 925.



It is essential that applicants hold entitlement to work in the UK



Please note:This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.



INDKA