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Quality Assurance Specialist

SRG
Posted 8 hours ago, valid for 10 days
Location

Sevenoaks, Kent TN13 2TH, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The job title is Quality Assurance Specialist, located in Kent.
  • The salary range for this position is £36,000 - £42,000.
  • Candidates are required to have proven QA experience in a GMP environment.
  • A degree in Chemistry, Pharmaceutical Sciences or a related field is also required.
  • The role involves maintaining the Pharmaceutical Quality System and supporting compliance with GMP/GDP standards.

Job Title: Quality Assurance SpecialistLocation: KentSalary: £36,000 - £42,000

SRG are recruiting for a Quality Assurance Specialist to join a growing pharmaceutical manufacturer based in Kent. This company specialises in the production and distribution of a diverse range of medicinal products, placing quality, compliance, and innovation at the heart of its operations.

The Role:

As a Quality Assurance Specialist, you will play a key role in maintaining and enhancing the Pharmaceutical Quality System (PQS) across the business. You will support compliance with GMP/GDP standards, regulatory frameworks, and contribute to the development of QA staff. This role is integral in ensuring the company's high standards are met and continuously improved upon.

  • Act as a Quality Specialist for the Business Unit, maintaining the QMS, manage change controls, deviation investigations and implantation & review of CAPAs
  • Support and prepare for audits, including regulatory inspections and supplier assessments.
  • Oversee batch record and label generation in alignment with production schedules
  • Lead Quality and Continuous improvement projects
  • Mentor QA Officers and support staff training in GMP/GDP matters

Requirements:

  • A Degree in Chemistry, Pharmaceutical Sciences or a related field, or equivalent practical experience
  • Proven QA experience in a GMP Environment.
  • Experience in supporting, preparing for or leading internal / External audits.
  • Validation Experience would be highly advantageous.
  • Attention to detail and the ability to manage multiple priorities.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.