QC Specialist - new job in Speke, UK

Job title: QC Specialist - Global Pharmaceutical company

Contract: 12 months contract

Location: Speke, UK

SRG are working with a global pharmaceutical company to help them find a QC Specialist to join their busy team.

As a QC Specialist you will be accountable for Liverpool QC method validation lifecycle, method transfers and improvements. You wil be Reporting to the Analytical Science and Technology manager and the role is accountable for Quality Control method validation lifecycle management and method standardisation/robustness.

The QC specialist is an SME in testing methodology, able to troubleshoot technical issues, develop current and existing methods and be current with the latest analytical testing technologies. The role requires the execution of intra site method transfers and SME input into regulatory filings/audits. The role will involve GMP execution of development and technical assays in support of both egg and cell characterisation samples.

Key Responsibilities will include:

• Maintain the compliant status of QC method validation lifecycle.
• Trouble shoot technical challenges with QC test methods.
• Execution of method standardisation and robustness program
• Development of current and new test methods. Engaged with the latest testing technologies
• Execution of intra site method transfers and SME input into regulatory filings/audits

Candidate Requirements:

• BSc or MSc in scientific field
• At least 2 years industrial experience
• Experienced in a GMP environment
• Experience of Quality Control testing techniques and industry practices

To apply click the link or send your CV

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