Pharmaceutical Laboratory Expert

5 days ago


Loughborough, Leicestershire, United Kingdom Kindeva Drug Delivery Full time

Job Summary

We are seeking a skilled QC Stability Analyst to support Kindeva's QC Stability Group. The ideal candidate will have experience in writing stability protocols, setting up stability studies, and generating reports to support stability testing in a GMP-compliant laboratory.

Responsibilities

  • Support the development and implementation of quality control processes
  • Collaborate with cross-functional teams to ensure seamless execution of stability studies
  • Maintain accurate laboratory records and adhere to relevant standards and procedures

Requirements

  • BTEC HND with 3-5 years of relevant experience
  • 240 OU points in a relevant discipline
  • Previous experience working with GLP, GMP, Specifications, and Test Methods
  • Able to interpret analytical data and write effective stability protocols and reports

Estimated Salary: £45,000 - £55,000 per annum (dependent on experience)

What We Offer

  • Competitive salary and benefits package
  • Ongoing training and development opportunities
  • Opportunity to work with a talented team of professionals


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