Job Opportunity

Reference: QS0768
Title: Method Development Analyst
Job Type:
Full time permanent
Salary: £19,000 -
£25,000 per annum
Contact Person: Miss Selina Thompson 0113 225 1547

Opportunity: Do you have experience in analytical method development and validation? Have you managed analytical method transfer projects? Want to work for a growing pharmaceutical company? Yes then this is the role for you!

Your role as a Analytical Development Validation Analyst based in Northampton will involve developing analytical methods and method validation working to relevant cGMP, ICH and USP standards.

Duties and responsibilities include:

  • Execution of Analytical Method Validation as per ICH Q3 guidelines.
  • Analytical method transfer as per USP<1224> guidelines.
  • Execution of Analytical Method Verification as USP <1226> guidelines.
  • Planning, execution and monitoring of analytical method validation / verification.
  • Problem solving analytical method issues.
  • Developing of stability indicating analytical methods for assay, related substances and residue methods on UPLC and HPLC.
  • Reviewing method validation / verification protocols for API, in process and finished product analytical methods.
This is a full time permanent job opportunity paying between £19,000 - £25,000 per annum and great benefits.  There is a lot of career development as the company continues to grow. 

Skills: To apply for the Analytical Development Validation Analyst role you will have the following skills:

  • Degree qualified within a scientific subject.
  • Quality control analytical method development and method validation experience within the pharmaceutical or related industry working to cGLP / cGMP standards.

How to Apply: In order to apply for this vacancy please ensure you have read and agree to the privacy policy found here and then email your CV to quoting the reference number and the job title.


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