Job Opportunity

Reference: QS0768
Title: Method Development Analyst
Location:
Northampton  
Job Type:
Full time permanent
Salary: £19,000 -
£25,000 per annum
Contact Person: Miss Selina Thompson 0113 225 1547
apply@qualitystart.co.uk

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 apply@qualitystart.co.uk quoting the reference number and the job title.

 

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