Added
21 hours ago
Type
Full time
Salary
Salary not provided

Related skills

ms office lims hplc eln uv

๐Ÿ“‹ Description

  • Perform routine, non-routine and stability testing on finished pharmaceutical products
  • Utilise analytical techniques (primarily HPLC, Dissolution, Karl Fischer)
  • Support technology transfers and analytical development/validation activities
  • Review data for GMP compliance and manage OOS investigations when required
  • Document data per client policies and prepare results
  • Maintain productivity metrics and support audits and QC testing

๐ŸŽฏ Requirements

  • Degree in Chemistry, Analytical Chemistry or related field; significant GMP experience may be
  • Strong knowledge of analytical chemistry and HPLC; experience with dissolution, Karl Fischer and UV
  • Experience in pharmaceutical testing labs (solid dose preferred) and GMP environment
  • Proficiency with ELNs, LIMS and MS Office; able to work independently and in a team
  • Flexible approach, able to switch priorities, and focus on quality and customer service
  • Excellent written and verbal communication with stakeholders and customers

๐ŸŽ Benefits

  • Competitive rewards and recognition scheme
  • Holiday entitlement and health cash plan
  • Life assurance and company pension
  • Employee assistance programme and volunteering opportunities
  • On-site car parking and access to Perkbox
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