About the Company
With an extensive range of fully qualified analytical equipment available, as well as comprehensive stability studies expertise, we work closely with our partners to assist every stage of the product development process. We have expertise in pharmaceutical analytical method development and validation, performing stability studies and QC product testing.
About the job
Intern will assist in the recommissioning and set-up of an analytical lab on site in the Midlands.
Student will work on quality system, ERP system and sourcing standards, facilitating contractors on site and developing SOPs.
Responsibilities
To update an existing laboratory in preparations for ISO17025 compliance. This role does not expect compliance to be achieved, just to scope, gap analysis, and implementation of primary requirements of the standard/QMS.
Requirements
Qualifications: Degree in a life Science discipline with Regulatory or Quality focus.
Desired: Knowledge of HPLC/UPLC, GC, Dissolution testing, laboratory management systems; GLP/QMS