Qc Stability Analyst

NextPharma Technologies

Livingston, GB
On-site
Cgmp, fda and mhra regulated environment
Hplc, gc, dissolution, kf, wet chemistry
Stability testing of finished products
The role will primarily be responsible for the conducting of stability analytical activities for technical, clinical. and commercial products

Job Summary

  • The role will primarily be responsible for the conducting of stability analytical activities for technical, clinical. and commercial products.
  • Must be technically competent in analytical activities (e.g. pharmacopoeail wet chemistry, HPLC, GC, Dissolution, KF) for stability testing of finished products.
  • We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway.

Matching Summary

The role will primarily be responsible for the conducting of stability analytical activities for technical, clinical. and commercial products.

Skills & Requirements

Must-have

  • cGMP, FDA and MHRA regulated environment
  • HPLC, GC, Dissolution, KF, wet chemistry
  • Stability testing of finished products
  • Writing stability summaries, protocols and reports
  • Ordering lab supplies
  • Company health and safety procedures

Nice-to-have

  • Results oriented with a positive outlook
  • Solid planning and organizational ability
  • Reliable, tolerant and dependable
  • Comfortable dealing with senior managers
  • Enjoy working in a fast, stimulating environment
  • Pragmatic approach to problem solving

Key Requirements

  • HNC/HND/Science Degree or Equivalent
  • 2-3 years experience in pharmaceutical/biotech
  • Permanent Right to Work in the UK

Work Rights

Must have permanent Right to Work in the UK

Tailored Resume

Cover Letter