R&d Mfg Scientist Ii - Analytical Development

PPD (Thermo Fisher) UK

United Kingdom
Hplc and dissolution experience
Method development and validation
Good manufacturing practices (gmp)
Provides routine analyses in a biochemistry environment within defined procedures and practices

Job Summary

  • Provides routine analyses in a biochemistry environment within defined procedures and practices.
  • Lead the validation of test methods for pharmaceutical raw materials and finished products.
  • Develop methods and processes that meet or exceed the expectations from clients and provide innovation.

Matching Summary

Provides routine analyses in a biochemistry environment within defined procedures and practices.

Skills & Requirements

Must-have

  • HPLC and Dissolution experience
  • Method development and validation
  • Good Manufacturing Practices (GMP)
  • Laboratory setting with PPE required
  • Handling hazardous/toxic materials

Nice-to-have

  • Client meeting participation
  • Innovation in methods and processes
  • EMPOWER software experience

Key Requirements

  • Bachelor Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological science field minimally required with 3+ years related experience
  • Master’s degree, 1+ year related pharmaceutical industry experience strongly preferred
  • Good knowledge and understanding of chemistry and analytical instrumental technologies
  • Good knowledge of qualitative and quantitative chemical or microbiological analysis
  • Awareness of quality and regulatory requirements in the pharmaceutical industry

Work Rights

Not specified

Tailored Resume

Cover Letter