Senior Quality Analyst/Quality Manager (DOE)
Validation of equipment - KF, HPLC, Mass Spec, FTIR etc
Stability work - manage the stability programme.
Purification work when required
Assist in audits when needed and represent QC
Method development projects and method validation projects
The company is only small and they are looking for someone to 'own' the QC area and want to develop themselves and the QC area as the company grows.
Skills and Experience
Analytical experience in a pharma GMP environment
Methods validation and /or development experience of HPLC methods
Supervisory experience an advantage
You must have the right to work in the UK. Learn more
- Agency: SRG
- Reference: J2160227
- Posted: 21st September 2021
- Expires: 19th October 2021