Bachelor degree in chemical or pharmaceutical analysis
7+ years industry experience in analytical area
Expertise in hplc, ms, gc, aas, uv, ir, nir methods
The role requires managing instrument reports, leading critical deviations, and investigating Out-of-Specification (OOS) results within a pharmaceutical environment
Job Summary
The role requires managing instrument reports, leading critical deviations, and investigating Out-of-Specification (OOS) results within a pharmaceutical environment.
Candidates must possess deep technical expertise in various analytical methods including HPLC, MS, GC, and spectroscopy while ensuring strict GMP compliance.
The position involves preparing specifications for applications, leading change management projects, and acting as a Subject Matter Expert for the QC core system.
Matching Summary
The role requires managing instrument reports, leading critical deviations, and investigating Out-of-Specification (OOS) results within a pharmaceutical environment.
Skills & Requirements
Must-have
Bachelor degree in chemical or pharmaceutical analysis
7+ years industry experience in analytical area
Expertise in HPLC, MS, GC, AAS, UV, IR, NIR methods
Knowledge of analytical development, transfer and validation
Strict adherence to GMP compliance and SOPs
Experience with OOS investigation and deviation management
Nice-to-have
Fluent English communication skills
Strong team work spirit
Excellent computer literacy
Good presentation skills
Proactive sense of responsibility
Key Requirements
Minimum 7 years industry experience in analytical area
Bachelor degree in chemical, pharmaceutical or analysis subjects