Develop, validate, and transfer analytical methods for active pharmaceutical ingredients and finished dosage forms within Pharco's Analytical R&D department. You will support formulation teams and regulatory submissions with high-quality analytical data.
Key Responsibilities
Develop HPLC, UPLC, and spectroscopic methods for drug substances and drug products
Execute method validation studies per ICH Q2(R1)
Author analytical sections of regulatory dossiers and technical reports
Support technology transfer of analytical methods to QC laboratories
Maintain and calibrate laboratory instruments in compliance with GLP
Requirements
B.Sc. or M.Sc. in Analytical Chemistry, Pharmacy, or related field
3+ years of analytical method development in a pharma or CRO environment
Hands-on proficiency with HPLC, UV-Vis, IR, and dissolution testing equipment
Understanding of ICH Q2 method validation guidelines
Proficient in English technical writing
Nice to Have
Experience with hyphenated techniques (LC-MS/MS)
Knowledge of Empower or similar chromatography data systems
Familiarity with ICH Q14 analytical procedure development guidance
