Quality Chemist required for a leading Pharmaceutical manufacturer .
Role will support testing of finished product across a variety of techniques for the solid oral dosage, sterile and biologic product portfolio.
Duties:
Review of analytical data and documentation to ensure compliance to appropriate specifications and protocols.
Supports reviews and investigations for out- of trends/outof specifications.
Participates in validation and commercial/developmental manufacturing activities Troubleshoots standard instrumentation/test methods.
Coordinates waste management, LEAN/Operational excellence and 5S efforts as required.
Participate in QC and cross-functional projects as required.
Writes and revises methods, specifications, and SOPs as needed.
Experience:
BSc degree in analytical Biochemistry or equivalent.
Prior experience in pharmaceutical industry is required Must have Chromatographic separations experience in UPLC/HPLC and Empower Technical writing (protocols, reports, procedures) The ability to analyse data with a logical approach to problem solving and troubleshooting Excellent spoken and written communication skills Proficient in Microsoft office Working knowledge of GMPs, GLPs, pharmacopeial, and regulatory requirements for testing and validation pertaining to the pharmaceutical industry is required.
Skills:
HPLC UPLC UV FTIR GMP GLP