Formulation Chemist Ii/Laboratory Supervisor
Current• Pharmaceutical topical development and cGMP manufacturing. • Review and prepare GMP batch records, product quality control specifications, and stability testing documentation. Write change controls and deviations. • R&D batch preparation and toxicology batch preparation (GLP).• Laboratory notebook documentation and technical writing.• Manage and execute multiple projects assigned.• Source formulation ingredients and materials. Partner with suppliers.• Process development and optimization. • Assist in day-to-day manufacturing operations and supervise batch production in a GMP environment. • Troubleshoot equipment and manufacturing issues. • Supervise general laboratory operations, including material purchasing and inventory management, equipment acquisition, qualification and maintenance, and creation of Standard Operating Procedures. • Collaborate with chemist and quality unit to maintain the lab’s daily work functions and meet deadlines.• Understand and implement lean concepts and 5S methodology.• Train and schedule staff, write performance reviews and approve time cards. • Resolve problems, identify the root cause, and propose improvements to senior management.