Chemist II (12 hours shift)
Core
Perform testing and analysis of raw materials, in-process samples, and finished products to ensure product quality and regulatory compliance in a GMP environment.
Role type
Quality Control Chemist (Analytical)
Builds
Analytical solutions and quality release data for pharmaceutical raw materials, intermediates, and products
Domain
Pharmaceutical manufacturing / Quality Control
Required skills
GMP compliance, analytical techniques, method validation, technical documentation, data review, stock management, problem solving
Preferred skills
continuous improvement, project work, cross-functional communication
Technologies
state-of-the-art analytical equipment
Responsibilities
Perform transfer/verification/validation of laboratory procedures; prepare technical documentation including protocols and SOPs; analyze incoming goods and finished products under cGMP; review analytical data for accuracy and compliance; write up laboratory investigations and deviations; manage QC chemical and consumable stock levels; participate in practical process improvement initiatives.
Seniority
Mid-level, hands-on IC
