QC Supervisor
Core
Provide leadership within Quality Control ensuring compliance with cGMP standards and regulatory requirements for pharmaceutical manufacturing from raw materials to finished products.
Role type
QC Supervisor
Builds
Pharmaceutical products and quality assurance processes
Domain
Pharmaceutical manufacturing / Quality Control
Required skills
cGMP compliance, FDA regulations knowledge, analytical testing methods, HPLC/GC operation, team leadership, technical writing, laboratory operations management, LIMS proficiency, project management, risk assessment, root cause analysis
Preferred skills
Chemistry/Biology/Biochemistry/Microbiology degree, quality systems certification, regulatory compliance certification, project management certification
Technologies
HPLC, GC, dissolution testing equipment, LIMS, quality management software, Microsoft Office
Responsibilities
Provide technical leadership and oversight for laboratory operations, mentor staff, optimize workflows, implement continuous improvement initiatives, support regulatory audits and inspections, manage laboratory scheduling and resource planning, lead investigations and problem-solving
Seniority
Mid-level, hands-on IC with leadership responsibilities
