The role involves leading a team of 12 analysts to ensure the timely and high-quality execution of microbiological quality controls for medicines, raw materials, and packaging
Job Summary
The role involves leading a team of 12 analysts to ensure the timely and high-quality execution of microbiological quality controls for medicines, raw materials, and packaging.
Candidates must possess strong leadership skills to foster a positive team culture while maintaining strict adherence to national and international GMP guidelines.
The supervisor acts as a spokesperson during audits and inspections, responsible for reviewing and authorizing critical QC GMP documentation including protocols and reports.
Matching Summary
The role involves leading a team of 12 analysts to ensure the timely and high-quality execution of microbiological quality controls for medicines, raw materials, and packaging.
Skills & Requirements
Must-have
Microbiological analysis techniques
GMP regulatory compliance knowledge
Team leadership of 12 analysts
CAPA incident investigation
QC documentation review and authorization
Nice-to-have
Experience in pharmaceutical production environment
Inclusive leadership style
Subject matter expertise in cross-functional projects
Proactive and flexible mindset
Strong relationship building with internal clients
Key Requirements
Master or Bachelor degree in Microbiology, Biotechnology, or Biochemistry
Leadership experience within a pharmaceutical quality organization
Experience with authority inspections and cGMP regulations