As the QA Supervisor – PQR/CPV you will be responsible for the coordination, preparation, and review of PQR and CPV reports along with documentation such as Annual Reviews, Validation Protocols and Reports
Job Summary
As the QA Supervisor – PQR/CPV you will be responsible for the coordination, preparation, and review of PQR and CPV reports along with documentation such as Annual Reviews, Validation Protocols and Reports.
Develop and maintain a competent, motivated, and engaged team through effective communications, management, recruitment, training and development.
Viatris strives to create a positive, productive work environment where integrity, dignity and mutual respect for all is ingrained each and every one of us.
Matching Summary
As the QA Supervisor – PQR/CPV you will be responsible for the coordination, preparation, and review of PQR and CPV reports along with documentation such as Annual Reviews, Validation Protocols and Reports.
Skills & Requirements
Must-have
Product Quality Review
Continued Process Verification
Annual Reviews
Validation Protocols and Reports
GMP environment
technical documents
Nice-to-have
building rapport and relationships
managing competing priorities
positive productive work environment
highly inclusive organization
Key Requirements
Tertiary qualifications in Science and/or similar
Previous experience in pharmaceutical industry
Experience managing and supervising professional employees