Especialista De Validação Sênior (fixed Term: 12 Months)
Kenvue
Sao Jose dos Campos, Brazil
Hybrid
Manufacturing, packaging and cleaning validation
Scientific expertise in technical operations
Cgmp's, anvisa / cofepris / fda / ich regulations
The Validation Specialist 3 is responsible for providing a high degree of scientific expertise in Technical Operations for the delivery of manufacturing, packaging and cleaning validation projects for a broad range of OTC products
Job Summary
The Validation Specialist 3 is responsible for providing a high degree of scientific expertise in Technical Operations for the delivery of manufacturing, packaging and cleaning validation projects for a broad range of OTC products.
This individual collaborates cross-functionally with Operations, Quality Assurance, Research & Development and other functions to provide subject matter expertise and technical leadership in design, development and implementation of validation requirements.
Provide direction and mentorship to lower-level professionals within the organization, promoting adherence to all company guidelines related to health, safety and environmental practices.
Matching Summary
The Validation Specialist 3 is responsible for providing a high degree of scientific expertise in Technical Operations for the delivery of manufacturing, packaging and cleaning validation projects for a broad range of OTC products.
Skills & Requirements
Must-have
manufacturing, packaging and cleaning validation
scientific expertise in Technical Operations
cGMP's, ANVISA / COFEPRIS / FDA / ICH regulations
technical writing
statistical knowledge (DOE, process capability)
Nice-to-have
critical thinker with problem solving skills
interpersonal and influencing skills
emerging industry guidance for validation
Key Requirements
Bachelor’s degree in Chemistry, Pharmacy, Chemical Engineering or correlated areas
Experience with GMP validation
Experience in a highly regulated environment
At least intermediate English for reading and written communication