Hello, I am planning to apply for Express entry PR. I am working as a Validation associate in pharmaceutical industry. I am confused regarding my NOC code. Can someone please give me some guidance on this? My job duties are as follows.
Writes and executes installation, operational and performance qualification protocols for
critical production equipment, utilities and processes.
Scheduling, planning, managing and executing studies for clean validation.
Writes detailed validation reports and analyzes complex quality data.
Maintains revalidation schedules ensuring the facility remains in a validated state.
Co-ordinate with other departments and schedule training associated with process
validation, cleaning validation and equipment validation/qualification.
Writes and reviews SOP’s related to qualification activities.
Works directly with clients to understand and create qualifications.
Reviews vendor supplied protocols and documentation for accuracy and compliance
with internal requirements.
Participate in investigation associated with validation activities and manufacturing
process related challenges.
Troubleshoots and rectifies issues.
Thorough understanding of FDA, ICH and 21CFR guidelines to perform validation
activities as per regulatory and compliance requirement.
Supporting regulatory submissions and also regulatory agency inspections whenever
required.
Works closely with cross-functional departments as necessary to resolve issues.
Performs other duties as assigned.
Writes and executes installation, operational and performance qualification protocols for
critical production equipment, utilities and processes.
Scheduling, planning, managing and executing studies for clean validation.
Writes detailed validation reports and analyzes complex quality data.
Maintains revalidation schedules ensuring the facility remains in a validated state.
Co-ordinate with other departments and schedule training associated with process
validation, cleaning validation and equipment validation/qualification.
Writes and reviews SOP’s related to qualification activities.
Works directly with clients to understand and create qualifications.
Reviews vendor supplied protocols and documentation for accuracy and compliance
with internal requirements.
Participate in investigation associated with validation activities and manufacturing
process related challenges.
Troubleshoots and rectifies issues.
Thorough understanding of FDA, ICH and 21CFR guidelines to perform validation
activities as per regulatory and compliance requirement.
Supporting regulatory submissions and also regulatory agency inspections whenever
required.
Works closely with cross-functional departments as necessary to resolve issues.
Performs other duties as assigned.