Job Title: Quality Assurance Specialist
This role requires a skilled professional to oversee the validation of new products, equipment qualification, and site requalification programs.
Key Responsibilities:
* Design, execute, and report on PV/Process Performance Qualifications
* Develop and implement validation strategies for equipment, systems, and processes
* Ensure validation studies are managed in accordance with all relevant industry standards and regulations
* Provide technical guidance on current regulatory requirements
* Maintain accurate documentation throughout the validation lifecycle
Requirements include a degree in Science or Engineering, 3-5 years experience in a regulated manufacturing environment, and knowledge of pharmaceutical plants and process validation regulations.
The ideal candidate will have excellent analytical and problem-solving skills, as well as strong communication and project management abilities.