We are looking for a diligent professional to maintain the excellence and regulatory compliance of our biopharmaceutical products. The successful candidate will be responsible for ensuring quality assurance standards are upheld, facilitating inspections and audits, and supporting continuous improvement initiatives within our state-of-the-art manufacturing facility.
Key Responsibilities
* Quality Assurance Oversight: Develop and maintain quality procedures, policies, and systems. Conduct routine self-inspections and monitoring assessments to ensure compliance with regulations.
* Regulatory Compliance: Stay current with industry regulations and best practices. Assist in preparing and executing regulatory inspections and audits.
* Documentation and Reporting: Maintain accurate and comprehensive quality records, change control documentation, and quality reports.
* Process Improvement: Identify areas for process improvement and work collaboratively with cross-functional teams to implement changes.
Bachelor's degree in Science, Engineering, or Quality-related discipline. 3+ years of experience in quality assurance within a biotechnology, pharmaceutical, or medical device manufacturing environment.