Bachelor's degree in a relevant field such as life sciences or engineering., Experience in quality assurance and regulatory compliance in the medical device or pharmaceutical industry., Strong understanding of FDA regulations and ISO standards., Excellent communication and analytical skills..
Key responsibilities:
Ensure compliance with regulatory requirements and quality standards.
Prepare and submit regulatory documents to authorities.
Conduct internal audits and quality assessments.
Collaborate with cross-functional teams to address quality issues.
Report This Job
Help us maintain the quality of our job listings. If you find any issues with this job post, please let us know.
Select the reason you're reporting this job: