Salary :
Activity area : Pharmaceutical and medical
Post category : Scientific and technical positions
With a core expertise in development and manufacturing of medical devices, our client is dedicated to providing innovative and safe devices. The company places a strong emphasis on compliance, quality assurance, and patient safety through cutting-edge technology and rigorous testing.
They are looking for a quality assurance associate that will be involved in maintaining the integrity of the quality system documentation in compliance with ISO 13485 standards. With 3-5 years of experience in the medical device industry, the candidate will be responsible for managing configuration, document control, and change control processes. Key responsibilities include supporting audits, regulatory inspections, product testing, and onboarding new employees in the eQMS environment.
The ideal candidate will also contribute to continuous improvement efforts within the Quality Management System (QMS), helping ensure product safety and regulatory compliance across various stages of development and production.
Skills and qualifications :