Opportunity to join a global medical device company currently going through a transition and investing heavily into the Quality team.
Responsibilities
Develop and improve inspection methods to analyze product quality
Improve product quality by making recommendations for change
Work together with relevant teams and departments to improve products
Ensure products adhere to company and industry quality standards
Own and execute to the company non-conforming process
Document results and findings after inspections are carried out
Implement a working system to ensure conformity and accuracy in the production process
Own and/or execute to the company CAPA process
Develop Process Validation protocols
Qualifications
7 years' quality experience in the Medical Devices space and familiarity with 21CFR820 and ISO:13485
Bachelor's degree in engineering preferred
High proficiency in computer technology and systems operations
Excellent verbal and written communication skills