Sr. Quality Engineer Medical Devices

Our client is a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. It is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in the US, this company employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public. 

 

This Sr. Quality Engineer will be responsible for supporting new product development and product maintenance through the application of Quality Engineering skills. This requires the ability to handle multiple projects and tasks from product inception through product launch and maintenance.

The Quality Engineer will play an active role in the processes to ensure products meet the quality standards consistent with company policies, while meeting all design control and other regulatory requirements. Participates as Quality Representative on Design and Manufacturing Project teams. Supports plant activities in the areas of process validation, process capability and customer issues. Supports/initiates Corrective and Preventative action with an eye to increased capability and customer satisfaction.  Bachelors degree in Engineering or related Science. CQE, CQA and/or RAC certification desirable or achievement within first 2 years. 3-5 years Quality experience or 10+ years of related experience in the medical device or pharmaceutical industry is desirable.

 



 PLEASE SUBMIT RESUME IN WORD FORMAT TO:  jhudson@appleassoc.com  and dwink@appleassoc.com .

 

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