Coloplast
This role involves performing quality inspections on implantable medical devices throughout the manufacturing process, from incoming materials to finished goods. The incumbent is responsible for preparing and releasing sterile surgical loads while ensuring strict compliance with FDA QMSR and ISO 13485 documentation requirements. Responsibilities include managing calibration assistance, maintaining equipment, processing rejected materials, and supporting production quality resolution.
Coloplast is a global medical device company that develops and manufactures products and services for people with intimate healthcare needs. Their offerings span ostomy care, continence care, interventional urology, bowel care, wound and tissue repair, and voice and respiratory care. They serve over 2 million people annually across more than 100 countries, and also provide support services for both patients and healthcare professionals.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Coloplast.
36% below the average for this role