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© All Rights Reserved. ApplyBlast.com
Coloplast
This role supports the Value Stream by performing inspections of incoming, in-process, and finished goods while preparing and releasing surgical sterile loads. The position ensures that all documentation and Device History Records (DHRs) comply with FDA QMSR and ISO 13485 requirements. The inspector is responsible for verifying production records, managing quarantined materials, and collaborating with engineers to resolve quality issues.
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.
6% above the average for this role