What are the responsibilities and job description for the Complaint Handling Specialist position at DEKA Research & Development?
DEKA R&D has an immediate opening for a Complaint Handling Specialist to work in a dynamic Medical Device Research and Development environment. The position reports to the Product Complaints Manager. This is a role with direct impact to the Quality Management System.
How you will make an impact :
- Responsible for reviewing medical complaints that involve a potential quality problem.
- Perform product complaint evaluations independently while also collaborating with other team members.
- Ensure that complaint documentation follows Good Documentation Practices; meets QMS requirements; and complies with U.S. Food and Drug Administration (FDA) regulations / other regulatory requirements.
- Identify and make sound decisions regarding medical device reporting to regulatory agencies.
- Influence the creation of new procedures and work instructions.
- Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory agencies.
- Participate in CAPA investigations as they relate to complaint handling.
- Maintain positive and cooperative communication with co-workers, customers, contractors, and vendors.
- Perform other related duties as assigned under management supervision.
Skills needed to be successful :
About DEKA :
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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