A company is looking for a Quality Compliance Associate to provide compliance functions and project support within the Quality Compliance department.
Key Responsibilities
Prepare and update SOP documents and manage Quality Management Systems
Assist with audit scheduling, logistics, and document preparation for compliance audits
Support special projects related to CAPA document management and Learning Management System documentation
Required Qualifications
Bachelor's degree or equivalent work experience
1 - 2 years of relevant experience in a regulated pharmaceutical or medical device industry
Proficient in Microsoft Office Suite and SharePoint
Preferred experience with Standard Operating Procedures and project support
Ability to maintain confidentiality and work independently
Associate Compliance • Grand Rapids, Michigan, United States