In this role, the selected candidate will ensure service quality and participates in care coordination to ensure proper communication between caregivers, patients, referral sources and payers; discuss operational issues, update staff on new/changed regulations and review records/documentation to ensure regulatory and in-house compliance.
In this role, the selected candidate will resolves conflicts within the group relating to performance and/or workload, ensures proper resource allocation within and across teams, over-site of timesheet review and the planning and scheduling spreadsheet.
In this role, the selected candidate will direct complex technical and/or organizational problem solving activities using proven tools such as Root Cause Analysis, Statistical Analysis, screening experiments, Design of Experiments (DOE), etc.
In this role, you will oversee the development, implementation, or tech transfer of all methods for testing and release of inprocess, and release testing for biological products and reference materials.
In this role, the selected candidate will act as a compliance resource to provide guidance and assistance towards resolution of moderate to complex deviations, quality investigations, lab investigations, CAPAs and change control.
This QA/RA role is responsible for supporting R&D project teams through the New Product Development process for various medical devices at Hill-Rom's Acton MA Business site. This position will also be responsible for participating on various Design Assurance improvement initiatives to improve the overall quality of new product designs and the company's regulatory compliance profile per 21CFR820 regulations.