Poslané v: Iné v New York City | Posted: |
Job Description
This Supervisor role leads and facilitates the operations of the Manufacturing Services team in line with all safety, regulatory and operational requirements. They assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build an inclusive culture of high performance for the team.
Oversee equipment maintenance, calibration, facility services, and production support which includes, but not limited to manufacturing, QC Lab, and R&D work areas. Includes equipment and site modifications, equipment installations, clean room mechanical operation, support production, splitter blade grinding, and removal of medical wastes.
Ensure all maintenance, calibration, and production support events and procedures are compliant with AbbVie procedures and regulatory standards (FDA/ISO).
Support root cause failure analysis program with Reliability Engineers as needed. Attend weekly downtime meetings with corporate reliability team to address equipment downtime on critical production equipment. Key contributor to all audits, including FDA, ISO, customer, and internal audits.
Prepare and report on monthly equipment KPIs that feeds into corporate’s Maintenance Excellence Program. Ensure production is supported with consumable equipment materials as needed (clean air cylinders/Solujet). Reconcile internal Medical Waste logs with Medical Waste Vendor disposal reports.
Address department’s (Production Support, Mfg. Services & Facilities) non-conformance, investigations and CAPA actions. Support corporate and site Maximo team projects and backup to Mfg. Services for corporate MEP and Perfect index reports. SME and site administrator for Maximo.
Provide off-hour support (on-call) to ensure base business needs are met.