Job Information
MALLINCKRODT Manufacturing Supervisor Medical Device in MADISON, Wisconsin
JOB REQUIREMENTS: Job TitleManufacturing Supervisor, Medical Device Requisition JR000014188 Manufacturing Supervisor, Medical Device (Open) Location CC-Madison - USA503 Additional Locations Madison, WI Job Description The Manufacturing Supervisor, Medical Device or is responsible for on the floor oversight of day-to-day manufacturing operations to ensure the performance, productivity, and efficiency of the production team. Responsible for supporting the overall GMP Manufacturing process through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production area. The Manufacturing Supervisor, Medical Device will be responsible for leadership of operations hourly team members. In addition, this role will work closely with the Supply Chain team, Sustaining Engineering, Manufacturing Engineering, and Quality to ensure work conforms to company quality systems, ISO 13485, and customer and company requirements are met. Essential Functions Review production orders, production schedules, visible parts supplies, and other reports to provide production completion estimates against ongoing business goals. Provide operational leadership for day-to-day cGMP device manufacturing production and activities. Perform and document all assembly, test and repair work per established work rules, policies, and procedures. Work with Manufacturing, Supply Chain, Quality Assurance, and Management teams to effectively troubleshoot to assure customer requirements can be met. Collaborate with Quality Assurance to ensure Production processes and methods are maintained on the floor and within compliance. Assist in development and revisions of Standard Operating Procedures (SOP), Work Instructions (WI) device history records, or other quality documentation, as necessary, to support production processes. Provide continuous improvement suggestions for methods, technology, utilization of time and resources to help the team more effectively achieve business goals and objectives. Perform initial review and/or final sign-off of executed cGMP documentation such as batch production records, deviations, or forms, as needed. Support team with ongoing coaching, training,... For full info follow application link. Mallinckrodt Pharmaceuticals provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetics. In addition to federal law requirements, Mallinckrodt Pharmaceuticals complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/96C4913008CD4B9B