Production Supervisor / Advanced Bionics
Sonova
Experience and Requirements Bachelor’s degree in Engineering, preferably in Industrial, Electronics, Mechanical, Electrical, Mechatronics, or Biomedical Engineering. Minimum of 3–5 years of experience supervising manufacturing assembly lines, preferably within the medical device and/or electronics manufacturing industry. Valid B1/B2 visa for travel to the United States. Demonstrated ability to take a leadership role, particularly when conducting production meetings and coordinating activities with Engineering, Planning, Quality Assurance (QA), and Research & Development (R&D). Experience performing production capacity analysis and generating reports to support production scheduling decisions and respond to operational requirements. Experience leading production meetings focused on performance metrics, floor training, production priorities, and Quality Improvement Teams (QIT). Knowledge of Line Clearance procedures and regulatory compliance requirements applicable to medical device manufacturing, including FDA 21 CFR requirements. Strong understanding of production schedules, material handling, inventory flow, and Lean Manufacturing principles. Experience working with ERP systems, preferably Dataflo, as well as Microsoft Access, Word, and Excel. Strong analytical, organizational, communication, and problem-solving skills. Ability to work effectively in a fast-paced manufacturing environment and collaborate with cross-functional teams. Preferred Qualifications APICS certification or related supply chain/manufacturing certification. Experience working in a Lean Manufacturing environment. Previous experience in an FDA-regulated manufacturing environment, preferably within the medical device industry. Experience with soldering, welding, or similar assembly processes. Experience with continuous improvement methodologies such as DMAIC, Kaizen, or Six Sigma.
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