Manufacturing Supervisor

Description

Job Summary: Responsible for maintaining operational compliance, planning and organizing resources, ensuring product quality, and fostering an optimal work environment in medical device manufacturing. Key Highlights: 1. Leadership in medical device manufacturing 2. Team management and continuous improvement 3. Focus on quality and regulatory compliance Description and details of responsibilities 1\. Maintain operational compliance based on regulations for manufacturing drug dispensers, vital signs monitors, and instrumentation, with strict adherence to all applicable procedures within the assigned area. 2\. Build production models according to priorities reflected in the Production Schedule. 3\. Plan, organize, and allocate resources within the assigned production area in accordance with required demand, ensuring product availability aligned with customer demand. 4\. Ensure appropriate documentation is available during product assembly and packaging. 5\. Monitor implementation of methods and process changes. 6\. Supervise product assembly and packaging to ensure compliance with quality specifications. 7\. Maintain control for product traceability and counting during assembly, packaging, and shipping. 8\. Responsible for monitoring and decision-making regarding process control on assigned production lines. 9\. Actively participate with the MRB or improvement teams in root cause investigations and implementation of corrective actions as required to resolve out-of-specification conditions and/or inefficient or non-conforming operations. 10\. Motivate staff to create an optimal work environment and foster teamwork. 11\. Maintain team morale and discipline within a positive and constructive atmosphere that drives highly productive operations and continuous improvement. 12\. Maintain safety, as well as promote and practice the 5S program (Sort, Set in order, Shine, Standardize, Sustain). 13\. Provide training and implement training programs for Production Department personnel. 14\. Maintain documentation of certification progress and individual performance evaluations for direct reports. Experience and Requirements * Bachelor's degree and professional title * Prior experience in this position, preferably in the medical device contract manufacturing industry. * Advanced English * Advanced * Preferred knowledge of Six Sigma/DMAIC tools. * Willingness to face challenges and commitment to the philosophy of continuous improvement Benefits * Benefits in accordance with the Federal Labor Law (LFT) * Life insurance * Savings fund * Medical expense insurance * Savings box * Guaranteed profit-sharing * On-site medical services **Number of vacancies** 1 **Department** Operations **Contract type** Permanent **Work modality** On-site **Shift** Day shift **Working hours** Full-time **Education** Bachelor's degree with professional title **English proficiency** Spoken: 90%, Written: 90% **Willingness to travel** Yes