Oversees and coordinates the activities in a production area to meet production goals, quality and cost objectives while setting and/or prioritizing production schedules based on product introduction, equipment efficiency and materials supply. Implements production and large-scale manufacturing procedures in a production environment in order to optimize processes and meet regulatory requirements. May review existing operational and process discrepancies in manufacturing and provide technical expertise to improve procedures.

• Ensure continuous compliance with all regulatory requirements, including FDA and COFEPRIS standards.

• Stop production if non-conforming products are identified, ensuring continuous workflow.

• Supervise and coordinate team activities to meet quantity, quality, and efficiency goals.

• Monitor production costs, efficiency, and key performance indicators (KPIs) to maintain cost-effectiveness.

• Manage timecards, payroll adjustments, and approve time-off requests for each employee.

• Promote engagement and lead initiatives to meet or exceed business performance indicators.

• Ensure all employees adhere to EHS procedures, minimizing environmental, health, and safety risks.

• Train or coordinate the training of team members, while coaching and developing direct reports.

• Address personnel and production issues, participate in staffing reviews, and lead continuous improvement efforts.

• Prepare regular performance reports and participate in operational meetings as a liaison between team and management.

• 2+ years related manufacturing environment or experience in a regulated industry.

• Engineering or other Professional Degree or Equivalent Experience.

• Experience in Medical devices industry preferable.

• Intermediated English.

• Proficient in Microsoft Office suite (including Word, Excel and Power Point).

• Good communication and supervisory skills.

• Availability to work in the 2nd Shift (night shift), or any other shift for future opportunities.