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Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
What you will do
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.
What you will need
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.