Steris Manufacturing

**Position Summary **

The Supervisor, Manufacturing is responsible for planning, organizing, and supervising daily production activities, and ensuring that products are delivered in accordance with Customer requirements, while complying with applicable company, quality, and regulatory standards. The supervisor will train and coach production employees in creating and sustaining a lean culture aligned with the company’s Vision, Mission and Values. By utilizing key leadership principles of respect, humility, and leading by example, the supervisor will create a positive work environment by engaging employees in the continuous improvement of Safety, Quality, Delivery, and Cost initiatives.

**The 2nd

Shift Supervisor role supports production onsite in our Mentor, OH facilityMonday through Thursday 3:00pm to 1:30am (Four 10 -hour days). **

**What You’ll do as a Manufacturing Supervisor -2nd Shift**

• Ensures attainment of daily/weekly production plan by ensuring communication between the cells / shifts, sharing best practices, prioritizing countermeasures among production cells and ensuring proper job performance of all team members.
• Drive attainment of and improvements in safety, quality, delivery, and cost (SQDC) performance.
• Meets Customer needs through creative solutions. Responds with a sense of urgency and aligns activities, focusing on the needs and requirements of the Customer.
• Leads with proper adherence to quality system procedures, Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP).
• Ensures immediate response to abnormalities through identifying, documenting, and segregating nonconforming material.
• Monitors process flow; identifies solutions for flow interrupters and ensures immediate response to abnormalities and/or on signals while exhibiting a detailed understanding of processes and equipment.
• Monitors operational status on all equipment/tools including calibration and certification, escalates as needed.
• Facilitates a safety culture, performs safety audits to ensure proper use and condition of Personal Protective Equipment (PPE), machines, and safeguards, trains individuals on safety procedures and expectations, leadsinvestigations of near misses / incidents and facilitates the implementation of safety and ergonomics improvements.
• Learns and teaches others the basic lean principles and tools.
• Teaches, coaches and leads problem solving methodologies and tools to improve safety, quality, delivery and cost (SQDC) performance.
• Trains, audits, improves standard work, and implementing daily kaizen activities to meet SQDC objectives.
• Provides daily coaching of Team Leaders and Operators on job duties and explanations of the "why" behind Lean principles and tools.
• Executes, audits, and drives continuous improvement of 5S in department according to STERIS standards.
• Champions idea generation system across department through providing support to team members in generating and implementing ideas. Ensures idea generation board is updated and best ideas implemented are presented weekly to facility management.
• Challenges current state, seeking opportunities to make incremental improvements daily and identifying solutions to remove waste from production activities.
• Drives optimum employee performance, talent and talent development. Provides growth, training, and development opportunities to employees. Drives results through effective coaching, and counseling of staff and setting meaningful and measurable goals.
• Evaluates performance and escalates needs through proper managing and coaching of team members in relation to SQDC board meetings and daily standard reports (daily production, material requirements, etc.).
• Screens and selects qualified individuals for positions, conducts performance reviews, determines salary adjustments, work schedules, promotions, training, and effectively addresses employee relations situations and manages conflict.
• Covers Team Leader absences to maintain flow and efficiency of work area.

**The Experience, Skills and Abilities Needed**

Required:

• Associate’s degree and a minimum of 2 years of manufacturing operations experience, preferred.
• In lieu of a degree, a high school diploma /GED and a minimum of 8 years’ experience in manufacturing operations.
• Minimum of 2 years of supervisory experience.

Preferred:

• Experience with a medical device or regulated environment a plus.

**What STERIS Offers **

*We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future. *

*Here is just a brief overview of what we offer: *

• Market Competitive pay
• Extensive Paid Time Off and added Holidays
• Excellent Healthcare, Dental and Vision benefits
• Long- and Short-Term Disability coverage
• 401(k) with a company match
• Maternity and Paternity Leave
• Additional add- on benefits / discounts for programs such as Pet Insurance
• Tuition Reimbursement and continuing education programs
• Excellent opportunities for advancement in a stable long-term career

You should be proficient in:

• Leadership / People Management
• FDA Regulations
• Supervisory Experience
• Good Manufacturing Practices (GMP)

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