Supervisor, Manufacturing - 3rd Shift Sun to Fri

Supervisor, Manufacturing - 3rd Shift Sun to Fri
Supervisor, Manufacturing - 3rd Shift Sun to Fri
Mentor, Ohio, United States
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 Productivity.
The 3rd Shift Supervisor role supports production onsite in our Mentor, OH facility.Hours are Sunday 10:30 pm through Friday 6:30 am (5 days a week, 8 hour shifts).
Must arrive 15 -20 minutes earlier for the hand off from the previous supervisor, and to stay 15-20 minutes after the shift to hand off to the next supervisor.
Occasionally attend leadership training or other meetings during the day shift every few months.
What You'll do as a Manufacturing Supervisor (3rd 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 (SQDP) 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, leads investigations 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 (SQDP) performance.
Trains, audits, improves standard work, and implementing daily kaizen activities to meet SQDP 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 SQDP 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.

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.

Experience with a medical device or regulated environment a plus.
Proficiency with MS Office applications such as Excel, PowerPoint and Word).
Experience with Material Requirements Planning (MRP) systems such as Oracle or similar systems.

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

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
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

Pay range for this opportunity is $70,000 to $85,000. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits:
Open until position is filled.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit .
If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location’s HR Office during normal business hours.
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