At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.
Position SummarySupports manufacturing functions to produce medical devices in a FDA regulated and
controlled environment. Provides support to Supervisor and department employees
to achieve safety, quality, delivery, and cost requirement
BENEFITS:
Shift: 2:30pm-10:30pm Monday - Friday
Benefits: Healthcare, Vision, Dental, 401K Match, Quarterly Bonuses, PTO, Company Holidays
Duties1. Problem solve process deviations and equipment issues through observations.
2. Assist Supervisor with electronic editing of time clock entries, SQDC Board Updates,
5S Audits, Idea Board (Encourage and implement ideas), Value Stream meeting and
SQDC Board presentation.
3. Follow Team Lead standard work, observe assemblers standard work
4. Prepare for and/or lead start-up and shift-end handoff meetings.
5. Maintain strong lines of communication with all applicable personnel across all shifts.
6. Able to effectively train employees on standard work and operating procedures within
the department. Perform observations to flex matrix (level 2 and 3), perform TWI audits
7. Work with the Supervisor to manage and assign daily work schedule and job duties to
employees.Ensure schedules are followed and changes are communicated across all
shifts
8. Audit HRXHR boards,collect reasons codes,record shift totals, shift recap
9. Activate, set-up and operate labeling equipment, autobaggers, robots, welder, laser,
etc. (as applicable to department).
10. Complete and turn in accurate paperwork on time to meet Build schedule
11. Communicate raw material stock levels as needed.
12. Promote and provide a safe working environment.
13. Promote an effective working team environment.
14. Know, adhere to, and reinforce Shop Practices including proper gowning and use of
personal protective equipment.
15. Participate/look for opportunities to hold problem solving huddles
16. Develop and complete IDP (Individual Development Plan) objectives
17. Participate and support Kaizen events
18. Perform sorting, rework, and production as needed
19. Attend/complete required training courses by specified due dates
20. Perform other duties as needed.
Education Degree High School Diploma or GED Required ExperienceMust have at least five years manufacturing experience assembling small parts and/or leadership
experience
STERIS is a leading provider of products and services that meet the needs of growth areas within Healthcare: procedures, devices, vaccines and biologics. We exist to fulfill our MISSION TO HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD. STERIS is a $3B, publicly traded (NYSE: STE) company with approximately 16,000 associates and Customers in more than 100 countries. 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 and the use of affirmative action programs 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.