Req ID:
Remote Position: No
Region: Europe
Country: Ireland
State/Province: Galway
City: Galway
General Overview
Band 07 - Specialist, Operations Quality
Req ID:
Remote Position: No
Hiring Manager: Enda Cleary
Band: 07
Region: Europe
Country: Ireland
State/Province: Galway
City: Galway
Summary
The primary purpose of this position is supervising and co-ordinating the activities of a production team – Operators & Technicians, to ensure that all assembly/production of all scheduled products is accomplished in conformance with quality, cost, time and to the customer's satisfaction.
Detailed Description
1. Organisation and co-ordination of a production team to manufacture quality product on schedule and in a safe and efficient manner
2. Initiate and drive production and quality improvement projects in line with the principles of Lean Manufacturing
3. Identification & optimum allocation of production resources, i.e., people, equipment, time, maintenance & calibrations
4. Completion of timely performance reviews and appraisals
5. Develop a strong team culture of Engagement, Inclusion and Innovation through communication and team leadership
6. Management of the Company Time and Attendance System for direct reports
7. Provide direction and support to manufacturing team members
8. Grievance / disciplinary / corrective action case management
9. Ensure that good housekeeping is maintained
10. Ensure that all employees are adequately trained to Quality and EHS procedures
11. Ensure that employees are aware of and comply with all company policies and procedures
12. Meet all requirements of QMS – to a high standard, in a medical device manufacturing environment.
13. Engage and participate on delivery of all the Business Unit KPl's
14. Work with other departments to ensure cross functional goals are satisfied
15. Daily communication with customer to ensure quality, schedules and deliveries are met
16. Maximise efficiencies and performance on production cells
Knowledge/Skills/Competencies
17. Competency in a range of skills associated with your primary work area and possesses and actively uses coaching and some additional key skills outside of their primary work area.
18. Dynamic individual with a 'can do 'attitude, prepared to take responsibility, be flexible and motivated.
19. Good knowledge of product process flow.
20. Ability to recognise problems in the assembly process and to address those problems.
21. Ability to learn established quality and quantity requirements.
22. Ability to work effectively with team members and lead the team to high quality production within tight deadlines.
23. Knowledge of personal computers and ability to learn and use applications specific to this area.
24. Ability to maintain detailed, accurate and organised records.
25. Knowledge of and adherence to Quality/ISO audit requirements.
26. Ability to effectively communicate with a variety of internal customers (external also, if applicable).
27. Excellent communication, inter-personal and team skills
28. Demonstrated organisational and planning abilities
29. Strong leadership and people management skills
30. Customer focused
Physical Demands
31. 5+ years' experience in an operations environment.
32. Experience working in a Medical Device Manufacturing cleanroom environment is essential
33. Previous Production Supervisory Experience or Coordinator experience at a minimum.
34. Relevant qualification e.g., Supervisor Management and/or people leading experience desirable.
35. Good People management and communication skills.
36. Experience working in a target driven environment.
37. Good working knowledge of MRP & experience working with SAP system
38. Computer literate and working knowledge of Microsoft packages.
Typical Education
39. Bachelor's degree in related field, or consideration of an equivalent combination of education and experience.
40. Educational Requirements may vary by Geography
Notes
This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.
Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.
COMPANY OVERVIEW:
Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.
Celestica would like to thank all applicants, however, only qualified applicants will be contacted.
Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.