ATS Company: ATS Corporation Requisition ID: 12987 Location: Cambridge, ON, CA, N3H 4R7 Date: Sep 18, 2024 Quality Engineering Job Description MAJOR DUTIES: Responsible for the operation of quality processes, applications and analysis of data using statistical methods to diagnose and correct non-compliance situations. Develop and administer data information systems and audit quality systems for deficiency identification and correction requirements in conjunction with other business disciplines using a cross-functional approach. GENERAL RESPONSIBILITIES • Ensure that all business activities are performed with highest ethical standards and in compliance with ATS code of business conduct. • Adhere to all Health and Safety rules and procedures. • Comply with all ATS Policies / Procedures / Instructions as per the ATS Quality Systems. • Ensure that all business activities are performed in accordance with the ATS Confidentiality Policy. • Lead or Participate in Continual Improvement Activities SPECIFIC RESPONSIBILITIES: • Analyze and report data used to monitor quality performance to ensure customer requirements are met. • If applicable, conduct training of personnel with regards to internal procedures. • Prepare Control Plans, and support update of Procedures or Checklists as applicable. • Co-ordinate Product FAI’s and verification of supplier parts. • Participate or lead external audits and witness testing at suppliers’ facilities, if appropriate. • Investigate product / process quality issues. Initiate Customer Initial Complaint Notifications (CICN) as appropriate. • Act as a facilitator, as well as a team member for corrective action or 8D activities. • Conduct internal product, process and procedure compliance audits, as appropriate. • Maintain good relationships with all functional groups and locations within the Company by participating in functional and multi-functional teams. • Maintain good relationships and liaison with external customers and suppliers on Quality related matters. • Perform trend analysis on Quality data and identify required corrective actions • Support program launch and FAT activities. • Support the Implementation as required of error proofing initiatives based on trend analysis perform on long term programs. • Perform other duties as related to those outlined above, or which may be completed based on individual skill or experience. Additional Information QUALIFICATIONS: Education: Graduate Engineer or Technologist or equivalent work experience (4 years min.) ASQ CQE certification preferred Experience: • Five (5) years’ experience in a manufacturing environment • Demonstrated ability to work independently and to manage multiple projects from various diverse organizations • Lean and/or Six Sigma Experience is an asset. • Strong problem-solving skills. • Ability to work as part of a cross-functional team. • Understanding of change management principles and Change Agent Skills. • Microsoft Excel, Word, PowerPoint – Intermediate level. • Working knowledge of ISO requirements – 9001 and 13485 • Current trained Internal ISO Auditor is considered an asset. • Highly developed attention to detail. • Working knowledge of Automation and / or Medical Device industry quality requirements. • Excellent verbal and written communication skills. • Excellent reading comprehension. • Proficient at Blueprint reading. • Training in GDP and GMP • Knowledge of measurement techniques. Able to interpret CMM reports • Capable of performing basic measurements using hand tools is required, CMM programming capability is an asset