Overview

Quality Engineering Jobs in Cambridge, Ontario, Canada at ATS Automation

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

Title: Quality Engineering

Company: ATS Automation

Location: Cambridge, Ontario, Canada

Category: Quality Assurance – QA/QC (Quality Engineering, QA Specialist / Manager, Quality Control / Manager)

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