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