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 :

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
Il y a plus de 30 jours