Validation Engineering Co-op

Students MUST upload a transcript with previous work term ratings (if applicable) and portfolio. Applications missing required documents may not be considered.

This role is posted until May 18th at 11:59pm.

Within ATS Life Sciences Systems, what we do matters – we custom design, build and service critical automated solutions for medical device and pharmaceutical companies. Our customers are leaders in their industries and rely on us to deliver what we promise; to bring products to market faster with the highest quality. Together with our broad product range, financial strength, and global footprint, we provide the best automation solutions to our customers.
 
Our Validation Engineering team is looking for a motivated and ambitious student who thrives in a challenging but rewarding environment. Join our team!

• Position Title: Validation Engineering Co-op
• Department: Validation Engineering
• Reports To: Validation Manager
• Duration: 4 or 8 months (September – December or April)
• Location: Cambridge, ON (Onsite)
• Range: $20.44 - $30.43

Why Join ATS?

• Be a part of a global organization that is an industry-leading automation solutions provider to many of the world’s most successful companies
• Working on challenging engineering projects
• A chance to contribute to something bigger - advancing the future of healthcare through automation
• Work with other bright, talented people and discover opportunities for professional growth
• Comprehensive training including formal study and mentoring within your team
• Subsidized breakfast and lunch daily; free gourmet beverages - coffee, tea and hot chocolate. Plus, treat day is every other week!
• Receive five vacation days
• Half-Day Fridays
• Ability to participate in a variety of charitable events
• Social club that offers social events throughout the year
• Fully equipped production facilities that are clean, quiet and climate controlled  

ATS is in compliance with the Accessibility for Ontarians with Disability Act (AODA), 2005 and will, upon request, assist those who may require specific accommodations due to a personal disability. We would ask that those who require assistance to notify our offices as soon as possible if accommodation is necessary.  

Job Description

Job Summary:

Gather information, update Validation test protocols, supporting documents and project-related technical documentation. In addition, the candidate will have to have an understanding of how the various pieces of automated equipment operate and understand the principle of Validation and Engineering.

Job Responsibilities:

• Work with technical and engineering personnel to update validation related documentation.
• Perform test execution on shop floor.
• Record and collect data gathered during test execution using Good Documentation Practices.
• Contribute to development of validation documents, test protocols and machine functional specifications.
• Organize and record project related documentation received internally and from customers.
• Assist in the coordination and delivery of all validation documentation provided to customers, including printed and electronic copies.
• Ensure that accurate records of all documentation delivered to customers are kept.
• Ensure that project records are kept and archived in accordance with ATS procedures.
• Assist with the development and updates of customer and internal validation, machine acceptance test protocols and supporting documents.
• Adhere to all aspects of the department procedures.
• Perform other duties as assigned.
• Occasional overtime and weekend work may be required.
• Ensure that all business activities are performed with the highest ethical standards and in compliance with the ATS Code of Business Conduct.
• Adhere to all health and safety rules and procedures.
• Contribute to the development and maintenance of internal standards.

Education:

• Working towards a post-secondary degree specializing in Systems Design, Electrical, Controls, or Mechanical Engineering program

Required Skills:

• Knowledge of computer programs such as Windows, Excel, Word, Outlook and Project.
• Working knowledge of AutoCAD and SolidWorks as well as some understanding of PLC programming software like RS Logix or Siemens
• Technical understanding of pharmaceutical / biotechnology unit operations is helpful
• Technical understanding of general automation equipment design and principles.
• Strong communication and interpersonal skills.
• Some exposure to cGMP requirements and current industry practices.
• Demonstrate ability to work in a cross-functional team environment.
• The ideal candidate will possess excellent planning and coordination skills and be able to readily adapt to changes in priorities and project schedules.
• Prior experience with automation equipment, equipment validation and project engineering would be an asset.

Health, Safety, and Environmental

All employees have the responsibility to work in a safe manner and report any health, safety or environmental concern to their manager or supervisor in a timely manner.

Health, Safety and Environment include:

• Work in compliance with divisional health, safety and environmental procedures
• Refrain from removing or altering safety devices or guarding unless hazardous energies are controlled through lockout-tagout methods
• Report any unsafe conditions or unsafe acts
• Report defect in any equipment or protective device
• Ensure that the required protective equipment is used for the assigned tasks
• Attend all required health, safety and environmental training
• Report any accidents/incidents to supervisor
• Assist in investigating accidents/incidents
• Refrain from engaging in any prank, contest, feat of strength, unnecessary running or rough and boisterous conduct