Validation Specialist at ATS Automation Tooling Systems Inc
Cambridge, ON, Canada -
Full Time


Start Date

Immediate

Expiry Date

01 Nov, 25

Salary

0.0

Posted On

03 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Windows, Equipment Design, Excel, Continuous Improvement, Coordination Skills, Chemistry, Autocad, Project Engineering, Outlook, Unit Operations, Rslogix, Development Programs, Interpersonal Skills, Aoda, Physics

Industry

Electrical/Electronic Manufacturing

Description

ATS Company: Life Sciences Systems
Requisition ID: 15359
Location:Cambridge, ON, CA, N3H 4R7
Date: Jul 31, 2025

EDUCATION:

  • Bachelor’s degree in science (engineering, physics or chemistry preferred) or equivalent experience and greater than 3 years of directly related experience.

EXPERIENCE:

  • Technical understanding of pharmaceutical / biotechnology unit operations.
  • Technical understanding of general automation equipment design and principles.
  • Strong communication and interpersonal skills.
  • Good knowledge of cGMP requirements and current Life Science industry practices (ISPE C&Q Guidance and GAMP5).
  • 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, Life Science equipment validation and project engineering would be an asset.
  • Experience with Windows, Excel, Word, Outlook and Project. Should have some understanding of AutoCAD and Solid works as well as PLC programming software like RSLogix or Siemens Step 7.
  • Ability to travel in the USA and Europe
    If you’re excited about this role, but do not meet all the qualifications listed above, you are still encouraged to apply
    Why YOU should join our ATS Life Sciences Systems team:
    We value our PEOPLE - The foundation of a great company is having the best team which is why we continuously work to develop, engage, empower and energize our people. The best people want to work with the best team - the best teams are diverse and inclusive teams.
    What we do MATTERS - our Life Sciences projects contribute to improving the lives of people around the world! ATS has made a commitment to be carbon neutral by 2030!
    INNOVATION and PROBLEM SOLVING is at our core - Our pursuit of continuous improvement in everything we do. Our focus is on building diverse teams, stimulating innovation by challenging conventional thinking, encouraging fresh ideas and promoting creative problem-solving
    We prioritize internal GROWTH & DEVELOPMENT - ATS offers endless opportunities for professional growth and development – with a tuition reimbursement program, individual development programs and a commitment to promoting from within - there is space for you to grow your career at ATS!
    We offer COMPETITIVE Total Rewards - Competitive starting salaries, overtime pay eligibility, paid vacation, Employee Incentive Bonus program, comprehensive health and dental benefits including Lifestyle Spending Account, 5% RRSP matching program and optional Employee Share Purchase Program
    A place to BELONG: We celebrate our differences and ensure that all employees have equal opportunities for growth and development. We believe that diversity of thought, background, and experiences is essential for our success and innovation.
    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
Responsibilities

MAJOR DUTIES:

Provide the coordination, creation and execution of validation activities including (but not limited to) writing protocols, performing qualifications, review of documents that support the manufacturing of automated equipment on large single module custom machines or large multi-module custom systems or replication projects. In addition, the candidate will understand how the various pieces of automated equipment operate and understand the principle of Life Science Validation and Engineering.

SPECIFIC RESPONSIBILITIES:

  • Administer, create, maintain, and execute validation plans, procedures, and protocols for projects.
  • Work with technical and engineering personnel to prepare and create validation related documentation and functional specification documentation.
  • Develop and design custom test plans for projects based on similar projects and templates and engineering knowledge
  • Lead review meetings with the internal team and customers to review and approve validation related documentation
  • Organize, lead and report on validation efforts at both ATS and at the customer’s site.
  • Read and examine the schematics, blueprints, electrical drawings and confirm the electrical wiring connections of industrial equipment as per design.
  • Execute installation qualification to verify installation and function of e-stops, guard doors, safety switches, feeders, safety light curtains, contactor, relays, HMI, pneumatic regulators, fiber-optic and coaxial cable sensors, switchboard meters and other electrical components at ATS and occasionally at customer sites.
  • Verify testing of electrical utilities including current, voltage and panel ratings. Perform continuity testing on digital inputs and outputs, using PLC access, multimeter or visual check.
  • Perform the installation qualification and operation qualification to test the instrumentation devices, vision system, PLC, electrical motors, and other hydraulic and pneumatic electrical control systems.
  • Use the PLC, VFD, HMI and other electrical control system components to trigger faults and machinie alarms in order to verify machine programming and fault handling.
  • Conduct the calibration of industrial instruments or evaluate and maintain the calibration records.
  • Lead the generation and completion of any deviations, equipment and document change control resulting from testing, qualification and /or validation activity.
  • Take a validation project lead role for the duration of a project lifecycle, including being a primary validation contact for customers, ATS project managers and other project stakeholders and coordinating additional validation team members assigned to the project
  • Assist in defining and implementing acceptance criteria, specifications, and standards for each qualification activity.
  • Ensure that all business activities are performed with the highest ethical standards and in compliance with the ATS Code of Business Conduct.
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