At Amaris, we strive to provide our candidates with the best possible recruitment experience. We like to get to know our candidates, challenge them, and be able to give them proper feedback as quickly as possible. Here's what our recruitment process looks like:
Brief Call: Our process typically begins with a brief virtual/phone conversation to get to know you! The objective? Learn about you, understand your motivations, and make sure we have the right job for you!
Interviews (the average number of interviews is 3 - the number may vary depending on the level of seniority required for the position). During the interviews, you will meet people from our team: your line manager of course, but also other people related to your future role. We will talk in depth about you, your experience, and skills, but also about the position and what will be expected of you. Of course, you will also get to know Amaris: our culture, our roots, our teams, and your career opportunities!
Case study: Depending on the position, we may ask you to take a test. This could be a role play, a technical assessment, a problem-solving scenario, etc.
As you know, every person is different and so is every role in a company. That is why we have to adapt accordingly, and the process may differ slightly at times. However, please know that we always put ourselves in the candidate's shoes to ensure they have the best possible experience.
We look forward to meeting you!
Job description
Are you an experienced CQV professional looking to contribute to critical pharmaceutical projects? We are currently seeking CQV Engineers to join our growing team in Toronto! If you're open to exciting new opportunities and thrive in fast-paced, highly regulated environments, we’d love to hear from you.
Responsibilities:
✔ Lead and execute commissioning, qualification, and validation (CQV) activities for pharmaceutical equipment, utilities, and systems
✔ Prepare and review CQV documentation, including protocols (IQ/OQ/PQ), reports, and risk assessments
✔ Ensure compliance with GMP, FDA, EMA, and other global regulatory standards
✔ Collaborate with cross-functional teams including QA, Engineering, Manufacturing, and Project Management
✔ Troubleshoot systems and support investigations for deviations and non-conformances
✔ Participate in FAT/SAT execution and system handover processes
Requirements: