Cleaning Validation Specialist

MANTU GROUP SA; Guelph; On-site; CAD 60,000 - 100,000; Full time

Job summary

An innovative consulting firm is seeking a mid-level Cleaning Validation Consultant to support urgent validation activities at a manufacturing site. This hands-on role demands flexibility and proactivity, as the consultant will draft and execute cleaning validation protocols following an FDA audit. Collaborating closely with QA and Operations teams, the consultant will ensure regulatory compliance while being available for on-site activities, including nights and weekends. Join a dynamic team where your expertise will directly impact the success of critical projects.

Qualifications

• 4-6 years experience in Cleaning Validation in a GMP-regulated environment.
• Ability to write clear and compliant Validation Protocols.

Responsibilities

• Draft and review Cleaning Validation Protocols per cGMP and FDA.
• Execute cleaning validation activities for various equipment.

Skills

Cleaning Validation

Validation Protocols

cGMP Knowledge

FDA Requirements

Documentation Practices

Job description

Who are we?

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.

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

We are currently looking for aCleaning Validation Consultantwith mid-level experience to support urgent validation activities at our client’s manufacturing site in Guelph. The project follows a recent FDA audit and requires immediate support for protocol drafting and execution of cleaning validations across multiple equipment.

This is a hands-on role for consultants who are flexible, proactive, and comfortable working on-site, including nights and weekends as needed.

Key Responsibilities

• Draft and review Cleaning Validation Protocols in accordance with cGMP and FDA expectations.

• Execute cleaning validation activities for a variety of equipment and manufacturing systems.

• Collaborate closely with QA, Validation, and Operations teams to ensure proper documentation and alignment with regulatory standards.

• Support documentation practices and conformance reviews.

• Be available for on-site activities, including outside of regular working hours (24/7 operation site).

Requirements

• 4–6 years of experience in Cleaning Validation in a GMP-regulated environment.

• Demonstrated ability to write clear and compliant Validation Protocols and reports.

• Knowledge of Current Good Manufacturing Practices (cGMP) and FDA requirements.

• Availability to be on-site in Guelph regularly.

• Willingness to work night shifts or weekends if needed.

• Fluent in English (spoken and written).