Pharmaceutical Cleaning Validation Specialist
Amaris Consulting
Date: 3 days ago
City: Toronto, ON
Contract type: Full time
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
Are you passionate about pharmaceutical manufacturing and ensuring the highest standards of cleanliness and compliance? We are currently looking for Cleaning Validation Specialists to join our growing team in Toronto! If you're open to new opportunities and excited to be part of a collaborative, high-performing environment, we'd love to hear from you.
Responsibilities:
Lead and support cleaning validation activities across manufacturing areas
Write and execute cleaning validation protocols and reports (IQ/OQ/PQ)
Perform risk assessments and define cleaning strategies in line with cGMP and regulatory requirements
Collaborate cross-functionally with QA, Manufacturing, and Engineering teams
Investigate and resolve cleaning-related deviations and non-conformances
Maintain documentation aligned with FDA, EMA, and other global regulatory standards
Requirements:
Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, or related field
Proven experience in cleaning validation within the pharmaceutical or biotech industry
Strong knowledge of GMP, FDA/EMA regulations, and cleaning validation guidelines
Experience with protocol writing, execution, and data analysis
Excellent problem-solving skills and attention to detail
Strong communication and teamwork abilities
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
Are you passionate about pharmaceutical manufacturing and ensuring the highest standards of cleanliness and compliance? We are currently looking for Cleaning Validation Specialists to join our growing team in Toronto! If you're open to new opportunities and excited to be part of a collaborative, high-performing environment, we'd love to hear from you.
Responsibilities:
Lead and support cleaning validation activities across manufacturing areas
Write and execute cleaning validation protocols and reports (IQ/OQ/PQ)
Perform risk assessments and define cleaning strategies in line with cGMP and regulatory requirements
Collaborate cross-functionally with QA, Manufacturing, and Engineering teams
Investigate and resolve cleaning-related deviations and non-conformances
Maintain documentation aligned with FDA, EMA, and other global regulatory standards
Requirements:
Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, or related field
Proven experience in cleaning validation within the pharmaceutical or biotech industry
Strong knowledge of GMP, FDA/EMA regulations, and cleaning validation guidelines
Experience with protocol writing, execution, and data analysis
Excellent problem-solving skills and attention to detail
Strong communication and teamwork abilities
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