Pharmaceutical - Cleaning Validation Specialist
1 month ago
**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.
**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.
We look forward to meeting you
**Job description**:
We are looking for dynamic consultants to grow our **Life Science Team** in **Toronto**. Your experience, knowledge, and commitment will help us to face our client's challenges.
You will be supporting different projects through your expertise as a **Pharmaceutical - Cleaning Validation Specialist.**
**Your main responsibilities**:
- **Develop and maintain the Validation Master Plan**: Create and maintain a plan documenting the cleaning validation procedures.
- **Perform risk analysis**: Identify and assess risks associated with cleaning to develop mitigation strategies.
- **Prepare validation protocols**: Draft detailed protocols describing the specific procedures for cleaning validation tests.
- **Execute tests and analyze results**: Oversee cleaning tests and analyze results to ensure the effectiveness of procedures.
- **Prepare validation reports**: Document the results of cleaning tests in detailed reports to comply with regulatory standards
**Qualifications**:
- Less than 5 years of experience
- **Validation Master Plan**:
- **Validation protocols/ Validation reports**:
- Cleaning & Decontamination / Sterilisation (**CIP/SIP**)
- Hold Time (**CHT**) / Dirty Hold Time Time (**DHT**) / Intermediate Hold Time (**IHT**)
- **Sampling**:
- **P&IDreading**:
- Fluent in English both written and spoken
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