Pharmaceutical - Quality Control Specialist

3 weeks ago

Montréal, Canada Amaris Consulting Full time

**Who are we?**:
**Amaris Consulting** is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1000 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 6000 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 Sciences **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 **Quality Control Specialist.**

**Your main responsibilities**:

- Investigate nonconformities and determine corrective and preventive actions (CAPA)
- Perform cGMP compliant testing as required to support Raw Material testing, In-process, Finished Product Release & Stability
- Perform routine QC analysis (e.g. ELISA, UPLC/HPLC, CGE, GC, Particulates)
- Contribute to SOPs, protocols, technical studies, and reports
- Perform preventative maintenance / calibration on basic laboratory equipment in accordance with established procedures
- Support the development of Quality Systems in collaboration with on-site and global quality teams.

**Qualifications**:

- Bachelor's degree or diploma in chemistry, biology or related field of study.
- 4+ years of related experience in a pharmaceutical cGMP environment
- Knowledge of pharmaceutical GLPs and GMPs
- Understanding of MS Office, LIMS, SAP would be an asset
- Knowledge of FDA, Health Canada regulations and ICH guidelines
- Demonstrated ability to work effectively in a team
- Excellent communication skills in English

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