Validation Medior

**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**:
**Job description**:
Join our team and start a new adventure in an international and dynamic environment where you will be able to fulfill your career expectations in a fast-growing organization.

As a **Quality Support Specialist** within the Life Sciences division, you will be part of a multidisciplinary team ensuring compliance and operational excellence for laboratory equipment management.
- Your missions
- Provide QA support for the management of laboratory equipment within Vx CL&AP and HBSMCT in the Rx-86 facility.
- Oversee QA follow-ups on equipment-related requests, including:

- Approval of documents related to validation, qualification/requalification in line with procedural requirements.
- Calibration & measurement plans/maintenance schedules.
- Review and approve deviations/non-conformities and associated CAPAs linked to laboratory equipment, ensuring adherence to procedural standards.
- Identify quality risks and opportunities and escalate appropriately.
- Represent the Quality department in multidisciplinary meetings and project governance.
- Your profile
- Experience with analytical equipment and IT validation.
- Knowledge of deviation and CAPA management.
- Familiarity with analytical biological testing processes.
- Proficiency in SAP, LEM, or Binocs is an asset.
- Minimum 5 years of experience in a relevant role.
- You demonstrate strong analytical and problem-solving skills.
- What we offer
- An international community bringing together 110+ nationalities.
- An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities.
- A robust training system with our internal Academy and 250+ available modules.
- A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.).
- Strong commitments to CSR, notably through participation in our WeCare Together program.