Quality Assurance Specialist

1 week ago


Singapore Amaris Consulting 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.

**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**:
**Mission Description**:

- Oversee Quality compliance in validation processes, with an emphasis on Data Integrity.
- Collaborate with Subject Matter Experts to conduct gap analyses and risk evaluations prior to qualification efforts.
- Participate in investigations of validation discrepancies, aiding in the review and approval of discrepancy reports and ensuring CAPA closures.
- Review and authorize various validation documentation, such as protocols and reports.
- Provide assistance and solutions for validation-related inquiries and challenges.
- Evaluate and approve routine SOPs, forms, and other relevant documents, including Manufacturing Batch Records.

**Profile Requirement**:

- Background in Quality Assurance or Quality Control within a regulated setting.
- Familiarity with validation processes and principles of Data Integrity.
- Strong analytical and problem-solving capabilities.
- Excellent communication and collaborative skills.
- Can start by November.



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