AS Engineer

Job Overview

Main Responsibilities

• Execute Design Assessment (DA), Design Verification (DV), Test Method Validation (TMV) and Test Method Transfer (TMT) tests.
• Run tests using lab test equipment such as Instron, vibration machine, environmental chambers, etc.
• Perform root cause analysis of non-conformance findings and participate in cross-functional teams conducting "out of specification investigations."
• Record and analyze test results against requirements.
• Prepare operational procedures, work instructions and test instructions.
• Help with/initiate document updates.
• Assist the QA Engineer in all quality activities to support the Analytical Sciences department.
• Comply with all quality, safety, and work rules and regulations.

Skills and Qualification

• Preferred B.E. in Biomedical Engineering/Mechanical Engineering or any relevant branch of study.
• 1–2-year experience within the medical device industry is required.
• Candidate must be familiar with current Design Verification practices and guidelines including those required / outlined by the FDA, ISO, and ASTM.
• Knowledge of Good Laboratory Practices, Good Manufacturing Practices & Good Documentation Practices.
• Proficiency in Microsoft Excel and Microsoft Word is a must.
• Able to communicate effectively and work within cross-functional teams.

We Offer

• Competitive compensation package
• Modern working environment with state-of-the-art facilities and technologies
• Challenging assignments in a fast-growing and innovative industry
• Position in a dynamic, international team of highly skilled professionals
• Variety of opportunities for personal and professional development within a global organization

How we hire

• Once you’ve applied, it may take up to three weeks to review your application and get the first call with a recruiter.
• Our recruitment process is focused on allowing you to show your personality, experience and competencies while giving you a great sense of who we are.