AS Engineer

SHL Medical; Deerfield Beach (FL); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Competitive compensation package

Modern working environment

Opportunities for personal and professional development

Job summary

A leading medical device company located in Deerfield Beach, Florida, is seeking a qualified individual to execute tests and analyze data in the medical device industry. You will be responsible for running design assessments, ensuring compliance with quality standards, and preparing documentation. Candidates must hold a B.E. in Biomedical Engineering or related fields, have 1–2 years experience in medical devices, and proficiency in Microsoft Office. Join our dynamic team committed to innovation and quality.

Qualifications

• 1–2 years of experience within the medical device industry is required.
• Familiar with FDA, ISO, and ASTM guidelines.

Responsibilities

• Execute Design Assessment, Design Verification, Test Method Validation and Transfer tests.
• Run tests using lab test equipment.
• Perform root cause analysis of non-conformance findings.
• Comply with quality, safety, and work rules.

Skills

Design Verification practices

Good Laboratory Practices

Good Manufacturing Practices

Proficiency in Microsoft Excel

Proficiency in Microsoft Word

Effective communication

Ability to work in teams

Education

B.E. in Biomedical Engineering/Mechanical Engineering

Job description

SHL Medical is a world‑leading provider in the design, development, and manufacturing of advanced self‑injection devices. With a global team of 6,000 employees, we partner with leading pharmaceutical and biotech companies to deliver innovative autoinjectors, pen injectors, and other drug delivery systems that ensure effective treatment for patients. Headquartered in Switzerland since 2018, with key operations in Sweden, Taiwan, and the US, we are united by a commitment to innovation, impact, and growth. Together, we empower our people to develop solutions that make a meaningful difference in the lives of millions of patients while fostering a supportive, inclusive, and dynamic workplace for our colleagues.

Job Overview

Execute tests, document & analyze test data, write protocols, procedures, equipment work instructions, test instructions.

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 be a key member of a cross‑functional team that will conduct “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.
• Various opportunities for personal and professional development within a global organization.