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Engineer, Quality Engineering

Job in Deerfield Beach, Broward County, Florida, 33441, USA
Listing for: SHL Medical Assembly&Servc LLC
Full Time position
Listed on 2026-07-13
Job specializations:
  • Engineering
    Quality Engineering, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 65000 - 85000 USD Yearly USD 65000.00 85000.00 YEAR
Job Description & How to Apply Below
Position: AS Engineer

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.

Performs root cause analysis of non-conformance findings and will 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

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