Test Engineer​/Validation Engineer

Test Engineer/Validation Engineer

Kelly Services is currently seeking a Test Engineer/Validation Engineer position for one of our top clients in Danvers, MA.

As a Test Engineer placed with KellyOCG you will be responsible for the following:

In this role, you will be responsible for designing, executing, and validating tests to ensure products meet defined requirements, regulatory standards, and quality expectations. This position plays a critical role in supporting product development and maintaining compliance within a regulated laboratory environment.

• Execute testing activities in accordance with standardized guidelines, including FDA regulations, SOPs, and internal work instructions
• Design and perform verification testing to ensure products meet defined requirements and specifications
• Must have hands-on CAD experience and mechanical testing
• Analyze historical and current test data using statistical tools to identify trends and support decision-making
• Develop and maintain comprehensive test plans, protocols, and reports
• Plan and execute test method validation activities, including assessing accuracy, precision, and repeatability
• Ensure all testing and documentation aligns with Good Laboratory Practice (GLP) and Quality Management System (QMS) standards
• Support continuous improvement initiatives to enhance laboratory processes and testing efficiency
• Collaborate cross-functionally with engineering, quality, and manufacturing teams to resolve issues and improve product performance

• Bachelor's degree in Engineering, Life Sciences, or a related technical field (or equivalent technician experience with laboratory background)
• Minimum of 3 years of hands-on experience in test method validation within a laboratory environment
• Experience working with electrical and/or mechanical systems and performing related testing
• Proficiency in statistical analysis tools (e.g., Minitab or similar software)
• Hands-on experience with laboratory and testing equipment such as microscopes, multimeters, pressure sensors, and thermocouples
• Strong documentation skills with experience in GLP and QMS environments

• Experience in a regulated industry such as medical devices, pharmaceuticals, or biotechnology
• Familiarity with FDA regulations and industry standards
• Strong analytical and problem-solving skills with attention to detail
• Excellent written and verbal communication skills

• Onsite laboratory setting in Danvers, MA
• Hands-on work with testing equipment and engineering systems
• Collaborative, cross-functional team environment