This is an opportunity to register your interest in future Test Engineer roles within regulated manufacturing environments, positions that could involve validating critical components and systems throughout product development and manufacturing. Please note the content of this advert does not represent a live vacancy. About the opportunity Roles of this type may sit within quality assurance and validation teams at organizations advancing regulated products—such as medical devices, diagnostics, or life sciences equipment—where testing protocols and design validation are central to bringing safe, effective solutions to market. The work could involve designing and executing test plans, analyzing validation data, and collaborating across engineering and quality functions to ensure products meet design specifications and regulatory requirements. Typical role overview

Location:

Boston, Massachusetts, USA Type:

Contract •

Full-time Rate:

$560-$800 per day

Domain:

Regulated manufacturing • quality assurance and validation Experience level: 2-5 years in testing, validation or quality assurance What you would do Typical responsibilities could include: Designing and executing test protocols and validation studies according to design control and regulatory requirements Analyzing test data, documenting results and preparing validation reports for design and manufacturing files Collaborating with engineering and quality teams to troubleshoot failures and drive corrective actions Supporting design verification and validation activities throughout product development Maintaining detailed test documentation and ensuring traceability to design specifications Contributing to continuous improvement of testing procedures and quality management systems Participating in design reviews and providing input on testability and validation strategy What you could bring Most roles of this type require the following: Must-have 2-5 years' experience in test engineering, validation engineering, quality assurance or a related discipline Hands-on experience designing and executing validation protocols in a regulated manufacturing or product development environment Knowledge of design control, testing standards and quality management systems (QMS) Strong documentation and data analysis skills Bachelor's degree in Engineering, Life Sciences or a related field Authorization to work in the United States Nice-to-have ISTQB Certified Tester or ISTQB Advanced Tester certification Experience with CAD software or design documentation systems Familiarity with medical device regulations (FDA, ISO 13485) or equivalent standards Field application or manufacturing experience What roles of this type could offer Most roles of this type offer the following, dependent on the industry and seniority of the role: Hands-on involvement in validating products that could impact patient outcomes or safety Exposure to regulated product development and quality systems Opportunity to develop expertise in testing protocols, design standards and regulatory compliance Collaboration with cross-functional engineering and quality teams Contract flexibility and the potential for extension based on project needs Professional development in validation methodology and quality assurance practices About Specialist Staffing Group We are a specialized staffing and recruitment partner focused on engineering, life sciences and technical talent. Our mission is to connect skilled professionals with meaningful opportunities in regulated manufacturing, product development and quality assurance. We work with leading organizations to build high-performing teams that drive innovation and ensure product excellence. How to register interest If you are interested in being added to our database to be considered for future opportunities, registering is quick and easy. No cover letter required. We will be in touch when we are instructed on these roles to discuss the next step in your career. Please note that the content of this advert does not represent a live vacancy or any guarantee of future vacancies, and by responding to this advert you agree to us adding your details to our database for future opportunities.