4 validation engineer ii jobs found

For further inquiries regarding the following opportunity, please contact our Talent Specialist, Gopalakrishnan at (224) 369-4243 Title: Contract Mechanical Engineer II - Controls Experience Location: Onsite at Newton, NC Duration: 12 Months Hours: 40 hrs a week / 8 hrs a day 8 AM - 5 PM Monday - Friday and occasional OT Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered. Description: Position Overview We are seeking a Contract Mechanical Engineer II with manufacturing automation and controls experience to support the design, build, integration, and continuous improvement of automated manufacturing equipment and production systems. This role is ideal for an engineer with a solid background in mechanical design who has worked closely with controls, electrical, and manufacturing teams on automation equipment, machine upgrades, and process improvement initiatives. The engineer will contribute to projects...

The Transfer Engineer I-II plays a key role in supporting and leading the transfer of interventional and transcatheter medical devices from development into production. This position contributes to Aptyx's end-to-end solutions for Class II and III medical devices, including implants, catheters, and other disposable products. This role spans early-career to mid-level engineering capability, with increasing responsibility for process development, validation, equipment implementation, and customer engagement. The Transfer Engineer will work cross-functionally with Operations, Quality, Supply Chain, and customers to deliver robust, scalable, and cost-effective manufacturing processes. Duties and Responsibilities Quality System & Compliance Follow the Aptyx Quality System and all applicable SOPs within the Training Matrix. Ensure compliance with medical device regulations and internal validation standards. Process Development & Manufacturing Transfer Support...

The Engineer II - Senior R&D Engineer performs design engineering and technical leadership within the Development organization, supporting the development of Class II and Class III medical devices across multiple therapeutic areas including cardiology, neurology, and urology. This role supports or leads cross-functional project teams from concept through commercialization, ensuring delivery of customer requirements for quality, cost, and timeline objectives. The engineer contributes to or leads technical execution, communicates project status, and ensures engineering deliverables align with regulatory and quality system requirements. Engineer II-level employees operate with moderate supervision, while Senior Engineers lead technical execution, mentor team members, and drive project outcomes with minimal oversight. Key Responsibilities Product Development & Engineering Execution Follow Aptyx Quality System, including all applicable SOPs and training requirements...

The R&D Engineer II performs design engineering functions in support of medical device product development programs across multiple therapeutic areas including cardiology, neurology, and urology. This role contributes to projects from concept through commercialization, ensuring deliverables meet customer requirements for quality, cost, and schedule performance. The Engineer II works with moderate independence to execute engineering tasks, support project deliverables assigned by the Project Manager, and communicate technical status updates to cross-functional teams. Updates may include technical feasibility, schedule impact, budget considerations, and risk to project objectives. This role also supports development of engineering processes, manufacturing readiness, and continuous improvement of product and design solutions within a regulated environment. Key Responsibilities Product Design & Development Follow the Aptyx Quality System, including all applicable SOPs...