Position Overview
At Advanced Sterilization Products, we're seeking a motivated and skilled Technician Specialist to join our team. In this critical role, you'll support and maintain advanced production equipment and automation systems for manufacturing life-saving medical devices. This position offers the opportunity to work with cutting-edge technology, contributing to the seamless operation and optimization of processes such as mixing, dispensing, and packaging biochemical components.
Primary Responsibilities
Troubleshoot, maintain, and upgrade manufacturing equipment, including automated assembly, liquid dispensing, labeling, and welding systems. Perform preventive maintenance and ensure timely documentation of activities. Research and procure parts and components to maximize equipment efficiency. Assist with engineering validations, verifications, and test protocols. Manage the manufacturing engineering lab and maintain spare parts inventory. Create and update manufacturing documentation via Change Orders. Provide technical expertise for equipment failure analysis and process improvements utilizing methodologies like Lean/Six Sigma, DFM, and SPC. Address technical challenges in daily manufacturing operations and recommend innovative solutions. Support technology transfers to external or international facilities as needed. Ensure compliance with regulatory standards such as GMP and ISO 13485. Perform additional duties, including occasional after-hours and weekend support, as required.Qualifications
Education
Associate degree in Electrical or Mechanical Engineering (preferred) or equivalent experience.Experience
Minimum 3 years of experience troubleshooting and maintaining automated equipment. At least 5 years in a manufacturing environment (medical device experience preferred). Expertise in robotics, semi-/fully automated systems, and HMIs is highly desirable.Skills and Knowledge
Advanced troubleshooting skills for electro-mechanical systems. Proficiency in pneumatics, fluid power, electrical and mechanical hardware, and schematics. Familiarity with PLCs, I/Os, vision systems, servo motors, and robotics. Skilled in CAD software (e.g., SolidWorks) and Microsoft applications. Strong verbal and written communication skills for effective collaboration across teams. Knowledge of ISO 13485, GMP, and FDA-regulated environments (preferred).Preferred Skills
Experience with process and equipment validation in a regulated industry. Familiarity with controlled environments and gowning protocols.Work Environment and Physical Requirements
Standing: Up to 60% Sitting: Up to 90% Walking: 10-20% Requires compliance with controlled environment protocols, including gowning.This role primarily focuses on 1st and 2nd shift work, with opportunities to showcase flexibility through occasional after-hours or weekend support as needed.
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Fortive Corporation Overview
Fortive’s essential technology makes the world stronger, safer, and smarter. We accelerate transformation across a broad range of applications including environmental, health and safety compliance, industrial condition monitoring, next-generation product design, and healthcare safety solutions.
We are a global industrial technology innovator with a startup spirit. Our forward-looking companies lead the way in software-powered workflow solutions, data-driven intelligence, AI-powered automation, and other disruptive technologies. We’re a force for progress, working alongside our customers and partners to solve challenges on a global scale, from workplace safety in the most demanding conditions to groundbreaking sustainability solutions.
We are a diverse team 18,000 strong, united by a dynamic, inclusive culture and energized by limitless learning and growth. We use the proven Fortive Business System (FBS) to accelerate our positive impact.
At Fortive, we believe in you. We believe in your potential—your ability to learn, grow, and make a difference.
At Fortive, we believe in us. We believe in the power of people working together to solve problems no one could solve alone.