Additive Manufacturing; AM Technician
Listed on 2026-07-06
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Quality Assurance - QA/QC
Production QC/QA, Quality Engineering -
Manufacturing / Production
Production QC/QA, Quality Engineering
What You Can Expect
Passionate about Orthopedic Medical Device and 3D printing? Paragon 28 (Zimmer Biomet), a Foot and Ankle orthopedic medical device company, is hiring an Additive Manufacturing Technician for our Englewood, Colorado location. This position is 100% onsite in Englewood Colorado.
The Additive Manufacturing Technician plays a hands‑on role in bringing innovative medical devices to life. This position is responsible for setting up, operating, and performing preventive maintenance on SLS additive manufacturing machines, processing equipment, and related processes within an ISO 13485 manufacturing environment. At Paragon 28, the technician will manufacture, inspect, and help qualify 3D‑printed parts that support the production of high‑quality medical devices.
This role is involved throughout the production process, from receiving files and preparing builds to scheduling, part finishing, and final inspection. The technician will also help maintain reliable production by performing routine process maintenance and partnering with engineering to support new product qualifications. In addition, this position provides important documentation support to keep the lab organized and compliant, including maintaining accurate records for incoming products and process updates.
This is an excellent opportunity for a detail‑oriented, motivated individual who is eager to learn and grow in the field of additive manufacturing. The ideal candidate enjoys hands‑on technical work, takes initiative, and values accuracy in both production and documentation. Success in this role requires strong attention to detail, the ability to work independently, and a commitment to supporting quality systems in a regulated environment.
HowYou'll Create Impact Essential Responsibilities and Duties
- Set up, operate, and maintain additive manufacturing (AM) machines, post-processing equipment, and tensile testing machine.
- Monitor and record operational information, including functional issues, material consumption rates, and build completion dates.
- Follow work orders, procedures, specifications, and test instructions.
- Utilize various quality control gauges and measurement tools to inspect and measure parts.
- Review work instructions for additional information and special requirements.
- Ensure compliance with all Quality Management Systems, including adherence to good documentation practices (GDP).
- Assist with creating, reviewing, and maintaining process documentation in compliance with ISO 13485 and internal Quality Management System (QMS) requirements.
- Support validation activities, including test method validation and process qualification documentation.
- Identify and troubleshoot machine and manufacturing issues.
- Maintain thorough and accurate records of manufacturing activities.
- Contribute to process improvements by identifying inefficiencies and proposing solutions in collaboration with engineering and quality teams.
- Perform other assigned duties as required.
- Currently pursuing or completed an Associate degree in engineering sciences or a related technical discipline. (Availability during standard on‑site working hours in the lab is required).
- Strong time management, prioritization skills, and attention to detail.
- Basic understanding of Additive Manufacturing technologies.
- Proficiency with manufacturing equipment and quality inspection tools.
- Ability to work independently and complete tasks with minimal supervision.
- Experience with basic shop tools and hand tools.
- Proficiency in Microsoft Office applications, including Outlook, Excel, and Word.
- Basic computer skills required, including the ability to download files, organize files, and upload documents to SharePoint or similar platforms.
- Strong problem‑solving skills and the ability to adapt to evolving manufacturing and quality requirements.
- Ability to take initiative and seek guidance when needed to ensure manufacturing and documentation processes meet compliance standards.
- Excellent verbal and written communication skills.
- Experience working in an ISO 13485‑regulated environment.
- Familiarity with Additive Manufacturing processes and…
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