Job Description

R&D PROCESS ENGINEER

Reports to: Senior Manager, R&D and Process Engineering

ABOUT SMILE INNOVATIONS GROUP

Smile Innovations Group is national organization focused on the consolidation of dental labs and development of dental products and services. Our management team has a long history and experience in the dental and financial industries providing a wide range of knowledge. Our team has been involved in a long list of M&A deals and has experience in the operational management of large-scale businesses.

Job Summary

We are seeking a skilled Process Engineer with hands-on experience in equipment and process validation, specifically in IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification). The successful candidate will be responsible for ensuring that equipment, systems, and manufacturing processes are installed, tested, and operate in compliance with regulatory and company standards. The role will evolve into a key contributor within our R&D and Process Engineering group, helping drive innovation and continuous improvement in digital manufacturing.

Key Responsibilities

Lead and execute IQ/OQ/PQ protocols for SLM machines and related systems. Develop detailed validation protocols and reports in compliance with GMP, ISO, and internal SOPs. Collaborate with cross-functional teams (Quality, Manufacturing, Maintenance, R&D) to ensure coordinated validation execution. Troubleshoot issues during validation and perform root cause analysis and resolution. Support project timelines by executing validation activities efficiently and accurately. Explore and evaluate new technologies in digital dentistry (e.g., 3D printers, milling machines, materials, software). Drive workflow innovation, process automation, and improved clinical outcomes through applied engineering. Translate R&D outputs into scalable processes, ensuring proper handoff and implementation across production labs. Stay current on emerging trends and technologies in dental manufacturing.

Requirements

Bachelor's degree in Engineering (Mechanical, Chemical, Biomedical, or related field). Minimum of 3 years' experience in validation engineering, with a focus on IQ/OQ/PQ in regulated industries (medical device, biotech, or pharma). Solid knowledge of Good Manufacturing Practices (GMP), ISO 9001, and risk-based validation approaches. Strong technical writing, documentation, and communication skills. Proven ability to manage multiple projects and work independently.

Preferred Qualifications

Experience with R&D, digital manufacturing, and dental lab processes. Familiarity with digital dental manufacturing tools such as SLM printers, SLA/DLP 3D printers, and milling systems. * Experience with Lean Six Sigma and continuous improvement initiatives.