Medical device cleanroom assembly

Built by clinicians, biomed engineers, and regulatory pros.

Mission

Make dental device purchasing easier to inspect, easier to repeat, and easier to explain when a clinic, DSO, or distributor needs documentation before it can act.

Vision

By 2030, every Zimmer Biomet routed dental request will have a clean spec trail: product family, UDI reference, IFU path, and service owner in one packet.

Patient-First Engineering

Risk thinking starts with the procedure, not the spreadsheet.

QMS Discipline

ISO 13485 language is treated as daily work, not decorative copy.

Clinician Co-design

Oral surgeons and restorative teams shape how kits and documents are grouped.

Regulatory as a Skill

RA questions are handled early so quotes do not stall at final review.

Service Culture

Support staff learn how ordering choices affect the operatory and back office.

Inclusive Hiring

Biomed, dental assistant, supply chain, and QA backgrounds are valued together.

Clinical engineer at dental planning console
Regulatory affairs team in lab coats
Field service engineer servicing dental equipment
Cleanroom assembly station
Customer clinical training session
R&D whiteboard session

Open roles

RA Specialist · Biomed FSE · Dental Clinical Application Specialist · Supply Documentation Lead · Sterile Packaging Coordinator

Talk to the Team