We are ISO 9001 and ISO 13485, as well an FDA Registered Medical Device Manufacturer. We are currently seeking QA Regulatory Compliance Interns who are looking for hands on experience with a medical device manufacturer.
All internships are paid. Opportunities include but are not limited to:
- Research and Development Projects
- Non Conforming Materials
- Creation and modifications of SOP’s
- QC and testing of incoming materials and finished goods
- Surveillance Audits of our Quality System
- Maintenance of our Quality System
- CAPA Projects including general deviations, non-conforming products, re work instructions, and “how to’s” for technical teams
- Vendor Qualification, Quality Surveillance, Agreements and mitigation of non conforming materials and products
- Participation in regulatory audtics
- Technical File preparation and project management
- 510K Submission preparation and project management
Our technology and product range include:
- Sports Medicine
- Pain Control
- Rehabilitation
- Medical Aesthetics
- Skin Care
- Consumer