Come join our revolutionary and growing Medical Device client that is looking for an experienced Document Control Specialist!
Responsibilities:
- Develop & implement robust record retention policies & electronic file systems.
- Ensure flawless documentation, meeting regulatory & internal standards.
- Streamline document retrieval, making knowledge readily accessible for all.
- Oversee document change orders, adhering to established processes & training colleagues.
- Manage Design History Files, key company directories, & Microsoft Access databases.
Qualifications:
- Bachelor's degree and experience in the Medical Device industry
- Experience with whole product lifecycle management (PLM)
- Working knowledge of QMS, CAD files, Adobe, label software, etc.
Please do not hesitate to apply!
