Document Control Specialist
hace 1 mes
At Corza Medical, we are seeking a highly skilled Document Control Specialist to join our team. As a key member of our regulatory compliance department, you will be responsible for ensuring that all documents and product specifications are processed and maintained in accordance with good manufacturing practices, ISO 13485, CFR 21 Part 820 requirements, and other applicable standards and regulations.
Key Responsibilities:- Supervise activities within the Document Control area.
- Process product changes and new product introduction in Veeva & D365 systems.
- Process documents and product specifications in Veeva.
- Scan and control files of product specifications and documents.
- Ensure Document Control, Change Request, and DHR Control processes are properly followed.
- Maintain revision of documents and ensure all procedures are updated as needed.
- Support internal & external audits.
- Assist users in Veeva & D365.
- Develop procedures, processes, and change requirements for applicable areas in Document Control.
- Assign and control temporary deviations.
- 2-5 years of experience.
- Advanced English preferred.
- Customer First.
- Accountability.
- Integrity.
- Inspired.
- One Global Team.
We are an Equal Opportunity Employer: Corza Medical evaluates qualified applicants without regard to race, color, marital status, religion, sex, sexual orientation, gender identity, age, national origin, physical or mental disability, veteran status, or other protected characteristics.
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