6386 - Technical Specialist / Data Analyst
Tasks
- Coordinate implementation of changes across manufacturing sites
- Coordinate post market surveillance reports
- Coordinate with cross functional teams to ensure supply continuity
- Create and manage design control documentation
- Generate annual risk summaries
- Initiate route and close change records
- Maintain risk management files for medical devices
- Manage combination product change control records
- Support complaint investigations and documentation
- Update risk management files
Perks/Benefits
- 401k retirement plan
- Disability insurance
- Medical/Dental/Vision insurance
- Paid parental leave
- Paid time off
- Tuition reimbursement
Skills/Tech-stack
CGMP | Change Control | Design Controls | Market surveillance | Medical Device | Medical device regulation | Pharmaceutical Regulation | Post-Market Surveillance | Project Management | Quality management | Risk Management | Veeva Vault
Education
Roles
Regions
Countries
States
Cities
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