Associate Specialist, Documentation
Edwards Lifesciences(1 month ago)
About this role
A Quality Assurance team member supporting medical device product development by ensuring documentation integrity and regulatory compliance. The role contributes to maintaining high standards of safety and integrity across the product lifecycle and collaborates with cross-functional teams to influence decision-making. Work helps optimize development processes to deliver safe, effective technologies for patients.
Required Skills
- Document Control
- Records Management
- Archiving
- Audit Support
- Data Entry
- CAPA
- PDM
- MS Office
- Communication
- Problem Solving
+1 more
Qualifications
- Bachelor's Degree in Related Field
- Diploma in Related Field
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