Regulatory Affairs Consultant - CMC biologics (home or office based)
Parexel(5 months ago)
About this role
Parexel is seeking a Regulatory Affairs Consultant to support a client-dedicated project focused on worldwide post-approval regulatory activities for biological products, with an emphasis on CMC. The role operates across various European locations and can be office- or home-based, contributing to the ongoing maintenance and evolution of approved products in global markets.
Required Skills
- Regulatory Affairs
- CMC
- Submission Strategy
- Post-Approval Submissions
- Variations
- Renewals
- Change Control
- Regulatory Writing
- Risk Mitigation
- Project Management
+5 more
Qualifications
- University Degree (Life Sciences)
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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