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Director, GRA CMC Pharmaceuticals, Oligonucleotides
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$165,200 a year
Full-time
- Join Takeda as a Director, GRA CMC Pharmaceuticals, Oligonucleotides where you will lead the GRA CMC Pharmaceuticals regulatory team in the development and implementation of global CMC regulatory strategies during development commercialization and post approval LCM stages.
- Establish collaboration with Global CMC teams and leadership through networks and enable CMC regulatory teams success in meeting goals/objectives.
- As part of the GRA CMC Pharmaceuticals, Oligonucleotides team, you will report to the Executive Director and Head, CMC Regulatory Affairs, Pharmaceuticals.
- In conjunction with members of the team, develop high quality clinical, commercialization and LCM submissions, using proactive regulatory CMC strategies and submit them as planned.
- Build and manage relationships through active partnering with key internal (GRA, GRA CMC, Pharmaceutical Sciences, GMS, GQ etc.)
Expired 22 days agoInactive Job
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