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What does SAGE Therapeutics do?

Sage Therapeutics, Inc. is a biopharmaceutical company that develops and commercializes brain health medicines. ...

What does a regulatory affairs specialist Medtech do?

Minimum of 15 years’ experience, with exposure to business functions such as compliance, legal, regulatory affairs, governmental affairs, and/or finance. The Regulatory Affairs Specialist MedTech will be a member of the local regulatory affairs department within Johnson & Johnson Medical, with responsibility to… ...

What does a regulatory affairs specialist do?

Coordinating with regulatory authorities, such as the Health Sciences Authority (HSA) in Singapore, to ensure timely approval and compliance with regulatory… More... Support regulatory submissions in our regional markets. The point of contact with the Regulators, the Regulatory Affairs Specialist provides regulatory support… More... ...

What can I do with a degree in Drug Safety & Regulatory Affairs?

This entry-level position is ideal for recent graduates with a keen interest in drug safety and regulatory affairs. Total work: 1 year (Preferred). More... Liaising and negotiating with regulatory authorities. Keeping up to date with changes in regulatory legislation and guidelines. Job Types: Full-time, Fresher. More... ...

What skills do you need to be a regulatory affairs manager?

Assist regulatory affairs teams in associated companies. Hands-on experience in regulatory affairs. Basic knowledge of regulatory affairs and pharmaceutical… More... Experience- Minimum 3 years in regulatory affairs for ROW market (Rest of the world). Preparing dossiers as per country specific guidelines. More... ...