Adecco Medical & Science has a current job opportunity for a Manager of Regulatory Affairs in South Plainfield, NJ. This role will provide strategic and operational direction and oversight to regulatory projects relating to product development, registration, etc. This role will oversee the regulatory approval process and handle all interactions with regulatory authorities.
MS or PhD (Chemistry or related/scientific field)
3+ years in pharmaceutical regulatory affairs
5-10 years in pharmaceutical product development
Experience authoring/reviewing SOPs
Manage all regulatory submissions
Experience with US and International filing regulations
If you're interested in this role, click "apply now" and submit your resume.
If you have questions about the position please contact Heena Verma at 212-391-7000 or at firstname.lastname@example.org.
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