Adecco Medical & Science has a current job opportunity for a Regulatory Affairs Specialist in South Plainfield, NJ. In this direct-hire role, you will provide strategic and operational direction and oversee the regulatory process. As a Regulatory Affairs liaison, you will contribute to the development and implementation of regulatory strategy, translate requirements into work plans, author SOPs, and manage submissions.
MS or PhD in Pharmacy, Chemistry, Chemical Engineering, or related field
3+ years' experience in pharmaceutical regulatory affairs
Experience with ANDA, NDA, 510K, CMC, CTAs, PSUR, International regulations, etc.
5-7 years of product development experience
To be considered, please use the "apply now" button or submit your resume directly to email@example.com
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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