Regulatory Affairs Specialist

  • Company: Adecco
  • Location: South Plainfield, New Jersey
  • Posted: November 25, 2016
  • Reference ID: 2126192266

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.
JOB REQUIREMENTS:

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 heena.verma@adeccona.com
If you have questions about the position please contact Heena Verma at 212-391-7000 or at heena.verma@adeccona.com.






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