Manager, Regulatory Affairs

Job Description

Position Overview

Independently manage projects of pipeline products and registered products, include but not limit to CTA, NDA, Renewal, Variations and related regulatory agency interactions. Achieve regulatory milestones within company determined timeline.

• Communicate with global RA and other stakeholders
• Preparing registration dossiers and responses to questions from CDE and other related agencies
• Follow up registration procedure
• Make good relationship with officials/reviewers
• Organize the preparation for CDE interactions (Pre-IND and Pre-NDA, etc.), include written consultation and panel meeting
• Get final registration permits
• Get related registration regulations knowledge and utilize in daily works
• Support manager to provide RA input on the strategic planning for all responsible products

Requirements

• At least 8 years working experience in pharma Industry
• Over 6 years’ experience in RA field. Experience with ophthalmology products is preferred
• Bachelor and above in medicine, pharmacy or related disciplines
• Good computer skill in EXCEL, POWERPOINT and WORD
• Good interpersonal communication skill
• Good English skills both in spoken and written

Additional location(s) Compensation Information:

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Current Contingent Workers apply HERE

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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

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