Job Description

Job Responsibilities:

Manage registered products and register new products within the team agreed timeline. Tasks Include but not limited to:

• Communicate with international RA team contactor
• Preparing registration dossiers and relative question
• Follow up registration procedure
• Make good relationship with key stakeholders
• Organize the registration evaluation meeting
• Get final registration permits
• Update related registration regulations

Job Requirements:

• Above 6 years working experience in Regulatory Affaris in pharma industry. Experience in Oncology/CDx/IVD is a plus.
• Profiency in both English and Chinese communication.

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
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.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

05/31/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.