Job Description

Responsibilities:

• Work closely with Global colleagues to prepare dossiers and documents for product registration in China. Provide guidance and regulations required by the Chinese authorities for the documentation preparations. Independently undertake the project.
• Work closely with internal colleagues in China to ensure that product registration in China is valuable and meets the requirements and timelines.
• Keep in touch with the Chinese authorities and agencies, such as the MOA and the IVDC, to track the registration process. If needed, work with Global RA to prepare the answers to the questions.
• Interface and collaborate with the company's distributors and product importers in preparation and providing necessary documents and test results for sample and product import, and product marketing.
• Assist the supervisor in problem solving, preparation of study contracts, and external services.

Requirements:

• MS degree, Prevention Veterinary Medicine or equivalent;
• 7-8 years of direct regulatory affairs experience in veterinary products, R&D, QC, QA, CA , technical support, veterinary production, preferred experience in veterinary registration for a foreign company. Especially registering one product or leaded one R&D project is much better;
• Professional and scientific interface established within both professional societies and animal health authorities;
• Fluent oral English

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:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Adaptability, Adaptability, Audits Compliance, Business, Detail-Oriented, Doing Business in China, Drug Regulatory Affairs, Employee Training Programs, Global Communications, Management Process, Marketing, Pharmaceutical Regulatory Affairs, Pharmacovigilance, Process Improvements, Product Marketing, Product Registrations, Project Management, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Compliance, Regulatory Management, Regulatory Operations, Regulatory Strategy Development, Regulatory Submissions, Veterinary Epidemiology {+ 2 more}

Preferred Skills:

Job Posting End Date:

09/30/2025

*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.