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千代田区
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Assoc. Dir., Regulatory Affairs

MSD
千代田区
フルタイム
2日前

Job Description

POSITION OVERVIEW:

The Associate Director of the Regulatory Affairs (RA) is responsible for the overall management of regulatory affairs activities including pharmacovigilance work at RA department at PDRA division Animal Health in Japan. The position requires a combination of scientific knowledge, understanding of regulatory requirements, strategic thinking, and team leadership to ensure timely development of new products and regulatory affairs activities.

The individual will ensure that the RA team develops and successfully executes project plans for timely product registrations.  

The individual will motivate and encourage the RA Team to perform successfully and will mentor and coach team members to oversee their personal development in the organization.

The individual will closely communicate with members at the Product Development department to optimize the regulatory submission and get products approved.

Reporting lines:

PRIMARY ACTIVITIES:  

BACKGROUND REQUIREMENTS

Following leadership behaviors are expected

Education

Experience

Skills, Knowledge and Competencies

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:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Adaptability, Adaptability, Animal Husbandry, Change Management, Communication, Cross-Cultural Awareness, Cross-Team Coordination, Data Management, Employee Training Programs, FDA Regulations, Maintenance Processes, Management Process, Microsoft Office, Pharmacovigilance, Policy Implementation, Product Development, Product Registrations, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Compliance, Regulatory Labeling, Regulatory Management, Regulatory Operations, Regulatory Submissions, Software Office {+ 2 more}

 Preferred Skills:

Job Posting End Date:

06/30/2026

*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.

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