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Merck & Co. · CHN - Beijing - Beijing

# Asso. Manager, Regulatory Affairs (Animal Health)

CHN - Beijing - Beijing Full-time Manager or lead Legal & Compliance 

Listed on Merck & Co.’s official careers site. Posted October 13, 2026. Check that it is still open and apply there.
[Apply on Merck & Co.’s careers site →](https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Beijing---Beijing-Wangjing-Park/Asso-Manager--Regulatory-Affairs--Animal-Health-_R419707-2)

[OpenNash Jobs](https://jobs.opennash.com/) / [Merck & Co.](https://jobs.opennash.com/companies/merck-co/) / Asso. Manager, Regulatory Affairs (Animal Health)

## Job description

Job Description 职位名称 / Job Title 法规事务助理经理（Associate Manager, Regulatory Affairs） 岗位使命 / Mission 通过高质量、高效率的产品生命周期管理与合规运营，确保已上市兽用疫苗产品持续合规、稳定供应。 Ensure the ongoing compliance and reliable supply of marketed veterinary vaccines through high-quality lifecycle management and regulatory compliance.

### 主要职责 / Key Responsibilities 产品注册与生命周期管理

依据中国法规要求完成注册、续展、变更等申报工作，跟进审评进展，保障产品持续合规和稳定供应。

### Registration and lifecycle management

Prepare and maintain regulatory submissions, including registrations, renewals, and variations, in accordance with China regulations; track review progress and ensure ongoing compliance and reliable product supply.

### 法规指导

为研发与商业化提供清晰、及时、可落地的法规建议与路径。

### Regulatory guidance

Provide clear, timely, actionable regulatory advice for R&D and commercialization.

### 法规与标准管理

跟踪并评估法规、兽药典标准及技术指导原则变化，推动内部实施，确保产品持续符合监管要求。

### Regulatory and standards management

Monitor and assess changes in regulations, pharmacopoeia standards, and technical guidelines; drive internal implementation and ensure continued compliance with regulatory requirements.

### 合规管理

监测法规变化，维护产品全生命周期合规，推动必要的内部改进。

### Compliance oversight

Monitor regulatory changes, ensure lifecycle compliance, drive essential internal improvements.

### 任职要求 / Requirements 学历与背景

预防兽医、生物科学或相关专业本科及以上学历；至少6年法规事务经验；熟悉中国兽药法规、审评实践、法规标准体系及技术指导原则，具备相关要求解读与实施经验。

### Education & background

Bachelor's degree or above in Preventive Veterinary Medicine, Biosciences, or a related field; 6+ years of regulatory affairs experience; strong knowledge of China veterinary drug regulations, review practices, regulatory standards, and technical guidelines, with demonstrated experience in their interpretation and implementation.

### 关键能力（对齐岗位意义

及时拿证/解决问题）/ Core capabilities (aligned with role purpose: timely approvals/problem-solving): 清晰度：能清晰定义问题与路径，提供明确法规指导，确保沟通高效、信息无歧义。

### Clarity

Ability to define issues and pathways clearly, provide precise regulatory guidance, and communicate without ambiguity.

### 及时交付

时间敏感与按期交付，首次准确（First-time-right），在压力下保持质量与速度。

### No delay

Time sensitivity and on-time delivery, first-time-right quality, maintaining speed and quality under pressure.

### 关键问题处理

快速识别关键点，完成结构化分析并提出可执行建议，推动闭环解决与经验沉淀。

### Critical issue handling

Rapid identification, structured analysis, actionable recommendations, and driving closure with learnings captured.

### 风险判断与承担

准确解读法规与监管期望，评估选项与边界，适时升级并高质量落地。

### Risk judgment and ownership

Accurate interpretation of regulations, assessment of options and boundaries, timely escalation, and high-quality execution.

### 战略思维

在商业与技术框架下做出务实选择，平衡资源与合规风险。

### Strategic thinking (1-year horizon)

Pragmatic choices within business and technical frames, balancing resources and compliance risk.

### 团队协作与影响

稳定交付，支持团队成员，跨部门协同提升整体效率；具备职权或非职权领导力与谈判影响力。

### Collaboration and influence

Reliable delivery, support teammates, cross-functional coordination to lift efficiency; authority or informal leadership and negotiation influence.

### 基础技能与素质 / Foundational skills and attributes

优秀的沟通与组织能力；强逻辑与数据分析能力；细节导向与质量意识。 Excellent communication and organization; strong logic and data analysis; detail orientation and quality mindset. 熟悉新产品开发流程与质量管理体系；具备日常法规决策与假设管理能力。 Familiarity with new product development processes and QMS; capable of day-to-day regulatory decision-making and hypothesis management. 自我驱动、有担当，能在最少监督下高效工作。 Self-driven with ownership; effective under minimal supervision.

### Additional location(s) Compensation Information

Required Skills: Drug Regulatory Affairs, Government Regulation, Influencing Skills, Influencing Without Authority, Policy Compliance, Regulatory Affairs Management, Regulatory Compliance, Regulatory Operations Preferred Skills: 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: 10% Flexible Work Arrangements: Not Applicable Shift: Not Indicated Valid Driving License: No Hazardous Material(s): n/a Job Posting End Date: 12/31/2026 *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.

## At a glance
- Posted by the employer: Oct 13, 2026
- First seen by OpenNash: Oct 18, 2026
- Last checked: Oct 18, 2026
- Listed for: 5 days
- Location: CHN - Beijing - Beijing
- Employment type: Full-time[Apply on Merck & Co.’s careers site →](https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Beijing---Beijing-Wangjing-Park/Asso-Manager--Regulatory-Affairs--Animal-Health-_R419707-2)

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