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Asso. Manager, Regulatory Affairs; Animal Health

Job in Belfast, County Antrim, BT1, Northern Ireland, UK
Listing for: MSD
Full Time position
Listed on 2026-10-16
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 70000 - 100000 GBP Yearly GBP 70000.00 100000.00 YEAR
Job Description & How to Apply Below
Job Title

法规事务助理经理(Associate Manager, Regulatory Affairs)

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.

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.
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 and 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, 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.
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…
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