Merck logo
默克药厂
Project Analyst - Regulatory Business Transformation

Project Analyst - Regulatory Business Transformation

发布于 41 分钟前

普通员工/个人贡献者

Bangalore, Karnataka, India
高级经验
全职员工
仅现场办公
硕士
合规
Kpi
Palantir
Regulatory Affairs
Sap
Stakeholder Management

AI 估算 · 25k–45k

海外跨国药企,法规与项目复合技能,班加罗尔中高薪水平,折合人民币约3-4万/月。

职位详情

关于这个职位

该职位是默克制药在印度班加罗尔的一个业务转型项目分析师角色,结合法规事务与项目管理两大职能,负责确保生命科学产品按时上市,并通过数据驱动的绩效管理优化流程

你将与全球团队协作,处理产品法规数据,监控KPI并推动项目交付

最低要求

自然科学或相关领域硕士学位

年以上法规事务和项目管理经验
有KPI监控、绩效分析和数据驱动的改进规划经验
熟练使用SAP、JIRA、Palantir和Microsoft 365
优秀的沟通能力和利益相关者管理能力
自驱力强,善于解决问题和批判性思维,具有协作精神,无需权威也能施加影响

工作职责

【法规事务(50%)】

与全球产品管理、法规和外部团队合作,确保产品准确、按时上市
收集、整合和验证产品成分、物理和法规数据,用于评估和危险特性分析
与内部处理团队合作,确保法规决策在整个产品生命周期中得到正确应用
【项目管理(50%)】
全权负责所分配项目的端到端交付,满足里程碑、时间表和利益相关者承诺
监控运营KPI,及早识别风险,并制定包含明确行动和负责人的改进计划
编写状态报告和高管汇报材料,将数据转化为可供领导层参考的可行见解
应用项目管理方法跟踪任务、管理风险,并协调跨职能团队工作

AI 洞察

优缺点分析

优点

  • Work for a global pharmaceutical leader with strong reputation in life sciences.
  • Gain dual expertise in regulatory affairs and project management, increasing career versatility.
  • International collaboration exposes you to diverse cultures and best practices.
  • Competitive compensation and benefits typical of large multinational corporations.
  • Balancing dual responsibilities requires excellent time management and prioritization skills.
  • Regulatory processes can be complex and changing, requiring continuous learning and adaptability.
  • Given the global nature, may need to coordinate across different time zones, impacting work-life balance.
  • This role suits candidates who enjoy structured project work, have strong attention to detail, and are comfortable navigating regulatory frameworks in a dynamic, multicultural environment.

缺点 / 挑战

暂无明显挑战项

角色解读

  • Progress to a senior regulatory transformation lead or program manager role within the organization.
  • Expand expertise in life science regulations and process optimization, enabling broader strategic impact.
  • Opportunity to move into leadership positions in regulatory operations or project delivery.
  • You manage regulatory submissions and product launch compliance data for the Life Science business.
  • You lead project delivery end-to-end, ensuring milestones, KPIs, and stakeholder expectations are met.
  • You analyze operational data and translate findings into executive-level insights and action plans.
  • You collaborate with cross-functional teams globally to align regulatory decisions across the product lifecycle.
  • Strong background in regulatory affairs and project management methodologies.
  • Data-driven mindset with hands-on experience in KPI monitoring and performance analysis.
  • Proficiency in SAP, JIRA, Palantir, and Microsoft 365 for data management and reporting.
  • Excellent communication and stakeholder management skills to influence without authority.

申请策略

  • Research Merck's life science division and recent product launches to show genuine interest.
  • Tailor your CV to mirror the dual nature of the role, using keywords like regulatory affairs, project management, KPI, and stakeholder management.
  • Highlight your experience in regulatory affairs, especially product launch activities.
  • Showcase successful project management examples with quantified results (e.g., on-time delivery, KPI improvements).
  • Emphasize proficiency in SAP, JIRA, Palantir, and analytical tools with specific use cases.
  • Demonstrate stakeholder management abilities through examples of influencing cross-functional teams.
  • Take project management certifications like PMP or PRINCE2 to strengthen your credentials.
  • Familiarize yourself with life science regulatory frameworks such as REACH or GHS if not already.

面试指南

  • Use the STAR method (Situation, Task, Action, Result) to structure responses, focusing on measurable outcomes.
  • For KPI questions, explain your process: identify metrics, track trends, use data to diagnose issues, and implement improvements.
  • For influence questions, demonstrate how you built relationships, understood others' perspectives, and aligned goals.
  • Can you describe a complex regulatory submission project you managed? How did you ensure timely completion?
  • How do you monitor project KPIs and decide when to escalate risks?
  • Tell me about a time you influenced stakeholders without formal authority.
  • How would you approach the lifecycle management of a product's regulatory data?
  • What experience do you have with SAP and JIRA in a regulatory or project management context?

职位点评

65
综合评分

Meaningful regulatory/project role at a global pharma leader, with decent compensation but unclear work-life balance.

从薪资福利、成长空间、工作节奏和岗位方向综合评估,方便横向比较。

更适合这类人
This role is ideal for candidates who value purposeful work in healthcare/life sciences and professional development over strict work-life balance.
表现最好
使命价值
相对薄弱
工作生活
薪资福利65
成长发展70
工作生活50
使命价值80

薪资福利

65中等

Compensation is competitive for India, and working for a global giant provides stability, but specific benefits are not disclosed in the JD.

薪资信号未披露(AI估算:25K-45K/月)

成长发展

70中等

The role offers exposure to regulatory affairs and project management, with excellent upskilling potential, though no explicit promotion path is mentioned.

技术前沿非技术岗(不适用)
技术栈SAP、JIRA、Palantir、Microsoft 365
成长机会develop and grow
业务类型ambiguous

工作生活

50较低

Work mode is not specified; likely office-based in Bangalore. No explicit work-life balance signals, and global collaboration may require flexible hours.

工作模式未明确
办公地点海外(不适用)
加班情况未提及(无法判断)

使命价值

80较高

The company explicitly mentions improving people's lives through healthcare and life science, giving the role a strong sense of purpose.

行业发展稳定成熟行业
社会影响正向社会影响力较高
使命信号enrich people's lives、caring for our rich mix of people, customers, patients
创新程度稳健跟随主流
Watch Jobs