默克药厂
Expert Manufacturing & EMEA Applications
Expert Manufacturing & EMEA Applications
发布于 大约 22 小时前普通员工/个人贡献者
Mollet del Valles, Barcelona, Spain
专家级经验
全职员工
仅现场办公
本科
项目管理
ITIL
英语
西班牙语
合规
SCADA
MES
质量管理
GxP
LIMS
AI 估算 · 48k–64k
Expert级别在西班牙制药IT领域，结合公司规模和行业，月薪约6000-8000欧元，换算人民币后给出
职位详情
关于这个职位
作为一名Expert Manufacturing & EMEA Applications，您将负责默克在西班牙及欧洲的制造、质量和运营技术领域的IT项目与服务
您需要管理GxP相关系统（如LIMS、MES、SCADA）的合规性与安全性，与本地用户和利益相关者协作，并领导供应商和承包商以确保业务连续性
该职位适合具有5年以上工业IT经验、熟悉制药合规要求且能独立工作的专业人士
最低要求
You hold a Bachelor degree in computer science, engineering or a natural science degree combined with strong IT knowledge. Experienced delivery manager with a minimum of 5 years relevant practice and exposure to an industrial IT environment with clear responsibilities, ideally for manufacturing, supply chain or quality systems. Self-motivated, highly engaged and autonomous individual with a strong ownership and service attitude. Team player who is used to work remotely in an international organization. Thoroughly familiar with current Quality & GxP IT/OT compliance trends for manufacturing & quality capabilities (e.g. LIMS, MES, LABs, SCADA, etc.) and underlying technology. Broad IT infrastructure knowledge (i.e. OS, DB, system hardening, etc.). Solid presentation and communication skills. Excellent command of written and spoken English.
工作职责
Deliver IT projects and services for business applications in the Manufacturing, Quality and Operations Technology domain. Support IT applications including quality and shop floor systems in collaboration with local end-users and business stakeholders. In charge of a number of ITIL defined processes such as service requests, change management, disaster recovery, life cycle, incident and problem management. Manage external suppliers and contractors to secure project support and business continuity according to service level agreements. Drive the execution of related IT project roadmaps in cooperation with project teams. Define the technical design of IT solutions together with Solution Architects. Ensure proper documentation of all activities performed in projects and during service management (e.g. qualification documents, work instructions, change requests, vulnerability management, etc.). Act as Qualification Owner, accountable for all compliance aspects of the portfolio of GxP relevant systems in Spain and other European countries, including security aspects.
优先资格
Solid foundation in IT service management methodology (preferably ITIL certification). Business fluent Spanish and French is a strong plus.
AI 洞察
优缺点分析
优点
- Global exposure and responsibility across Europe in a top-tier pharmaceutical company.
- High demand for GxP compliance expertise, offering strong job security and niche skills.
- Opportunity to work with cutting-edge manufacturing IT systems and influence quality processes.
- Autonomous role with ownership over critical systems, enabling professional growth.
- High regulatory pressure and strict compliance requirements can lead to meticulous documentation work.
- Need to manage multiple stakeholders and external vendors across different countries, requiring strong coordination.
- The role is based on-site in a manufacturing plant, limiting location flexibility.
- This role is ideal for experienced IT professionals who enjoy a structured, compliance-driven environment and want to make a direct impact on pharmaceutical manufacturing quality.
缺点 / 挑战
暂无明显挑战项
角色解读
- Move into senior expert roles or solution architect positions within the pharmaceutical IT domain.
- Transition to global IT leadership positions managing larger portfolios or regional teams.
- Specialize further in regulatory compliance or advanced manufacturing technologies (Industry 4.0).
- Lead IT projects for manufacturing and quality systems, ensuring compliance with GxP regulations.
- Manage service processes like incident, change, and problem management using ITIL framework.
- Act as Qualification Owner for GxP systems across Spain and Europe, handling audits and security.
- Collaborate with local users, global teams, and external vendors to deliver business solutions.
- Deep understanding of GxP compliance and relevant systems (LIMS, MES, SCADA).
- Hands-on IT infrastructure knowledge (OS, databases, system hardening).
- Strong project and vendor management skills, with ITIL certification preferred.
- Excellent communication in English
- Spanish and French are strong pluses.
申请策略
- Research Merck's commitment to innovation and sustainability, and align your motivation with their mission.
- Prepare examples that demonstrate ownership and problem-solving in a regulated environment.
- Emphasize experience with GxP systems (LIMS, MES, SCADA) and regulatory audits.
- Showcase ITIL process management and project delivery examples with quantifiable results.
- Highlight vendor management and cross-cultural collaboration in international settings.
- Include any language skills, especially Spanish or French, and IT certifications.
- Consider obtaining ITIL certification if not already held.
- Familiarize yourself with European pharmaceutical regulations and GxP documentation standards.
面试指南
- Use STAR method: Situation, Task, Action, Result, emphasizing compliance and collaboration.
- Demonstrate knowledge of ITIL processes and how they apply to GxP environments.
- Show ability to balance technical solutions with regulatory constraints.
- How do you ensure compliance with GxP regulations in an IT project?
- Describe a time you managed a critical incident in a manufacturing IT environment.
- How do you handle conflicts between business needs and regulatory requirements?
- Explain your experience with supplier and vendor management in a global context.
- What is your approach to documenting change requests and managing qualification documents?
匹配度报告
64
综合匹配度
Stable pharma giant, strong purpose, mature tech stack, limited flexibility.
适合人群
This role is best suited for candidates who prioritize meaningful work with social impact and stability over flexibility and lifestyle perks.
最强匹配
使命价值匹配
最弱匹配
工作生活匹配
薪资福利70
成长发展60
工作生活50
使命价值75
薪资福利匹配
70中等
The position offers competitive compensation typical for a multinational pharmaceutical company in Spain, but specific salary details are not disclosed. Benefits are not explicitly mentioned, but large corporates usually provide standard packages.
薪资信号未披露（AI估算：48K-64K/月）
成长发展匹配
60中等
The role focuses on maintaining and complying with existing systems (LIMS, MES, SCADA) rather than innovating with cutting-edge technology. However, exposure to international projects and potential for advancement within the company exist.
技术前沿传统/成熟技术
技术栈ITIL、GxP、LIMS、MES、SCADA
业务类型cost_center
工作生活匹配
50较低
The role requires on-site presence at a manufacturing plant in Mollet del Valles, limiting flexibility. No explicit WLB signals are provided, and remote work is only mentioned for international collaboration, not for the role itself.
工作模式仅现场办公
办公地点工厂/生产基地
加班情况未提及（无法判断）
使命价值匹配
75中等
Working for Merck, a global leader in healthcare and life sciences, provides a strong sense of purpose in improving people's lives. The role directly impacts quality and compliance in manufacturing, ensuring patient safety.
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
创新程度稳健跟随主流
Watch Jobs