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Validation Specialist (MDM)

Boehringer Ingelheim
Wrocław, województwo dolnośląskie
Full time
3 tygodnie temu

The position


Joining our company, you will gather an overview of the GBS Enabling Services Organization with a particular focus on the tasks and responsibilities from Validation Management. You will work in a globally operating team that designs, builds and continuously improves Boehringer Ingelheim’s global Processes, using agile principles, methods and tools on a daily basis.


You will be qualified to contribute to a cross-functional team, and as a Validation Specialist you will be able to coordinate the activities around change requests, performing impact analysis, reviewing, and approving documents and ensuring a validated state of the system.


Tasks & responsibilities


  • Based on your expertise in Computer System Validation you ensure that changes are managed according to our validation rules in close cooperation with local experts in our GBS user community as well as cloud application suppliers.
  • Acting as a Validation Specialist, you support our daily operation of processes and applications.
  • You ensure that our processes and systems are always compliant and in a validated state.
  • Furthermore, you manage the execution and documentation of testing activities.
  • You are familiar with Agile methods and tools, participating to projects driven with this methodology.
  • You are familiar with working in projects and being measured against Key Performance Indicators (KPIs) / Service Level Agreements (SLAs) to strive for continuous improvement measures.
  • Demonstrates exceptional organizational skills, with the ability to efficiently multitask and manage one's own workload effectively, ensuring timely completion of tasks and adherence to deadlines in a dynamic environment.

About our future employee


You should speak English fluently and have experience in Validation Management, Quality Assurance or Quality Management.



Additionally, we are looking for:


  • Bachelor’s Degree; preferably in engineering, sciences, pharmaceuticals, or biotechnology or equivalent.
  • Good Knowledge of GxP (Good Practices) regulations.
  • Computer Systems Validation (CSV) knowledge would be a strong asset
  • Experience with Master Data or Reference Data would be an asset.
  • Experience in Test and Change Management would be an advantage.
  • Experience with Agile methods (e.g. SCRUM, Kanban) and tools (e.g. JIRA) would be an advantage.
  • Agile, accountable, and entrepreneurial mindset with a dedicated solution and result orientation.
  • Good analytical capabilities and problem-solving competence including a proper understanding of prioritization.
  • Dedicated team player with good communication skills, and a structured way of working.
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