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Change Expert Regulatory Compliance (m/f/d) - Sterile Fluids - Bad Homburg, Germany

12 days ago


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Job Opportunity Details

Type

Full Time

Salary

Not Telling

Work from home

No

Weekly Working Hours

Not Telling

Positions

Not Telling

Working Location

DEU Bad Homburg - Global Headquarters, Bad Homburg, Germany, Germany   [ View map ]
  • Support of Product Center Sterile Fluids in cross-location activities to monitor product quality
  • Participation in new component / product development activities as part of Cross Functional Team, related to risk analysis activities and for providing regulatory expertise
  • Participation in risk management activities as team member for product risk analysis if applicable (participation for products, components, process in case of a design change)
  • Support creation/maintenance of risk evaluation documents for medicinal products or medical devices
  • Participation in regular quality meetings and preparation of relevant documentation
  • Support harmonization activities of Product Center Sterile Fluids

Main Responsibilities:

  • Leading regulatory or compliance changes change projects as project manager or supporting as team member for design change and compliance projects
  • Project management for the implementation of change projects to comply with regulatory requirements
  • Management of global teams within change projects
  • Expert and interface function to the development department, marketing, production, quality department, as well as to the regional/local approval unit
  • International coordination and communication in a global organization
  • Supporting the department in cross-site activities to monitor product quality and regulatory compliance

What we expect?

  • Successfully completed technical or scientific studies
  • Experience in project management respectively change control process
  • Experience in regulatory affairs or in a quality environment, ideally in a pharmaceutical/medical environment of advantage
  • Knowledgeable in relevant regulations (such as registration of medicinal products, change control, GxP, EU requirements, NMPA regulation, US FDA requirements, ASEAN, etc.)
  • Language requirements: Fluent in English, advanced in GermanStructured and independent way of workingStrong communication skillsAbility to work in and with a team
  • Assertiveness

Our offer to you:

There is a lot for you to discover at Fresenius, because we have a lot to offer. No matter in which field you are an expert (m/f/d) and how much experience you bring with you - for your professional future with meaning:

  • The opportunity to work on a mobile basis
  • Whether in front of or behind the scenes - you will help to make better and better medicine available to more and more people around the world
  • Individual opportunities for self-determined career planning and professional development
  • A corporate culture in which there is enough room for innovative thinking - to find the best, not the fastest, solution together
  • A large number of committed people with a wide range of skills, talents and experience
  • The benefits of a successful global corporation with the collegial culture of a medium-sized company

Please note that the offered role is currently limited to approx. 18 months.


More Information

Application Details

  • Organization Details
    DE01 DEU Fresenius Medical Care D. GmbH
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