ABOUT ABBOTT

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
In Germany, Abbott has more than 4,000 employees working in manufacturing, research and development, logistics, manufacturing, sales and marketing. They are located at Abbott`s German headquarters in Wiesbaden and its sites in Hanover, Neustadt am Rübenberge, Wetzlar, Eschborn, Cologne, Jena and Hamburg.

QUALIFICATIONS

• Student of medical science or technology, bioscience or related.
• Basic knowledge of quality management systems and regulatory principles are desirable.
  Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
  

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We ask for your understanding that we only consider online applications via our online application portal. Applications by email or post cannot be processed. Original documents will not be returned.
Connect with us at www.abbott.com, on LinkedIn at https://www.linkedin.com/company/abbott-/, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal

MAIN PURPOSE OF ROLE

• Assists in developing an instruction or procedure to aid with the training on International registration requirements.
• Performs entry-level professional business support/administrative work, gradually increasing
• in level of difficulty and responsibility as on-the-job/formal training is received.

MAIN RESPONSIBILITIES

• Performs a variety of entry-level duties and assists higher-level personnel in regulatory related activities for the International Regulatory and Site Regulatory functions at the Wiesbaden site.
• Supports administrative work on department specific processes and procedures.
• Works independently on International regulations and QMS requirements and conducts interviews with International affiliates.
• Summarizes findings into an overview which can serve as a training document for site regulatory and quality personnel long-term.
• Prepares respective overviews and presentations to report the continued progress of the assigned activities.