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(Senior) Regulatory Affairs Manager (m/w/d)

  • Salary: €75000 - €90000 per annum per year
  • Job Type:Permanent

Posted 12 days ago

  • Sector: Medical Technology
  • Contact: Daniel Perkins
  • Contact Email: d.perkins@sciproglobal.de
  • Start Date: ASAP
  • Expiry Date: 18 August 2021
  • Job Ref: DP 240660_1626704871

(Senior) Regulatory Affairs Manager - Substance Based Medical Devices (m/w/d)

Are you interested in working in an owner-managed, family-orientated, medium-sized organization? Do you enjoy short decision-making paths and the freedom to implement your own ideas? Is a hands-on approach to leadership appealing to you? If your answer to these questions is yes, then look no further!

Your responsibilities as the new (Senior) Regulatory Affairs Manager:

  • The preparation of international approval documents for substance-based medical devices (OTC class I - II), and the corresponding European and International registration processes.

  • The review and approval of approval documentation.

  • The maintenance of the company's regulatory compliance.

  • Relevant contact person for notified bodies/authorities, and internal/external customers regarding regulatory-related topics.

  • Responsibility for acting as the company's PRRC (§15 MDR) for regulatory aspects (technical documentation, post-market surveillance, reporting obligations).

  • Entrusted with leading responsibilities in interdisciplinary projects, as well as the technical guidance of more junior colleagues.

What awaits you as the new (Senior) Regulatory Affairs Manager?

  • Flexible working arrangements.

  • The possibility to work remotely (up to 90%).

  • A strong sense of creative freedom, allowing you to use your strengths optimally.

  • The possibility to work with global leading, cutting-edge pharmaceutical and medical device organizations.

  • Extremely flat hierarchies, with short decision-making paths.

  • Working in a family-orientated, friendly environment.

  • International customers and varied tasks

  • Company pension scheme

  • Subsidized canteen, with access to free fruit and drinks.

  • In-house fitness programs.

The ideal Director (Senior) Regulatory Affairs Manager would have the following qualifications:

  • Successfully completed a university degree in a scientific or technical field (or compatible qualifications).

  • Several years of working experience within the field of regulatory affairs for medical devices at national and international levels.

  • An in-depth understanding of all relevant standards, regulations, and requirements (MDD/MDR, ISO 13485, etc.).

  • A flexible, entrepreneurial work style paired with a structured and analytical way of thinking.

  • Ability to assess regulatory risks/benefits and applicable guidance.

  • Excellent command of both the English and German languages.

  • Willingness to travel up to 10%

I am looking forward to receiving your application and learning more about your profile!