Regulatory Manager (m/f/d)

☞ mamgo

Ver: 208

Dia de atualização: 25-04-2024

Localização: Aesch (BL) Basel-Landschaft BL

Categoria: Legal / Contratos

Indústria: Internet Publishing

Posição: Associate

Tipo de empregos: Full-time

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Conteúdo do emprego

My duties
  • Provide regulatory support to company submissions (Pharma and/or IVDR)
  • Effectively address regulatory issues that may surface during regulatory reviews and prepare and facilitate preparation of responses to Authorities in various Countries worldwide
  • Identify and prepare high-quality RA documentation and correspondence during registration and maintenance phase
  • Comply with applicable SOPs,

My Qualifications
  • BS or MS with requisite experience and demonstrated capability
  • Fluent English required (oral and written)
  • Relevant regulatory experience in Pharma and IVD
  • Strong ability to construct persuasive scientific/regulatory documents.
  • Strong ability to interpret scientific and commercial information
  • Strong interpersonal skills, team player

My Benefits
  • A very renowned company

About Hays

With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

My contact at Hays

My contact person

Marc Peter Linder

Contact

E-Mail: marc.linder@hays.ch

Reference number

598180/1
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Data limite: 09-06-2024

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