Senior Manager, Regulatory Affairs

Highly Competitive
  1. Permanent
  2. Project Manager
  3. Germany
Munich, Germany
Posting date: 03 Sep 2020
31570

At ProClinical we are looking to hire a Senior Manager of Regulatory Affairs to be based in Munich. This is a global pharmaceutical company and the role involves seeing projects through their late stage development to gaining marketing approvals and post-approval.

Job Responsibilities

  • Manage activities such as audits, regulatory agency inspections, or product recalls
  • Participate in the development or implementation of clinical trial protocols
  • Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced
  • Communicate regulatory information to multiple departments
  • Investigate product complaints and prepare documentation and submissions to appropriate regulatory agencies as necessary
  • Monitor emerging trends regarding industry regulations to determine potential impacts on organizational processes
  • Oversee documentation efforts to ensure compliance with domestic and international regulations and standards
  • Monitor regulatory affairs activities to ensure that they are aligned with corporate sustainability or green initiatives

Skills and Requirements

  • Degree in life science, medicine or pharmacy
  • Min. 2 years of experience in pharmaceutical environment
  • Very good command of English (both oral and written), as well as German
  • Thorough knowledge of guidelines
  • Problem-solving skills

To Apply

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Nico Kohlwes on +49 69 94189257 or upload your CV on our website - www.proclinical.com/send-cv

A full job description is available on request.

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