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Regulatory Affairs Specialist

  • Job type: Permanent
  • Location: Kiel, Schleswig-Holstein
  • Salary: Negotiable
  • Job reference: 426983/001_1555070799
  • Sector: Medical Affairs, EPM Scientific
  • Date posted: 12/04/2019

Regulatory Affairs Specialist (Permanent position)

Job type: Permanent

Location: Schleswig - Holstein

Salary: Competitive

A leading reputable Medical Device company is currently seeking to hire a Senior Regulatory Affairs Specialist to join their growing team in Schleswig-Holstein. Employees will add value to the ever-growing Medical Device industry by contributing towards developing and improving regulatory affairs in the Medical Device industry.

Key responsibilities of the Regulatory Affairs Specialist include:

  • Ensure EU and international regulations by collaborating with other departments such as product development, quality management, marketing and customers.
  • Writing and improving technical documentation, which includes clinical evaluation.
  • Encourage and innovate the development of regulatory affairs.
  • Analyse documentation and providing feedback to other departments and regulatory staff.
  • Carry out risk assessment on the documentation.

Key requirements of the Regulatory Affairs Specialist include:

  • The ideal candidate should have an engineering or science background.
  • 4+ years of experience in Medical Devices.
  • A consolidated understanding and knowledge in regulatory affairs in the Medical Device industry e.g. MDD, MDR, Risk Management, Clinical Evaluation.
  • A bachelor's degree.

Benefits:

  • Great bonuses available depending on performance.
  • A great allowance on a company's car.
  • Health-care and pension schemes available.
  • Potential relocation package.

If you are interested in the manager position, apply online today or contact Melissa Wong at +44 203 6678383 for more information.

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