Regulatory Affairs Specialist in Part-time

Vor 3 Tagen

Bayreuth, Bayern, Deutschland medi GmbH & Co. KG Vollzeit

Job Summary:

We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at medi GmbH & Co. KG in Bayreuth. As a Regulatory Affairs Specialist, you will play a key role in ensuring the compliance of our medical products with regulatory requirements.

Key Responsibilities:

  • Support the Regulatory Affairs team in all aspects of regulatory affairs, including regulatory submissions, compliance, and quality management.
  • Identify and monitor national and international regulations, laws, and guidelines.
  • Develop and implement regulatory strategies to ensure compliance with regulatory requirements.
  • Collaborate with cross-functional teams to ensure regulatory requirements are met.
  • Prepare and submit regulatory documents, including quality management system documentation.

Requirements:

  • Bachelor's degree in a relevant field, such as law, business, or medicine.
  • Proven experience in regulatory affairs, quality management, or a related field.
  • Excellent knowledge of medical device regulations and quality management systems.
  • Strong analytical and problem-solving skills.
  • Excellent communication and teamwork skills.

What We Offer:

  • A dynamic and supportive work environment.
  • Opportunities for professional growth and development.
  • A competitive salary and benefits package.
  • The chance to work with a leading medical device company.

About Us:

medi GmbH & Co. KG is a leading manufacturer of medical devices and solutions. We are committed to delivering high-quality products and services that improve the lives of our customers. Our team is passionate about innovation, quality, and customer satisfaction.

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