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Interacoustics A/S

Regulatory Affairs Specialist

Middelfart

We are on an exciting path of growth and are currently seeking a new specialist to join our team and play a crucial role in ensuring that our operations adhere to relevant regulations and industry standards.

A significant part of your role will be to take regulatory ownership of selected product areas, and ensure the required activities take place, to ensure we are following current regulatory standards for medical device development.

Interacoustics A/S
Gem
Interacoustics A/S

Regulatory Compliance Specialist

Middelfart

Do you want to influence regulatory compliance and future medical product development in a global company that provides an attractive workplace for the industry’s best and brightest?

You will play an important role in ensuring that our products meet all regulatory requirements while upholding our commitment to quality and innovation.

A significant part of your role will be to take part in planning and implementing the required documentation, including usability engineering and risk management, in compliance with current regulatory standards for medical device development.

Interacoustics A/S

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