Senior Chemical and Material Specialist

Rosówek

We are seeking a dedicated and experienced Senior Chemicals and Materials Specialist to join our Regulatory Compliance team, supporting the development and manufacturing of the future audiometric medical devices. You will play a key role in ensuring chemical and material compliance across all Demant Diagnostics brands.

Working from our Rosówek office, you will collaborate closely with colleagues in both Rosówek and Middelfart, Denmark, where your direct manager is based. The position offers flexibility in working hours and the option for hybrid working.

Working with us you will receive:

Full-time position (permanent contract) with a hybrid work model.
Scandinavian work culture. We are informal and care about equality, independence, an open dialog, work-life balance and teamwork.
Possibility for growth and opportunities to shape and define compliance strategies across the Demant Diagnostics brands.
Truly fantastic colleagues. We are an international team based in Poland and Denmark.
Benefits package (private medical health care, insurance, sport card, etc.).

What tasks are waiting for you?

Define and maintain the scope of chemicals and materials compliance across all Demant Diagnostics brands.
Establish, drive and ensure material compliance with applicable global regulations, including REACH and RoHS.
Ensure product biosafety through adherence to ISO 10993-1 standards.
Act as the primary contact with external laboratories for planning, coordinating, and following up on ISO 10993-1 testing.
Provide regulatory input on materials and chemicals during product development, change management, and supplier evaluation.
Collaborate across departments (e.g., R&D, Product Management, Procurement) to align compliance efforts.
Stay up to date on evolving global material and chemicals regulations within the medical device industry and assess impact on products and processes.

Apply today if you:

Have a degree in materials science, chemistry, chemical engineering or similar.
Have 3+ years of relevant experience in regulatory compliance or materials science, preferably within the medical device industry.
Posses strong knowledge of REACH, RoHS, and ISO 10993-1.
Are experienced in working with or managing external laboratories for biocompatibility testing.
Are able to work independently and across international teams.
Have strong organizational and communication skills in English (both written and verbal).

Ready to make an impact in medical device compliance?
Apply now and help ensure that our innovative products meet the highest global safety and regulatory standards.

For questions regarding the position, please contact Anders Damkjær Bæk, Regulatory Compliance Manager, Global Quality, Diagnostics – aekb@dgs-diagnostics.com

Furthermore we would like to inform you that the company has an internal reporting procedure, which is available at: demantcompliance - Make a report (codeofconduct.app)

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