Regulatory Affairs Specialist (m/w/d) Marketing Material

☞ Thermo Fisher Scientific

View: 183

Update day: 07-10-2024

Location: Hennigsdorf Brandenburg

Category: Other

Industry: Pharmaceuticals Biotechnology

Job type: Full-time

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Job content

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $30 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 80,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon.

As one of the largest biotechnology companies in Germany, we research, develop and produce innovative biomarker diagnostics and distribute our products in more than 65 countries. B
  • R
  • A
  • H
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  • S is based in Hennigsdorf near Berlin, which is home to about 285 of the company’s 550 employees worldwide.
As Regulatory Affairs Specialist (m/w/d) Marketing Material you are responsible for the regulatory review and approval of marketing, educational and commercial materials in the various life cycle phases of our products. Working remotely is possible.

What You Will Do
  • You are part of an international team and provide regulatory input on planned marketing, commercial and educational material covering digital and printed material such as online marketing, web page creation/update, social media, training presentations, brochures and review and approve that material.
  • You ensure consistency of claims according to registrations of IVDs internationally during the entire product life cycles.
  • You monitor international laws and regulations related to materials.
  • You support and develop review processes and procedures to meet both regulatory and business objectives.
What We Are Looking For
  • University degree in the field of life science, engineering or technical training (MTA, BTA, PTA) with appropriate further training or professional experience.
  • 3 to 5 years professional experience in the field of regulatory affairs.
  • Professional experience in the segment "In-vitro" diagnostics and marketing material desirable.
  • Solid knowledge of 21 CFR 820 and IVDR and technical product standards.
  • You have excellent organizational skills and are a strong communicator and enjoy working in a team with different cultures.
  • Hands-on, excellent command of written and spoken English.
What We Offer
  • Employment with an innovative, future-oriented organisation
  • Outstanding career and development prospects
  • Company pension scheme and other fringe benefits
  • Exciting company culture which stands for integrity, intensity, involvement and innovation
If you are interested please apply online with your CV and Motivation Letter including possible start date and salary expectations.

At Thermo Fisher Scientific, each one of our 80,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or any other legally protected status.
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Deadline: 21-11-2024

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