Senior Expert Regulatory Affairs

Envalior

Not Interested
Bookmark
Report This Job

profile Job Location:

Dormagen - Germany

profile Monthly Salary: Not Disclosed
Posted on: 11 hours ago
Vacancies: 1 Vacancy

Job Summary

Description

Join Envalior Imagine The Future!

Are you passionate about driving regulatory excellence in a constantly evolving environment At Envalior we are seeking a talented Senior Expert Regulatory Affairs to join our dynamic team and help ensure our products meet the highest standards of compliance and safety across global markets.

At Envalior the future of high-performance materials isnt just being shaped; its being pioneered. A belief in fostering an environment where every voice is heard and ideas are valued is integral to our culture. Empowerment is the driving force behind our pioneering spirit allowing our teams to take initiative explore new solutions and revel in the thrill of constant innovation.

Join us and be a part of a team committed to making a positive impactwhere safety sustainability collaboration and empowerment intersect to drive innovation.

IMAGINE THE FUTURE WITH ENVALIOR

As a Senior Expert Regulatory Affairs at Envalior you will create and maintain regulatory information statements and documentation in compliance with international and country-specific legislation ensuring our products meet all relevant standards. You will actively support and maintain internal systems and databases to ensure regulatory and product safety compliance for raw materials and finished goods. Additionally youll embrace a pioneering spirit exploring new regulatory frameworks and data management approaches to contribute to our values and mission.

You will make key contributions to Envalior by:

  • Creating and maintaining Regulatory Data Sheets product regulatory quality declarations and other compliance documentation.
  • Supporting internal systems and databases to ensure product and raw material compliance.
  • Reviewing and interpreting regulatory legislation and advising on implementation.
  • Monitoring regulatory developments and providing guidance to internal stakeholders such as R&D Marketing & Sales Manufacturing SHE Logistics and Purchasing.
  • Identifying and addressing non-compliance issues within Envaliors product portfolio or raw materials.
  • Managing and maintaining global product data through up-to-date systems and defined workflows.
  • Releasing data and documents in global recipe systems


Requirements

THE IDEAL CANDIDATE

  • Holds a degree in Chemistry or a related scientific discipline.
  • Has 510 years of experience in Regulatory Affairs or a relevant field.
  • Demonstrates strong attention to detail a structured and pragmatic approach and is highly self-motivated.
  • Possesses excellent English communication skills.
  • Proficiency in tools such as Power BI and Excel are a plus
  • Brings a customer-oriented mindset and the ability to see the bigger picture.
  • Is curious proactive and eager to grow into a broad regulatory expert role.


Benefits

WHY ENVALIOR

Competitive Compensation:

Join us at Envalior and enjoy competitive compensation packages inclusive of a global bonus program and performance bonuses ensuring your hard work is recognized and rewarded.

Comprehensive Benefits:

Your well-being matters to us. At Envalior we provide an array of benefits supporting your financial security health and overall well-being. This includes retirement plans health programs life insurance and comprehensive medical care.

Work-Life Balance & Flexibility:

Maintain a healthy balance between work and personal life with Envaliors commitment to supporting your schedule.

Training & Development Opportunities:

At Envalior your growth matters. We encourage and invest in your professional and personal development. We support our employees in their growth and personal development through ongoing investment in their knowledge and skills via training coaching and mentoring.

Diversity & Inclusion:

At Envalior our people drive our success so its only right that we provide a diverse and inclusive working environment and foster a culture of belonging openness and respect. We value diversity as a cornerstone of our success. We are committed to nurturing and empowering every individual to reach their full potential.

APPLY NOW!

Ready to pioneer change with Envalior Join us in our mission to drive innovation sustainability and excellence. Apply today and become a part of our transformative journey towards a more sustainable future.

Envalior is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race religion color national origin gender (including pregnancy childbirth or related medical conditions) sexual orientation gender identity gender expression age status as a protected veteran status as an individual with a disability or other applicable legally protected characteristics.

If you need assistance or an accommodation due to a disability you may contact us at

OUR HERITAGE

With a combined heritage of over 100 years Envalior brings together two established global materials players: DSM Engineering Materials and LANXESS High Performance Materials. Our unique combined portfolio of longstanding material- application- and design expertise enables our customers to develop and launch sustainable future-proof designs. Envalior is the brand new materials powerhouse that was Launched in early 2023.

We aim to be a global leader in sustainable and high-performance engineering materials. We imagine the future by shaping the world of today and tomorrow. Were conscious that this is both a privilege and a responsibility so when we imagine the future were guided by our key values to help us create a better world.


Required Experience:

Senior IC

DescriptionJoin Envalior Imagine The Future!Are you passionate about driving regulatory excellence in a constantly evolving environment At Envalior we are seeking a talented Senior Expert Regulatory Affairs to join our dynamic team and help ensure our products meet the highest standards of complian...
View more view more

Key Skills

  • Proofreading
  • Adobe Acrobat
  • FDA Regulations
  • Manufacturing & Controls
  • Biotechnology
  • Clinical Trials
  • Research & Development
  • GLP
  • cGMP
  • Product Development
  • Chemistry
  • Writing Skills

About Company

Company Logo

We offer a uniquely positioned portfolio of longstanding material, application, and design expertise, creating real and meaningful value for our customers and the greater society

View Profile View Profile