Are you ready to make a significant impact in the field of regulatory affairs? Join our team as a Regulatory Affairs Consultant with a focus on REACH dossiers. We are seeking a talented individual who can bring their expertise and enthusiasm to contribute to our dynamic and professional work environment.
Your Key Responsibilities
- Collaborating with internal teams regulatory authorities, and external partners to ensure a clear understanding of regulatory requirements and timelines.
- Overseeing and managing the preparation and submission of REACH dossiers ( Registrations and Notifications) for our products.
- Developing and implementing regulatory strategies to ensure the timely and successful registration of substances under REACH.
- Keeping abreast of updates and changes in REACH regulations and other relevant regulatory frameworks, and advising the organization on necessary actions.
- Maintaining accurate and comprehensive regulatory documentation and records.
Skills and required experience
- Previous experience in REACH regulation and guidance ( at least 3 years) , ideally in a consultancy role
- Experience in redaction of registration dossier, redaction of CSR (including use of risk assessment models for exposure scenarios) and identification of relevant studies needed for registration process.
- Excellent knowledge of relevant regulatory guidelines (EU Reg 1907/2006, EU Reg 1272/2008)
- Scientific background
- Flexibility, polyvalence, and pro-activity
- Solution minded
- Good knowledge of English, any other language is an asset.
How to Apply:
If you are a highly motivated and experienced Regulatory Affairs Specialist with a focus on REACH dossiers, we invite you to submit your resume and a cover letter detailing your relevant experience to [email protected]
Please include "Experienced Regulatory Affairs consultant- - REACH" in the subject line.
RRA is an equal opportunity employer. We encourage candidates from all backgrounds to apply.
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