Our client, a US based health care company that develops innovative personal care products, is looking for an EMEA Regulatory Affairs Manager with hands-on RA experience for their EMEA Headquarters located in Brussels. You are offered a full time permanent contract in direct.
As an EMEA Regulatory Affairs Manager for 26 markets across the EMEA region, you will take on senior responsibilities in the team and you will have 3 direct reports.
Your main focus is to implement and lead regulatory projects to ensure compliance with the various regulations related to food supplements, electronic devices, REACH and sustainability.
You will lead, coach & develop 3 regulatory specialists and you provide guidance and training to all key stakeholders on relevant regulatory matters. It’s your goal to create an environment for talent development.
In addition, you are driven by obtaining the EMEA and global regulatory goals and objectives. It’s your responsibility to set up, implement and maintain efficient regulatory projects, processes and systems for all aspects in the regulatory product life-cycle.
Internal and external collaboration with the global and local stakeholders is daily business. You foster active communication and awareness of emerging issues and opportunities with internal key stakeholders (Marketing, Sales, Legal, Quality, Supply Chain).
In conjunction with global and local R&D and Marketing, you ensure that products are developed and validated to comply with the applicable EMEA legislative framework.
You understand the principles of Risk Management and you resolve post-market product related issues effectively.
Finally, you monitor the regulatory environment and anticipate changes.
You have a scientific bachelor or master degree and extensive knowledge of and previous hands-on experience in Regulatory Affairs related to food supplements, electronic devices, REACH, packaging and sustainability.
English holds no secrets from you and you can effectively and fluently communicate. Every other European language is considered a plus.
You are familiar with independently interpreting and evaluating the details in technical material and government regulations/policies and to turn technical jargon into easily understood information.
It’s a must that you have a proven track record in managing projects. And that you demonstrate genuine interest and enthusiasm for compliance and how it impacts the business.
Finally, if the words: ownership, team-player, planner and self-motivated; cover your personality, you are the person for this job!
You are offered a full time contract (CDI) on the client’s payroll and a challenging opportunity in a dynamic and open company where you will work close to the business and have international contacts.
The company offers you the opportunity to evolve and you contribute to the development of a successful, stable and growing team.
Not ready to apply or do you have questions first?
Please give me a call on +32 10 80 71 04, I’ll be happy to give you more information!
Clinical Recruitment eXPErt