Regulatory Affairs Senior Associate - Cosmetics- 7 Month Fixed Term Contract

工作内容

Perrigo Company is dedicated to making lives better by bringing Quality, Affordable Self-care products that consumers trust everywhere they are sold. Help us do it.

Description Overview

7 Month Fixed Term Contract

This role can be based in any of the following locations: Ghent, London, Paris

In this role you will work on Regulatory Affairs projects as required to meet business needs

It will also be crucial to ensure compliance with Cosmetic Regulation 1223/2009/EC & other regulatory requirements and assist in any area of regulatory affairs at central level.

Hybrid Working Schedule, a mix of onsite and remote working.

Scope of the Role

• Work as part of a multi-functional team by providing regulatory input to new product development, including artwork approvals, label claims and associated supporting documentation
• As part of the team support the process of the notification/registration of Cosmetic products
• As part of the team ensure product notifications/registrations are correct and compliant with the relevant legislation.
• Participate to category and project meetings
• Establish, maintain, review, approve and update of Product Information Files in compliance with the Cosmetic Regulation 1223/2009/EC
• Approve Master Texts, LATs and promotional materials from a regulatory perspective
• Liaise with local affiliates, responding to regulatory queries and providing and review of registration documents as necessary for the European territory
• Communicate with local and international regulatory authorities regarding license applications and compliance issues and notice of change
• Interpret and implement (inter)national legislation, follow changes in (inter)national regulations and legislations and proactively manage and communicate impact of these changes
• Provide input for analysis of data and/or management review, if required
• Assist in the process of reporting and investigating critical non-conformities and opportunities for improvement
• Support on report and follow-up of change control / corrective / preventive actions if necessary
• Assist in performing internal audits, supplier audits and customer audits if necessary
• Carry out other related regulatory affairs duties as required
  
  

Experience Required

• Bachelor or Master’s degree in International Law, European Policies, Medical/Life Sciences or other relevant fields
• Postgraduate qualification desirable
• 2+ years of experience in a relevant regulatory environment
• Self-motivated, flexible and open to changing requirements
• Highly driven with enthusiasm to meet requirements and cope under demanding pressure
• The ability to work autonomously and in team
• The ability to lead and support several concurrent projects/products
• The ability to priorities decisions and activities to ensure efficient use of resources and address critical issues impacting the business
• Excellent project management and administrative skills
• Excellent communicator in English. Additional language skills are preferred.
• Excellent problem solving skills.
• Passion for products and regulatory compliance management
• Thorough and focused personality
• Have a strong entrepreneurial spirit
• Interested in innovation and creative thinking
  
  

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. Our full Equal Employment Opportunity and Affirmative Action Policy Statement is available on our main career site in English and Spanish and will be provided in other accessible forms for persons with disabilities. #DIV