Global Regulatory Affairs Senior Associate - Slough, United Kingdom - Reckitt

Reckitt
Reckitt
Verified Company
Slough, United Kingdom

4 weeks ago

Tom O´Connor

Posted by:

Tom O´Connor

beBee Recruiter
Description

Want to see your expertise recognised? As a
Global Regulatory Associate - NPD Durex you'll have the freedom to influence decisions that shape our next generation of leading brands.


Global Regulatory Associate - NPD Durex

Slough, Hybrid Working

Competitive Salary & excellent benefits package: 25 Days Annual Leave, Bonus, Private Health, 10% Pension Contribution
***You will enable delivery of NPDs to global markets by providing key skills and expertise in dossier creation, as an associate you'll work to support an integrated approach to regulatory planning across innovation and will provide SME knowledge and the latest information on dossier/technical file requirements. Development of the regulatory strategies for the assigned projects with a commercial mind set, working with the Regulatory Manager in driving regulatory expertise and understanding at feasibility and throughout the project. Collaborate with LRA to define development plans and timings of projects and critical regulatory parameters in data and timings.


You'll succeed because
you're degree qualified in a scientific discipline


Responsibilities include:

  • Work in partnership with the local regulatory teams to identify and be aware of key requirements and that they are taken into account to deliver a 'right first time' approach to new product development.
  • Responsible for delivery of dossier/technical file to agreed time frames and collaborate across partner functions to ensure timely deliver of all information required, to enable robust and consistent project updates.
  • Ensure high quality and accuracy of the dossiers vs the agreed requirements and highlighting of any potential issues, working with the authoring functions and LRA.
  • Supports work required to refine Regulatory processes and procedures to optimise accuracy and efficiency, thus enabling speed to market.
  • Provide through dynamic resourcing appropriate support (Subject Matter Experts) to the Innovation projects & team when assigned by manager.
  • Regulatory Experience and knowledge in NPD and dossier/technical file creation and global registrations / Medical Devices
  • Knowledge of the Regional and Global regulatory environment and how it impacts regulatory dossiers and registration
  • Experience in preparing and submitting dossiers, variations and renewals.
    You'll love it because
you'll have the freedom to make a difference. You'll put your own ideas into practice. The products you get out there will allow people to live healthier lives and have happier homes. And our dynamic, ownership-driven culture will bring the very best out of you, every day.


Equality:

At Reckitt, we recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience.

Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.

Come and join a team whose purpose is to protect, heal and nurture in the relentless pursuit of a cleaner and healthier world.

All qualified applicants to Reckitt will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

More jobs from Reckitt
See all jobs of Reckitt