Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Regulatory Affairs Copy Review Specialist

Posted Feb 11, 2021
Job ID: JJJP00005756
6 months
(Feb 25, 2021 - Aug 24, 2021)
40 hrs/week
Payrate range
18 - 20 £/hr

Regulatory Affairs Copy Review Specialist

6 month contract


Drawing on relevant expertise and information from both internal and external sources, responsible for the review and approval of promotional and advertising assets and professional education resources for hospital Medical Devices.  

Key Responsibilities:


  • Supporting all business across the HMD group of companies in reviewing and approving copy review of assets 
  • Setting and communicating timelines for approvals with commercial partners. 
  • Working to strict deadlines provided by the commercial partners. 
  • To work with other members of the team to increase knowledge on products. 
  • Reviewing company practices and providing advice on changes to systems.   


Experience required:


  • Successful graduation in a Life Science degree or equivalent 
  • Proven copy review experience in medical devices 
  • Proven knowledge of the ABHI Code of Conduct 
  • Strong Attention to detail
  • High degree of initiative 
  • Team player, fosters the strength of a network 
  • Well organised
  • Experience in Copy Review 
  • Able to cope with fluctuating and high work-load demands 

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