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 Specialist - North West England - Remote

Posted May 7, 2021
Job ID: JJJP00006518
Location
Blackpool
Duration
11 months, 4 weeks
(May 24, 2021 - May 24, 2022)
Hours/week
37 hrs/week
Payrate range
15 - 25 £/hr

Regulatory Affairs Specialist - North West England - Remote


Please note: We are only considering candidates in the North West of England for this role. You may need to visit site occasionally!


The Company:

Johnson & Johnson is the world's most comprehensive and broadly-based healthcare Company, touching the lives of nearly a billion people every day. Our Family of Companies throughout the world compete in consumer, pharmaceutical and medical devices & diagnostics markets and have the skills and resources to tackle the world's most pressing health issues.


This role is working for DePuy Synthes. Working within the Regulatory Affairs, Global Strategy & Implementation department. Reporting to the Regulatory Affairs Manager, Strategic Markets


The Project:

Responsible for supporting regulatory activities and projects within Global Strategic Implementation across DePuy Synthes platforms in a timely manner in accordance with regulatory and company requirements.


Duties and Responsibilities:

  • Liaise with internal departments and worldwide regulatory colleagues to support registration activities for strategic markets.
  • Maintain regulatory and registration databases, including archiving, and analyze data to provide reports to immediate managers as required.
  • Support projects with Global Strategic Implementation such as UDI, Product Portfolio Management.
  • Creation of MDRIM regulatory strategies as required.
  • Responsible for ensuring compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance to enable the site to achieve and maintain excellent results.
  • Managing a significant amount of proprietary information in a confidential manner to prevent loss of intellectual property.
  • Provides solutions to a variety of problems of moderate scope of complexity.


Professional Experience Required:

  • Have worked in a Regulatory Affairs role before
  • Minimum of 2 years of related experience preferably Medical Devices or Pharmaceuticals


Education Requirements: 

  • Minimum of a B.A. /B.Sc. within a technical related discipline is prefered.  



Other Requirements:

  • Excellent planning and organizational skills.
  • Ability to pick up and work with new IT  systems quickly.
  • Ability to work both independently and in a team environment. 
  • Ability to problem solve, recognize and find solutions for gaps in processes
  • Communication – listener, learner and thinker.
  • Thorough and flexible.
  • Cross-culturally aware.
  • Team player.
  • Enthusiastic and committed.
  • Excellent knowledge of Microsoft office PC packages.
  • Excellent written and verbal reasoning skills.


In Return:

In return for this role you will receive a very competitive hourly rate. A minimum 12 month contract & an opportunity to work with a Global Leader within the Pharmaceutical sector, Johnson & Johnson. 


This role is remote however we are looking for candidates that are within a commutable distance to either Leeds or Blackpool as you may be required to visit the site periodically. 


Please Note: This role is INSIDE IR35. Pay rate for this role will depend on how you are paid (PAYE or Umbrella options) 


If you are interested in this role please apply now, or for more information contact Tabitha.Crabtree@randstadsourceright.co.uk


Please Note: Applications for this role will close Tuesday so be quick!

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