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UK & IE Regulatory Affairs Officer

Date: Jan 8, 2021

Location: Harlow, GB, CM20 2FB

Company: Teva Pharmaceuticals

Who Are We?

We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point. Yet until today, you may not have heard of us.

We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.

We are looking for Regulatory Affairs Officer to join our UK & Ireland team to help obtain new marketing authorisations and maintain the existing licence portfolio. This role will allow the successful candidate to work with new submissions across generic, OTC and speciality sectors covering the full life cycle from initial submission.

A Day in the Life of….

  • You will prepare, compile, review and submit high quality regulatory dossiers, post-approval changes (variations, renewals, PIQU submissions) and respond to Health Authority questions in accordance with in-house standards and current legislation.
  • You will ensure approvals are secured within the stipulated timelines for designated projects.
  • You will maintain registration documentation and associated electronic databases, in line with in-house procedures.
  • You will provide regulatory support and product information for all internal and external customers, stakeholders and TEVA project teams.
  • You will prioritise, plan and monitor allocated projects against defined timelines.
  • You will maintain and develop awareness of current/pending regulatory legislation and guidelines
  • You will identify and initiate areas for process improvement, and manage changes as required.

Who we are looking for

Are you….

  • Able to work under pressure and to tight deadlines?
  • Able to manage your time effectively with strong prioritising and organisation skills?
  • Able to communicate clearly in both oral and written formats?

 

Do you have….

  • A Degree in either a Life Sciences or Pharmaceutical subject or equivalent experience within the Pharmaceutical industry?
  • Experience within Regulatory Affairs, Quality, R&D or Operations?
  • Knowledge of regulatory procedures within the UK, Ireland or other EU countries?
  • Experience using Trackwise or other document management systems?

What do we offer you?

  • 25 days annual leave plus Bank Holidays
  • Company bonus scheme
  • Flexible benefits including health insurance, gymflex and cycle to work scheme
  • Programme of Wellbeing initiatives including on-site Creative Rooms, Employee Assistance Programme, Wellbeing Champions

 

We are happy to talk about flexible working!

Function

Regulatory Affairs

Sub Function

Medical Regulatory Affairs

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.

Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients. That’s why we’re constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice.