Regulatory Affairs Associate - Newry, United Kingdom - Norbrook Laboratories

Tom O´Connor

Posted by:

Tom O´Connor

beBee Recruiter


Description
In Norbrook we pride ourselves in being one of the top companies in Northern Ireland and

one of the top veterinary pharmaceutical companies globally. We develop & manufacture

veterinary medicines, supplying products to 120 countries globally. With a strong portfolio of

existing products and significant investment in R&D to launch new products annually, we

have opportunities for individuals to join us and develop their career in a global company.

Our business strategy is supported by our Values - Customer Value, One Team, Results

Driven, Excellence, Innovation, and Quality - and we support our employees to live the

behaviours that creates our culture. Our on-going success is based on the expertise,

knowledge and innovation of our employees. If you are interested in joining our team here at


Regulatory Affairs Associate

Job Overview
To assist in registration and maintenance of Veterinary Medicinal Products worldwide

**Main Activities/Tasks
Customers worldwide.

and approval processes.

  • Maintenance and updating of existing authorisations.
  • Responding to external queries from regulatory authorities and customers within strict
deadlines.

  • Working closely with all departments within Norbrook, providing regulatory support for
the operations and control of the facility.

  • Analysing scientific data and presenting the information in an organised format.
  • Work closely with Customers to ensure all issues are addressed in an efficient and
accurate manner.

  • Any other duties as deemed necessary by management.

Essential Criteria:


form in order to be considered:

  • Educated to a third level qualification or higher in Science, preferably a life science.
  • Excellent organisational skills along with a proven ability to meet deadlines.
  • Meticulous approach and attention to detail with a commercial insight and excellent
communication and negotiation skills.

  • Ability to work under his/her own initiative and as part of a dynamic regulatory affairs
team.

  • Ability to analyse scientific data and present this information in an organised format.
  • IT skills, particularly in relation to Powerpoint, Adobe and Excel.

Desirable Criteria:

Due to the nature of the role preference will be given to applicants demonstrating the


following desirable criteria:

  • At least 2 years' experience in the pharmaceutical industry or demonstrate relevant
experience.

  • Basic knowledge of local, European and Global pharmaceutical regulations of
medicinal products.

  • Technical file and documentation experience.
  • Project Management skills.

Duration:
Full Time, Permanent


Location:
Newry


Additional Information:


  • Applicants should be able to provide proof that they have a right to work in the UK at
be considered.

accepted


Benefits:


  • Free Life Assurance
  • Employee Assistance Programme


  • Company Pension Scheme

  • Onsite free parking


  • Healthcare cash plan

  • Canteen Facilities
  • 32 days annual leave Employee Perks scheme


  • Wedding Leave

  • Employee Recognition scheme


  • Company Sick Pay

  • Career development opportunities
  • Employee wellbeing initiatives

_Norbrook Laboratories Limited employs a workforce with members of all sections of _

_the community and is committed to appointing people purely on the basis of merit. In _

_accordance with our equal opportunities policy, we would particularly like to welcome _
**_applicants from the Protestant Community._

More jobs from Norbrook Laboratories