Regulatory Affairs Manager - CMC

Location: Dublin, Republic of Ireland
Salary: Negotiable
Posted: 3 months ago
Role type: Permanent
Industry: Science, Technology and Operations Practice (STO), Science Leaders & Specialists
Contact name: Gillian McMurrough
Contact email: gillian.mcmurrough@hrmrecruit.com

Job description

Our client is one of the world's leading biopharmaceutical companies. Due to continued growth and success, they seek to hire an experienced RA - CMC professional to join their Regulatory Affairs department based at their state of the art manufacturing facility in Dublin. My client pride themselves on promoting a culture of innovation and putting the need of the patient first.

The Role:

The RA Manager will report into the Senior Manager within the group. Main activities will include:

  • To develop and implement CMC regulatory strategies and support CMC RA activities for products manufactured at the site.
  • To contribute to and offer RA expertise for products manufactured at external sites globally.
  • To contribute to product development and NPI projects across the business.

The Person:

In order to be considered you must have the following:

  • A third level degree in Science, Engineering or related.
  • 3+ years RA industry experience - within the Biotechnology or Pharmaceutical space.
  • CMC experience and expertise - essential.
  • Strong communication skills and an ability to work effectively in a team and cross functionally.
  • Excellent project management skills.
  • Eligibility to live and work in the EU.

To discover more about this opportunity, apply now or contact Gillian McMurrough at HRM on +353 87 1213548 for a confidential discussion.


Gillian Mc Murrough

Associate Director - Science

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