Job Description
Our client, a fast growing commercially driven multinational pharmaceutical company with a strong portfolio of marketed products including an exciting Oncology portfolio, now seeks a Regulatory Affairs Lead. This is a permanent role and will operate from their Dublin office.
Scope: This hire will manage and lead Regulatory function on site, including overall responsibility for all marketing authorizations, while also working as part of a wider European / Global team participating and leading relevant Regulatory projects. This role will operate within a matrix organization, leading local Regulatory Affairs and representation of such at HQ level.
Offering: This is an attractive opportunity for an ambitious experienced Regulatory Affairs professional looking to grow their career within a Global function. Due to the nature of projects involved, this role offers global visibility for the successful candidate.
Requirements for Regulatory Affairs Projects Manager:
Bachelor of Science Degree. Masters Degree in Pharmacy or other similar Life Science discipline preferred.
5+ years Regulatory Affairs experience within the pharmaceutical industry, including directly dealing with regulatory agencies.
Knowledge of Regulatory landscape and procedures within national and international level.
Good communication, influential, planning and problem-solving skills.
Ability to build and manage close relationships with all relevant stakeholders.
Experience of drug development and pharmaceutical marketing.
Excellent commercial acumen.
Please contact; Larry on 01-2302400 / larry@rftgroup.ie
The RFT Group, Biopharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors. www.rftgroup.ie
Key words; Regulatory Affairs, Regulatory Compliance, Marketing Authorisations, New Product Development, Pharmaceuticals, Dublin, Greater Dublin, Europe, Ireland.