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Pharmaceutical Operations Lead

1 week ago

Portlaoise, Laois, Ireland Quanta Consultancy Services Ltd Full time

**Key Responsibilities**

  • Act as a Responsible Person for a Market Authorization filing
  • Manage & engage with Global Regulatory colleagues & stakeholders
  • Communicate & coordinate vendors/service providers - aligning activities & timelines
  • Build a quality system to manage the MA filing that meets HPRA requirements

The ideal candidate will have 8-10 years of professional Regulatory Affairs experience in the Pharmaceutical industry, excellent communication and stakeholder management skills, and experience working with global teams and regulatory authorities.