Senior Regulatory Affairs Officer | Collins McNicholas

Senior Regulatory Affairs Officer

  • Reference: 44736
  • Job Type: Permanent
  • Location: Dublin South, Dublin West, Kildare
  • Category: Science, Pharmaceutical & Food

New position – seeking a Senior Regulatory Affairs Officer – DUBLIN – City West – Permanent

Key Deliverables.

  • Obtain and maintain all necessary licences (Marketing Authorisations (MA’s), Clinical Trial Authorisations (CTA’s) Etc.) for a designated list of products.
  • Maintain an awareness of current Irish & EU regulatory requirements.
  • Deputise in the absence of the Head of Regulatory Affairs.Submit applications (new MA’s/Clinical Trials/Variations/Renewals etc.) for National/EU MA ‘sand negotiates with the Health Products Regulatory Authority (HPRA) to resolve any issues to minimise the delay in approval.
  • Ensure prompt resolution of regulatory issues affecting the Irish business.
  • Communicate significant regulator issues/developments to commercial and the potential impact on the Ireland business.
  • Liaise with other sites UK, European and Global groups on regulatory issues as relevant.
  • Liaise and attend meetings with other company functions to provide regulatory advice for new products, indications, promotional campaigns etc.
  • Review of product information and promotional material prior to re lease.
  • Cover all Regulatory aspects of pharmacovigilance.
  • Maintain compliance of regulatory based labelling (Summary of Product Characteristics (SPC), Package Leaflet (PL) and Prescribing Information (PI)).
  • Maintenance and update of all internal required reporting activities and databases 
  • Maintain awareness of current and new legislation/ guidance and ensure that work is in compliance with the requirements.
  • Develop and maintain regulatory Standard Operating Procedures (SOP’s) as required and provision of regulatory support during inspections and audits.Strategic Input & Regulatory Intelligence:
  • Provide strategic regulatory input and support to the Ireland business.
  • Build relationships with the HPRA, Irish Pharmaceutical Healthcare Association (IPHA) and other relevant organisations and personnel both internally and externally.
  • Gain regulatory approvals by appropriate negotiation with the HPRA and/or EU and Global groups.
  • Anticipate and monitor changes in National and EU regulatory requirements in order to contribute effectively to product development and regulatory strategies.
  • Monitor the regulatory landscape for generic, parallel import and competitor activity as relevant.

 

For this role, you should have:

  • A Third level degree qualification in Life Science or similiar
  • 4 years’s plus experience of working in a regulatory position is ideal
  • Knowledge and experience of GDP and GCP regulatory environments would be beneficial
  • Excellent team working and communication skills
  • Strong negotiation, influencing, presentation skills
  • Strong visionary, strategic, tactical and motivational skills
  • Avialable to travel – circa 5% of the time.

 

For a confidential discussion and or more information on the role, please contact Mary Mullin  on 09064 78104  / 085 871 8281 or email mary.mullin@collinsmcnicholas.ie

For more information on our Recruitment and HR Services and to see a full list of our available jobs across Ireland, please visit our website www.collinsmcnicholas.ie

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Contact Consultant

  • Mary Mullin
  • Regional Manager
  • 09064 50661
  • Connect with Mary

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