Global Regulatory & Operations Lead
- Dublin
- Contract
- Drug Safety / Pharmacovigilance
Our client is a global supplier of sterile Injectable pharmaceutical products. They currently market and distribute a portfolio of sterile injectable drugs. Our state-of-the-art research and development organization has a robust pipeline of products in development that we will bring to regulated and semi-regulated markets around the world. These include dosage forms in multidose vials, multiple presentations within the blow-fill-seal offering, and small molecule cytotoxic products.
Responsibilities
- The need for an understanding of HPRA BoH requirements for hosting a market
- authorisation.
- Act as a Responsible Person for a Market Authorisation filing
- Manage & engage with Global Regulatory colleagues & stakeholders.
- Communicate & coordinate venders/ service providers - aligning activities & timelines.
- Build a quality system to manage the MA filing that meets HPRA requirements.
- Capable of supporting a WDA for release of product into Europe.
- Regulatory Affairs experience in dossier creation and submission in Europe.
- Represent the company as the lead person with all the relevant local authorities.
- Manage Regulatory Affairs activities associated with changes to MAs for all products
- registered in the territories under his/her responsibility
- For MAs, directly manage:
- Creation, maintenance and management of MAs
- current registered details
- Build relationships & coordinate with product CMO's & wholesale distributor.
- Pharma – 380 staff located in Perth.
Your Experience
- 8-10 year years of professional Regulatory Affairs experience in the Pharmaceutical
- industry
- Experience working with the HPRA
- Experience reviewing regulatory dossiers
- Excellent communication and stakeholder management skills
- Experience working with global teams & Regulatory Authorities
If this role is of interest to you, please apply now!
#LI-KT1
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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