Regulatory Affairs Advisor
Initial 6 month contract
Offering up to 390 Per Day via PAYE
CPL Life Sciences is collaborating with a Top 10 Pharmaceutical firm who are looking for an experienced Regulatory Affair Advisor to support the submission of national dossiers and licence maintenance applications for local health authorities including the UK and Ireland. Within this role you will be responsible for regulatory activities relating to product launches and maintaining existing assigned product licenses.
Job Responsibilities include;
Preparation, QC and submission of national dossiers and licence maintenance applications to the local Health Authority (HPRA)
Facilitate approval of new product licences, indications and dosage strengths for the Irish market.
Support the regulatory activities relating to product launches.
Maintain local RA databases and Global compliance tracking systems to record local licence information (new indications, changes in indications, changes in product specifications, changes in licensing, new products and progress with development of new products).
Review and update all product labels and leaflets (artwork) for consistency with the licence for implementation according to required timelines
Candidate requirements include;
Eligibility to live and work in the United Kingdom
Life Sciences degree or equivalent
Prior Regulatory experience ideally 3-4 years regulatory experience in pharmaceuticals
Effective communication and negotiation experience
If this opportunity is of interest to yourself please forward your up to date CV to Sophie.Malyon@cpl.com.
- Agency: Cpl Life Sciences
- Reference: JO-2209-500213
Website: Cpl Life Sciences
- Posted: 2nd September 2022
- Expires: 30th September 2022