Average salary: €39,500 /yearly
More statsSearch Results: 35 vacancies
...the Executive Director of Global Patient Safety (GPS) within our Quality and Compliance Centers of Excellence (CoE). As the GPS Pharmacovigilance Intelligence Leader, you'll become a central figure in ensuring patient safety by navigating the evolving landscape of international...
...On behalf of my client, a global pharmaceutical company, we are working with them on a new role for a Pharmacovigilance and Clinical Quality Specialist.This is a full-time permanent role based in Dublin.
The Role & Responsibilities:
The main purpose of this cross functional...
Cpl Healthcare
Dublin
1 day ago
...in business discipline with associated experience in a regulated life sciences environment.
~ Proven experience working in a Pharmacovigilance Project Management environment.
~ Formal project management qualification or accreditation would be preferred.
~ Excellent communication...
Arriello Group
Ireland
4 days ago
...information, please visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter.
Brief Description:
~To lead Jazz’s Pharmacovigilance QA (GvP) function to assure regulatory compliance and data integrity in all Jazz activities related to Pharmacovigilance.
Essential...
...Deputy Qualified Person for Pharmacovigilance (Deputy QPPV)
Reporting to the Qualified Person for Pharmacovigilance (QPPV), the Deputy Qualified Person for Pharmacovigilance (Deputy QPPV) is responsible for assisting and providing back up to the QPPV in the day-to-day European...
Bimeda, Inc.
Ireland
1 day ago
£42.7k - £47k per annum
...landscape and review of medical device reports and product recalls.
* Collaborate with Device Development colleagues, Clinicians and Pharmacovigilance teams to analyse, evaluate, mitigate and control risks at the user interface in line with international standards and our...
Dublin
1 day ago
...cumulative and emerging data on the risks of medicinal products from various post marketing sources including clinical studies, pharmacovigilance databases and scientific literature to facilitate the timely detection and assessment of any safety concerns.
-Consideration...
...well as product information and artwork management. Furthermore, you will collaborate with various internal stakeholders such as Pharmacovigilance, Quality Assurance, and Supply Chain, while also beginning to develop external relationships and networks across other companies...
..., with alignment with areas of strategic research interest for relevant products/therapeutic areas.
Ensure that an effective Pharmacovigilance system operates within the affiliate, and that reporting requirements to competent authorities for adverse events and other safety...
...and the latest IPHA Code of Practice)
~Declares immediately any adverse event or quality complaint to the responsible person for pharmacovigilance or quality control in accordance with the applicable laws, rules and regulations
~Ensures budgets, timelines, compliance...
...and experienced Senior Principal Microbiologist for a permanent role. The successful candidate will play a crucial role in global pharmacovigilance activities related to our investigational products portfolio. This includes reviewing and analysing safety data from non-...
...complying with all applicable company policy and procedures.
Report all adverse events and product complaints promptly in line with Pharmacovigilance procedures and current legislation.
Able to educate and communicate clearly while building a good rapport with patients...
...Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.
Function as a subject matter expert internal and...
...governance for GPS Safety Sciences deliverables including, but not limited to, Risk Management Plans, Signal Management, and the Pharmacovigilance System Master File.
Establish and refine key performance indicators to ensure overall quality and compliance with associated...
...report immediately any untoward events on a patient visit. Report all adverse events and product complaints promptly in line with Pharmacovigilance procedures.
Application Criteria:
Must be registered with NMBI (Nursing Midwifery Board of Ireland)
Minimum of 3...
...or in a Clinical Development role. Strong Expertise with transferable skills related to Good Clinical Practice(GCP), and/or Good Pharmacovigilance Practice (GVP).
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an...
...Cork Validation Specialist - 50/50 remote
Carlow QA Compliance Specialist
Dublin Electronic Design Engineer
Galway Pharmacovigilance Manager (Remote)
Republic of Ireland Senior Regulatory Affairs Specialist
Dublin Recruitment Consultant
Wexford Senior...
Life Science Recruitment
Galway
5 days ago
...relationships in order to progress regulatory activities.
Liaise closely with Business Development (where required), Regulatory Science, Pharmacovigilance, Product Launch, Artwork, Supply Chain and Quality colleagues to ensure alignment in all initiatives.
Prepare regulatory...
Viatris
Dublin
2 days ago
...create reports when required.
Forward any incoming reports (whether it is through post, e-mail, fax or in Person) regarding Pharmacovigilance / Adverse Action Report to the relevant QPPV in a timely manner.
COMPETENCIES:
Organisational skills, personal efficiency,...
Chanelle Group
Galway
5 days ago
...jazzpharmaceuticals.com and follow @JazzPharma on Twitter.
Brief Description:
The Manager of Quality & Compliance (Q&C) for Pharmacovigilance (PV) is responsible for performing quality assurance activities to ensure that Jazz is adhering to Global applicable regulations...
