Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
Job Function:
Product SafetyJob Sub Function:
PharmacovigilanceJob Category:
Scientific/TechnologyAll Job Posting Locations:
Bratislava, Bratislava, SlovakiaJob Description:
- Act as LSO for Johnson&Johnson Innovative Medicine medicinal products in Slovak Republic.
- Act as LSO back-up for Johnson&Johnson Innovative Medicine medicinal products in Czech Republic.
- Act as Nominated Person Responsible for Pharmacovigilance /local contact person for Slovak Republic.
- Act as Nominated Back-up of Responsible Person for Pharmacovigilance/local contact person for Czech Republic.
- Ensures that all corporate requirements as well as local legislation on adverse reporting are followed.
- Provides regular training on pharmacovigilance to all relevant J&J employees.
- Ensuring that the LOC PV activities are managed in compliance with local regulations and company policies/procedures at a local, regional and global level and in accordance with any PV agreements with third party business partners.
- Have an appropriate system of PV and Risk Management in place to assure appropriate oversight for products within their responsibility
We would love to hear from YOU, if you have:
- Medical or pharmaceutical sciences with proven expertise and experience in pharmaceutical regulations and R&D processes is preferred.
- By preference a minimum of 2 + years pharmaceutical industry experience with at least 1 year in a PV responsibility role.
- Sound knowledge of general medicine or pharmacy and clinical practice, or relevant scientific/medical field.
- Proven ability to organize workflow activities and manage multiple critical issues.
- Awareness of and familiarity with industry principles of PV, drug development and pharmacology.
- Expert knowledge of Global, Regional and Local PV Procedural Documents as applicable.
- Computer literate with knowledge of relevant IT safety systems.
- Excellent verbal and written communication skills with proven ability to negotiate and communicate with internal and external customers.
- Ability to establish and maintain open relationships within the organization and with authorities.
- Demonstrable knowledge of all local PV requirements and of global aspects of drug safety.
- Fluency in the national language(s) and the English language is required
This is what awaits YOU at J&J:
- An opportunity to be part of a global market leader.
- A dynamic and inspiring working environment.
- Many opportunities to work on challenging projects and assignments.
- Possibilities for further personal as well as professional development.
Employee benefits are regulated by an internal policy that contains full details regarding the entitlement and conditions for the benefits.
We offer attractive conditions of employment and possibilities for further career growth within our company.