Job Information
Bausch Health Director, Pharmacovigilance in Laval, Quebec
Bausch Health Canada is the international head office of Bausch Health Companies, one of the fastest growing international pharmaceutical companies dedicated to bringing quality health and wellness products to all Canadians.
Our team manufactures and markets a wide variety of pharmaceutical and health products that are distributed in pharmacies, healthcare practices and hospitals across the country.
At Bausch Health, we invest in our employees and we believe in the importance of cultivating performance and outdoing ourselves in finding new and better solutions with the aim of responding innovatively and effectively to current needs.
Scope
Act as a local PV contact person for local Health Authority
Act as a local PV contact person for audits and inspections and inform GPRM of incoming inspections/external audits
Establish, implement, and manage the MAH PV system, in accordance with relevant corporate procedures, Safety Data Exchange Agreements (SDEAs) and local regulations.
Ensure creation, maintenance and updates of local pharmacovigilance SOPs/WIs in according with local regulations and in line with Global SOPs
Oversight of local vendor/partner (s) conducting local PV activities
Key Activities / Responsibilities
Provide coordination and support for internal Pharmacovigilance activities
Ensure collection of drug safety information in the territory
Can participate in translation, reconciliation and follow-up if needed
Contribute to Aggregate Reports Team needs by:
o Acquiring data necessary for Aggregate reports preparation
o Contributing to Global Periodic Report schedule according to
authorizations/licenses in Canada
Implement, in conjunction with SDEA Team, local safety agreements with partners
Support review of local SDEAs and compliance (especially with local PV contractors) in cooperation with the global SDEA team
Maintain the Canadian list of products in the Company Product Dictionary
Monitor submission of Aggregate reports in collaboration with Regulatory Affairs
Liaise with Global and local functions for pharmacovigilance activities, as defined
Maintain the whole internal and external correspondence coming within her duties and activities and ensure relevant archiving of PV documentation if needed
Responsible for informing (in collaboration with GPRM team) Canadian Medical and Regulatory team about any safety issues in Canada
Support labelling safety update activities
Ensure local literature review and monitoring of the CanadaVigilance website is in place
Collaborate with Medical Affairs, Marketing, Regulatory Affairs and partners to refine the RMP and aRMMS strategies
Communicate any urgent safety issues to upper GPRM management
Ensure seamlessly integration of new acquisitions and divestments
Ensure safety updates and 72 hours notifications are submitted
Ensure local process for complaints/adverse events collection and reporting to GPRM is in place
Ensure inspection readiness
Manage or assist in management of PV audits and inspections from external regulatory agencies, partners or corporate auditors.
Participate in preparing responses to safety related requests from Health Authority
Establish local metrics and other monitoring systems to measure and verify local compliance
Prepare and manage local Non-Conformances/Deviations and CAPA
Participate in GPRM training activities and regular TCs
Organize PV training for local employees and local contract vendors
Perform Health Authority Website monitoring and inform GPRM of changes in local regulation pertaining to Pharmacovigilance
Ensure business continuity and back-up
Qualifications / Training
University degree with Pharmaceutical/Medical/Scientific background
Proven oral and written communication skills
Languages: excellent French and English skills
Technical knowledge of job-related systems
Knowledge of PV-related local regulations and understanding of International Pharmacovigilance regulations
Computing skills: user requiring advanced Literacy (Microsoft Office applications, Adobe Acrobat, Safety database)
A minimum of 8-10 years of relevant work experience in Pharmacovigilance
The masculine is used in this publication without prejudice for the sake of conciseness.
Bausch Health is committed to equal employment opportunity and complies with equal employment opportunity laws in effect wherever it operates.
Bausch Health is an EEO/AA employer M/F/D/V.