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Director, Pharmacovigilance
Director, PharmacovigilanceBausch & Lomb • Laval, Canada
Director, Pharmacovigilance

Director, Pharmacovigilance

Bausch & Lomb • Laval, Canada
Il y a plus de 30 jours
Type de contrat
  • Temps plein
Description de poste

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.

This is a hybrid position with two days of remote work and three days at our head office in Laval.

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.

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