V

Viatris

Global pharma selling generics and biosimilars

Senior Manager PV Sweden & Affiliate Safety Representative

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSolna, SwedenNo salary listedIn-person

About the Job

Requirements

  • A medical, pharmacy, or life-sciences degree, or equivalent, is required.
  • At least three years of experience in the pharmaceutical industry and at least two years of pharmacovigilance experience are required.
  • Management and leadership skills and a high level of autonomy are required.
  • The candidate must demonstrate the ability to deliver quality work using organizational, facilitation, and interpersonal skills in cross-functional teams locally, within pharmacovigilance, and externally.
  • Experience working in cross-functional teams and/or global projects, including teamwork and virtual collaboration, is required.
  • Excellent written and spoken English and Swedish are required.
  • Analytical ability and attention to detail are required.
  • Knowledge of European and Swedish pharmacovigilance regulations is required.
  • Technical writing and authoring skills, including standard operating procedures and procedural documents, corrective action plans, and exception reports, are required.

Responsibilities

  • Organize, manage, and maintain a highly compliant pharmacovigilance system for Viatris in Sweden.
  • Maintain awareness of and ensure adherence to established and updated local and global processes and guidelines, and national and international pharmacovigilance regulations and guidelines.
  • Lead, supervise, and coordinate PV team members and PV-related external service providers in Sweden.
  • Ensure pharmacovigilance business continuity.
  • Serve as the main contact point for Swedish health authorities regarding pharmacovigilance matters and inspections.
  • Lead and coordinate internal and external pharmacovigilance audits and inspections.
  • Monitor affiliate pharmacovigilance system performance and compliance.
  • Plan and manage the local pharmacovigilance budget.
  • Oversee day-to-day pharmacovigilance activities, including individual case safety report management, cooperation on PSUR submissions, archiving, implementation of local risk-minimization measures, management and fulfillment of pharmacovigilance agreements, maintenance of updated local standard operating procedures aligned with global processes and applicable regulations, and training of affiliate employees and service providers as applicable.
  • Cooperate with global pharmacovigilance teams as requested or needed.

Desired Qualifications

  • Knowledge of cosmetovigilance, medical device vigilance, and food-supplement vigilance is strongly recommended.
  • Good knowledge of other international pharmacovigilance regulations and relevant legislation, including ICH and CIOMS, is strongly recommended.

About the Company

Viatris

Global pharma selling generics and biosimilars

Viatris is a global pharmaceutical company that provides access to medicines through a diverse portfolio of branded drugs, generics, complex generics, and biosimilars, serving patients in more than 165 countries. Medicines are produced and distributed via Viatris's extensive global supply chain and commercial network, making therapies available across cardiovascular, infectious diseases, immunology, and oncology. The company differentiates itself with a large, diversified product mix, broad international reach, and a focus on access and public health rooted in the Mylan-Upjohn lineage. Its strategy combines organic growth with partnerships and acquisitions to expand patient access while pursuing sustainable operations.

Company size
10,001+
Company stage
IPO
Headquarters
Canonsburg, PA
Founded
1961

Recently Posted Jobs

Explore more opportunities at Viatris

See more jobs