Senior PV Third-Party Strategy & Oversight Lead

Bristol-Myers Squibb

Poland

On-site

PLN 120,000 - 170,000

Full time

9 days ago
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Job summary

Bristol Myers Squibb in Poland is seeking a Senior Manager, Third Party Strategy and Oversight (TPSO) to lead external PV oversight within Safety Quality Management. You will ensure compliance with global pharmacovigilance regulations, internal standards, and contract requirements while guiding governance across third‑party portfolios.

You will partner with cross‑functional teams to monitor performance, manage issues, and drive continuous improvement.

Qualifications

  • Bachelor's degree in Life Sciences or related discipline; advanced degree preferred.
  • 5-7 years in Pharmacovigilance, Safety Operations, Quality, or other regulated pharmaceutical functions.
  • Experience supporting third‑party oversight, governance processes, and compliance frameworks in a global pharmaceutical environment.
  • Knowledge of global PV regulations, GxP expectations, and quality systems.
  • Strong analytical and organisational skills; effective communication and cross‑functional collaboration.

Responsibilities

  • Support third‑party governance framework and oversight standards across global PS engagements.
  • Execute oversight activities across portfolios, including compliance monitoring, performance reviews, and issue management.
  • Monitor third‑party compliance metrics and identify trends, risks, and areas for improvement.
  • Assist in investigation and documentation of compliance issues, including CAPAs and root cause analysis.
  • Collaborate with stakeholders to support inspection readiness, audits, and responses to findings.

Skills

Analytical skills
Organisational skills
Communication skills
Problem-solving
Accountability & quality mindset

Education

Bachelor's degree in Life Sciences, Pharmacy, Nursing, Public Health, or related discipline

Job description

Bristol Myers Squibb in Poland is seeking a Senior Manager, Third Party Strategy and Oversight (TPSO) to lead external PV oversight within Safety Quality Management. You will ensure compliance with global pharmacovigilance regulations, internal standards, and contract requirements while guiding governance across third‑party portfolios.

You will partner with cross‑functional teams to monitor performance, manage issues, and drive continuous improvement.

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