Starszy Kierownik / Starsza Kierowniczka Ds. Cyklu Życia Produktów B2b

Polpharma Group

Gdańsk, Poland
Hybrid or remote
B2b product lifecycle management
Cross-functional team coordination
Product change management
Polpharma Group is seeking a Senior Manager for B2B Product Lifecycle Management, responsible for overseeing product changes, coordinating cross-functional teams, and managing client relationships. The position offers a stable work environment with hybrid or remote options, competitive benefits, and opportunities for professional development

Job Summary

  • Manage the B2B product lifecycle, including out-licensing FDF, product changes, and their impact on production forecasts and supply continuity.
  • Coordinate cross-functional teams (Production, Quality, Supply Chain, Regulatory, Sales) and represent Polpharma B2B in client interactions.
  • The company offers stable employment, hybrid/remote work, private medical care, life insurance, Multisport card, annual bonus, and training opportunities.

Matching Summary

Match Score: 85

Polpharma Group is seeking a Senior Manager for B2B Product Lifecycle Management, responsible for overseeing product changes, coordinating cross-functional teams, and managing client relationships. The position offers a stable work environment with hybrid or remote options, competitive benefits, and opportunities for professional development.

Skills & Requirements

Must-have

  • B2B product lifecycle management
  • Cross-functional team coordination
  • Product change management
  • Supply chain management
  • cGMP and regulatory requirements
  • Project risk identification and mitigation
  • Client communication and representation

Nice-to-have

  • Experience in similar role
  • Teamwork and collaboration
  • Proactive and independent work

Key Requirements

  • Minimum 5 years of experience in the pharmaceutical industry
  • Higher education in pharmacy, chemistry, biology, medicine, or related fields
  • Strong leadership skills
  • Knowledge of pharmaceutical production requirements, cGMP, and regulatory procedures
  • Understanding of finished drug product manufacturing
  • Project management and risk assessment methodologies
  • Excellent English proficiency (min. C1)

Work Rights

Not specified

Tailored Resume

Cover Letter