Project Manager, Cmc Regulatory Affairs

Gsicareers

Unknown
Base: $113,850 to $189,750 (us); pln 236,250 to pl...
Hybrid
Cmc regulatory submission preparation
Cross-functional matrix project teams
Regulatory compliance maintenance
GSK aims to positively impact the health of 2.5 billion people by the end of the decade through innovative vaccines and medicines

Job Summary

  • GSK aims to positively impact the health of 2.5 billion people by the end of the decade through innovative vaccines and medicines.
  • The role involves responsibility for global CMC regulatory activities including strategy development, submission documents, and cross-functional collaboration.
  • Employees benefit from attractive reward packages, hybrid working models, extensive work-life balance support, and personalized learning opportunities.

Matching Summary

GSK aims to positively impact the health of 2.5 billion people by the end of the decade through innovative vaccines and medicines.

Salary

Base: $113,850 to $189,750 (US); PLN 236,250 to PLN 393,750 (Poland); Bonus/Equity: Annual bonus and share-based long term incentive program; Benefits: Health care, insurance, retirement, paid leave, private medical package, sports cards

Skills & Requirements

Must-have

  • CMC regulatory submission preparation
  • cross-functional matrix project teams
  • regulatory compliance maintenance
  • drug development and manufacturing knowledge
  • project management across all phases

Nice-to-have

  • continuous improvement and innovation
  • supportive community and integration events
  • personalized learning and mentoring
  • hybrid working model
  • effective time management skills

Key Requirements

  • Degree in life sciences or related discipline
  • Experience in CMC regulatory affairs or product development
  • Knowledge of worldwide CMC regulatory requirements
  • Strong theoretical project management knowledge
  • Ability to manage multiple priorities and tight deadlines

Work Rights

Not specified

Tailored Resume

Cover Letter