Senior Scientist, Analytical R&d

med-in.at

Base: $117,000.00 - $184,200.00; bonus/equity: ann...
Hybrid (3 days onsite, 1 day remote)
Late-stage method development and validation
Analytical technical transfer management
Cgmp laboratory environment experience
The Senior Scientist in Analytical R&D at med-in.at will oversee late-stage method development, validation, and lifecycle management for large molecule vaccines and biologics. The role requires collaboration across global teams, method transfers, and technical oversight of external testing labs, focusing on continuous improvement and compliance with regulatory standards

Job Summary

  • This role is accountable for the commercialization of large molecule, vaccines, and biologics from Phase III through launch and transfer to supply.
  • The position involves directing and managing analytical activities within a global network of contract manufacturing and testing organizations.
  • Candidates will receive a comprehensive benefits package including medical, dental, vision, 401(k), and paid holidays.

Matching Summary

Match Score: 85

The Senior Scientist in Analytical R&D at med-in.at will oversee late-stage method development, validation, and lifecycle management for large molecule vaccines and biologics. The role requires collaboration across global teams, method transfers, and technical oversight of external testing labs, focusing on continuous improvement and compliance with regulatory standards.

Salary

Base: $117,000.00 - $184,200.00; Bonus/Equity: Annual bonus and long-term incentive eligible; Benefits: Medical, dental, vision, 401(k), paid time off

Skills & Requirements

Must-have

  • Late-stage method development and validation
  • Analytical technical transfer management
  • cGMP laboratory environment experience
  • Large molecule biologics and vaccines
  • Assay life cycle activities
  • ICH USP compendial knowledge

Nice-to-have

  • Six Sigma and lean laboratory methodology
  • Global launch and supply experience
  • Regulatory filing support (BLA/MAA)
  • LIMS and software automation tools
  • Cross-functional stakeholder collaboration
  • Continuous improvement initiatives

Key Requirements

  • Bachelor's degree with 6 years industry experience
  • Master's degree with 4 years industry experience
  • PhD with 1 year industry experience
  • Minimum 2 years in cGMP large molecule labs
  • Experience with CMOs and CTLs preferred

Work Rights

Not specified

Tailored Resume

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