Senior Scientist, Analytical R&d

539

Base: $117,000.00 - $184,200.00; bonus/equity: ann...
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Late-stage method development and validation
Large molecule biologics and vaccines experience
Cgmp laboratory environment knowledge
** The Senior Scientist position at 539 focuses on overseeing late-stage method development, validation, and analytical transfer for large molecules, vaccines, and biologics. The ideal candidate will have extensive experience in analytical techniques within a biopharmaceutical setting and will be responsible for collaborating with internal and external teams to drive continuous improvement and ensure 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 supply transfer.
  • The position involves directing analytical activities within a global network of external manufacturing and testing sites to support on-time batch release.
  • Candidates will work in a hybrid model requiring three days on-site per week and are eligible for an annual bonus and comprehensive benefits package.

Matching Summary

Match Score: 75

** The Senior Scientist position at 539 focuses on overseeing late-stage method development, validation, and analytical transfer for large molecules, vaccines, and biologics. The ideal candidate will have extensive experience in analytical techniques within a biopharmaceutical setting and will be responsible for collaborating with internal and external teams to drive continuous improvement and ensure 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 holidays

Skills & Requirements

Must-have

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

Nice-to-have

  • Six Sigma and lean laboratory methodology
  • Experience with CMOs and contract testing labs
  • Regulatory filing support (BLA, IND)
  • Cross-functional stakeholder collaboration
  • Data trending and continuous improvement

Key Requirements

  • Bachelor's degree plus 6 years industry experience OR Master's plus 4 years OR PhD plus 1 year
  • Minimum two years in cGMP large molecule environment
  • US residency required (US and Puerto Rico Residents Only)

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter