Principal Scientist, Method Development & validation

Bachem

Base: $131,246 - $180,463; bonus: annual performan...
On-site
15+ years industry experience in chemistry
Extensive hplc uplc lc-ms gc-ms expertise
Gmp environment experience required
Bachem is seeking a Principal Scientist for Method Development & Validation to oversee analytical methods for peptide drug substances and raw materials in a GMP environment. The ideal candidate will have extensive experience in method development and a strong background in analytical instrumentation

Job Summary

  • This role guides the development of release, stability, and in-process analytical methods for peptide drug substances and finished products.
  • The successful candidate will independently design advanced analytical methods using techniques such as HPLC, UPLC, LC-MS, and GC-MS.
  • Bachem offers a competitive total rewards package including annual performance bonuses, comprehensive medical coverage, and a 401(k) plan with employer contribution.

Matching Summary

Match Score: 85

Bachem is seeking a Principal Scientist for Method Development & Validation to oversee analytical methods for peptide drug substances and raw materials in a GMP environment. The ideal candidate will have extensive experience in method development and a strong background in analytical instrumentation.

Salary

Base: $131,246 - $180,463; Bonus: Annual performance bonus included; Benefits: Medical/Dental/Vision, 401(k), paid vacation

Skills & Requirements

Must-have

  • 15+ years industry experience in chemistry
  • Extensive HPLC UPLC LC-MS GC-MS expertise
  • GMP environment experience required
  • Independent method development and validation
  • Technical leadership and training capabilities

Nice-to-have

  • Peptide characterization experience preferred
  • Master Control or Veeva software knowledge
  • Innovation project implementation experience
  • Strong written and oral communication skills

Key Requirements

  • B.S./M.S. with 15+ years experience or Ph.D. with 12+ years
  • 3+ years GMP environment experience
  • 10+ years Method Development & Validation experience
  • 10+ years ICH FDA USP GMP standards knowledge
  • 7+ years Technical Leadership experience

Work Rights

Not specified

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