Sr. Scientist I - Microbiology

ALCAMI

Charleston, SC, US
Not specified; competitive salary offered; benefit...
On-site
Bachelor's degree in biology or microbiology
8+ years pharmaceutical or cdmo experience
Usp sterility testing and bioburden methods
Alcami is seeking a Sr. Scientist I in Microbiology to drive complex microbial analysis and assist in method development and validation in a fast-paced environment. The role requires extensive experience in aseptic manufacturing, microbial risk assessments, and strong communication skills, with a commitment to maintaining compliance with cGMP standards

Job Summary

  • The Sr. Scientist I will drive results by performing complex microbial analysis and assisting in method development within a fast-paced environment.
  • This role requires maintaining advanced knowledge of instrumentation and executing tasks according to standard operating procedures while ensuring GMP compliance.
  • Alcami offers a competitive salary, exceptional benefits including 401(k) with immediate vesting, and opportunities for professional growth in a collaborative team.

Matching Summary

Match Score: 85

Alcami is seeking a Sr. Scientist I in Microbiology to drive complex microbial analysis and assist in method development and validation in a fast-paced environment. The role requires extensive experience in aseptic manufacturing, microbial risk assessments, and strong communication skills, with a commitment to maintaining compliance with cGMP standards.

Salary

Not specified; Competitive salary offered; Benefits include medical, dental, vision, 401(k) match

Skills & Requirements

Must-have

  • Bachelor's degree in Biology or Microbiology
  • 8+ years pharmaceutical or CDMO experience
  • USP Sterility Testing and Bioburden methods
  • Aseptic manufacturing and ISO clean room operations
  • Steam and VHP sterilization process knowledge
  • GMP compliance and lab investigation participation

Nice-to-have

  • Method development and validation independence
  • Client technical contact experience
  • Corrective and preventative action leadership
  • Training and mentoring subordinate staff
  • Process improvement initiative participation

Key Requirements

  • Bachelor's degree required with 8+ years experience
  • Prior pharmaceutical or CDMO industry experience mandatory
  • Proficiency in USP <61>, <62>, <71>, <85> methods
  • Strong knowledge of cGMP regulations
  • Excellent verbal and written communication skills

Work Rights

Not specified

Tailored Resume

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