Environmental Microbiology Compliance Lead

Kindeva

Brentwood (MO)

On-site

USD 90,000 - 140,000

Full time

14 days+
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Benefits offered by this job

Competitive base salary
Performance bonus
401k
Mentorship and professional dev

Job summary

Kindeva is seeking an Environmental Compliance and Microbiology Technical Specialist to join our St. Louis area team.

You will lead microbiological quality systems, environmental monitoring, and data integrity programs across QC operations, supporting CAPAs, investigations, and inspection readiness. The role requires a strong scientific background, 3–5 years in pharma/biotech QC, and experience with regulatory inspections, EM, and water systems.

Qualifications

  • Bachelor’s degree in a relevant scientific discipline.
  • 3–5 years in Quality Control, Microbiology, Environmental Monitoring, or related QC roles in pharma/biotech/CDMO.
  • Experience with investigations, CAPAs, change controls, inspections, audits, and sterile parenteral manufacturing.

Responsibilities

  • Serve as site SME for microbiological compliance and EM systems.
  • Support investigations, CAPA development, EM oversight, and trend analysis.
  • Ensure EM and water systems stay within state of control and compliant with global regulations.
  • Lead or support regulatory inspections and supplier validations as needed.
  • Review data integrity, GDP, and cGMP practices across QC and environmental programs.
  • Collaborate cross-functionally to implement improvements in EM and contamination control.

Skills

Environmental Monitoring
Data Integrity
Investigations
CAPA
Quality Systems
Regulatory Inspections
Scientific Judgement

Education

Bachelor's degree in Microbiology/Biology/Biotechnology/Pharmaceutical Sciences/Biochemistry

Job description

Kindeva is seeking an Environmental Compliance and Microbiology Technical Specialist to join our St. Louis area team.

You will lead microbiological quality systems, environmental monitoring, and data integrity programs across QC operations, supporting CAPAs, investigations, and inspection readiness. The role requires a strong scientific background, 3–5 years in pharma/biotech QC, and experience with regulatory inspections, EM, and water systems.

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