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Environmental Monitoring - QC Analyst III

Astrix Technology

Wilmington, OHFull-timeNo compensation foundTracked 3w agoSeen in employer's feed 1w ago

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At a glance

Compensation
No compensation found
Location
Wilmington, OH
Schedule
Full-time
Work Authorization
Not specified

Job overview

Astrix Technology is hiring an Environmental Monitoring - QC Analyst III. A top‑performing pharmaceutical manufacturer seeks a QC Analyst III – Environmental Monitoring to work in a sterile manufacturing environment, impacting product quality, patient safety, and operational excellence while collaborating with a supportive Quality Control team.

Key focus areas include Perform routine, batch‑related, and quarterly environmental monitoring in aseptic, classified, and controlled manufacturing areas, Collect environmental monitoring samples in cleanroom environments, and Support sterile manufacturing operations through production observations and cleanroom walkthroughs.

Important skills include Environmental Monitoring, Cleanroom Sampling, Utilities Sampling, Utilities Testing, Endotoxin Testing, and Bioburden Testing. Preferred (not required): Aseptic Techniques, Contamination Control Strategies, Microbiological Testing, and TOC Testing.

Skills & qualifications

RequiredNice to have

Skills

Environmental MonitoringCleanroom SamplingUtilities SamplingUtilities TestingEndotoxin TestingBioburden TestingAseptic GowningSterile Gowning QualificationWater SystemsCompressed GasesAseptic TechniquesContamination Control StrategiesMicrobiological TestingTOC TestingConductivity TestingSOPsRisk AssessmentsChange ControlsProtocolsTechnical ReportsInvestigationsDeviationsCorrective ActionsGMP RequirementsTrainingCoachingTechnical Resource

Qualifications

4+ Years Pharmaceutical Microbiology Experience4+ Years QC Experience4+ Years Environmental Monitoring ExperienceExperience Supporting Sterile Manufacturing OperationsBachelor's Degree in BiologyBachelor's Degree in MicrobiologyBachelor's Degree in Life SciencesBachelor's Degree in Related Scientific Discipline

Full job description

Environmental Monitoring - QC Analyst III

Quality Control

Wilmington, Ohio, US

  • Added - 04/08/2026

Pay Rate Low: 70000 | Pay Rate High: 90000

QC Analyst III – Environmental Monitoring (EM)

_Relocation Assistance Available!_

Location: Dayton, OH

Schedule: Monday–Friday | 8:00 AM – 5 PM

Employment Type: Perm Hire, Full-Time

Salary: $70,000 – $90,000 + Annual Bonus

About the Opportunity

A top-performing pharmaceutical manufacturer recognized for its exceptional workplace culture, is seeking a QC Analyst III – Environmental Monitoring (EM) to join its Quality Control team. This is a unique opportunity to work in a sterile manufacturing environment where you'll have a direct impact on product quality, patient safety, and operational excellence while partnering with a highly collaborative and supportive team!

Key Responsibilities

Environmental Monitoring

  • Perform routine, batch-related, and quarterly environmental monitoring in aseptic, classified, and controlled manufacturing areas.

  • Collect environmental monitoring samples in cleanroom environments.

  • Support sterile manufacturing operations through production observations and cleanroom walkthroughs.

  • Monitor compliance with aseptic techniques and contamination control strategies.

Utilities Monitoring & Testing

  • Perform utilities sampling and testing of:

  • Water for Injection (WFI)

  • Purified Water (PW)

  • Potable/City Water

  • Compressed Air

  • Nitrogen and other process gases

  • Conduct microbiological testing including:

  • Endotoxin (Required)

  • Bioburden (Required)

  • TOC (Preferred)

  • Conductivity (Preferred)

  • Enumerate organisms from environmental and utility samples.

Quality Systems & Documentation

  • Author, revise, and maintain:

  • SOPs

  • Risk Assessments

  • Change Controls

  • Protocols

  • Technical Reports

  • Support investigations, deviations, and corrective actions.

  • Review technical documentation from internal stakeholders.

  • Maintain documentation in accordance with GMP requirements.

Training & Technical Leadership

  • Train manufacturing and environmental monitoring personnel

  • Support gowning qualifications and annual requalification activities.

  • Mentor junior team members and serve as a technical resource within the department.

  • Represent the department during meetings, audits, and cross-functional initiatives.

Required Qualifications

  • Bachelor's Degree in Biology, Microbiology, Life Sciences, or a related scientific discipline preferred.

  • 4+ years of pharmaceutical microbiology, QC, or Environmental Monitoring experience.

  • Experience supporting sterile manufacturing operations.

  • Environmental Monitoring (EM) and cleanroom sampling experience.

  • Aseptic gowning and sterile gowning qualification experience.

  • Utilities sampling and testing experience.

  • Required: Endotoxin and Bioburden testing.

  • Experience with water systems (WFI, Purified Water, Potable Water) and compressed gases (air and nitrogen).

This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

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We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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