Environmental QC Associate – EM Monitoring (Swing Shift)

Capricor Therapeutics

California

Sur place

USD 65 000 - 85 000

Plein temps

Il y a 2 jours

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Avantages offerts par ce poste

Discretionary bonus

Equity incentives

Medical insurance

401(k) match

Paid time off

Parental leave

Résumé du poste

Capricor Therapeutics is seeking a Quality Control Associate for Environmental Monitoring (EM) to maintain GMP-compliant environmental conditions in controlled areas. You will perform air, surface, water sampling, data trending, and investigations, working with QC, QA, and Production to uphold a state of control.

The role requires a Life Sciences degree and 2–5 years of EM/quality control experience in regulated environments.

Qualifications

Bachelor’s degree in Life Sciences, Chemistry, Microbiology, or a related field.
2–5 years of experience in environmental monitoring or quality control within a regulated environment.
Knowledge of GMP, ISO, FDA expectations, and environmental monitoring standards.
Experience performing environmental sampling and handling EM equipment.
Strong documentation, data integrity, and analytical skills.
Ability to work effectively in controlled environments, including cleanrooms.
Strong organizational and time‑management skills for handling multiple priorities.

Responsabilités

Conduct routine environmental monitoring in controlled and classified areas in alignment with GMP, ISO, and regulatory requirements.
Perform sampling of air, surfaces, water, and equipment using approved methods.
Document sampling activities and results accurately in accordance with GMP and data integrity standards.
Analyze environmental monitoring data to identify trends, excursions, and required corrective or preventive actions.
Escalate atypical results promptly and support the investigation, documentation, and closure of deviations and CAPAs.
Maintain calibration, readiness, and routine upkeep of environmental monitoring equipment.
Support audit and inspection readiness through compliant documentation and area oversight.
Collaborate with QC, QA, and Production to address findings, implement improvements, and maintain a state of control.
Follow gowning and cleanroom entry procedures consistently and perform duties in full cleanroom attire.
Participate in continual learning, safety programs, and ongoing process improvements.