2nd Shift Environmental Compliance Lead — EM & QA Oversight

Kindeva-Drug-Delivery-Careers; Brentwood (MO); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Competitive base salary

Performance bonus

Comprehensive benefits

Job summary

Kindeva-Drug-Delivery-Careers in Brentwood, MO seeks an Environmental Compliance Supervisor to lead EM technicians and oversee EM programs for 24/7 manufacturing operations. The role emphasizes investigations, CAPA, and regulatory readiness in a fast-paced CDMO biopharmaceutical setting.

The candidate should have a strong background in environmental monitoring, data integrity, and quality systems, with leadership experience and a passion for continuous improvement.

Qualifications

• Bachelor’s degree in a scientific discipline (Microbiology/Biology/Pharmaceutical Sciences) preferred.
• 3–5 years in QC, Microbiology, Environmental Monitoring, or QA systems in pharma/biotech.
• 1–3 years of leadership within EM or pharma manufacturing preferred.
• Experience with regulatory inspections and CAPAs.

Responsibilities

• Lead a team of environmental monitoring technicians to support 24/7 manufacturing operations.
• Oversee EM data review, investigations, CAPA actions, and change controls.
• Collaborate with QA and manufacturing to ensure regulatory inspection readiness.
• Review EM and water system trends for risk assessment and remediation.
• Manage MODA Environmental Monitoring program updates and workflow improvements.
• Support investigations for EM excursions, OOS/OOT/OOE, deviations.
• Assist with documentation, audits, and regulatory responses.

Skills

Leadership

Environmental Monitoring

Data Integrity

Investigations

CAPA

Change Control

Regulatory Inspections

Quality Systems

Risk Assessment

Cross-functional Collaboration

Education

Bachelor’s Degree in Microbiology/Biology/Pharmaceutical Sciences

Tools

MODA EM Systems

LIMS

Electronic Quality Systems

Job description

Kindeva-Drug-Delivery-Careers in Brentwood, MO seeks an Environmental Compliance Supervisor to lead EM technicians and oversee EM programs for 24/7 manufacturing operations. The role emphasizes investigations, CAPA, and regulatory readiness in a fast-paced CDMO biopharmaceutical setting.

The candidate should have a strong background in environmental monitoring, data integrity, and quality systems, with leadership experience and a passion for continuous improvement.