Environmental Compliance Lead, 2nd Shift

Kindeva Drug Delivery; Missouri; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive base salary + bonus

Comprehensive benefits package

Mentorship & professional development

Exposure to cutting-edge tech

Clear career progression to senior','

Collaborative work culture

Job summary

Kindeva Drug Delivery in Brentwood, MO operates on a 2nd shift (2:00 PM–10:30 PM) leading environmental monitoring and quality systems to ensure 24/7 manufacturing readiness. The EC Supervisor provides oversight for EM programs, contamination control, and regulatory-aligned investigations while supporting CAPA and change controls.

The role requires collaboration across QC/QA and manufacturing teams, with a focus on data integrity, GDP, ALCOA+ principles, and inspection readiness.

Qualifications

• Bachelor’s Degree in Microbiology, Biology, Biotechnology, Pharmaceutical Sciences, Biochemistry, or related discipline preferred.

Responsibilities

• Lead a team of environmental monitoring technicians to support 24/7 manufacturing operations.
• Collaborate with EC supervisors to ensure timely completion of sampling and documentation.
• Oversee EM data review, data integrity, ALCOA+ and GDP adherence.
• Assist with CAPA actions, change controls, and regulatory inspection readiness.
• Partner with QA and leadership to communicate production and monitoring needs.

Skills

Leadership

Attention to detail

Investigations

Communication

Quality systems

Risk assessment

Troubleshooting

Cross-functional collaboration

Education

Bachelor’s degree in Microbiology/related

Tools

MODA EM Systems

LIMS

Electronic Quality Systems

Audit trail review

Job description

Kindeva Drug Delivery in Brentwood, MO operates on a 2nd shift (2:00 PM–10:30 PM) leading environmental monitoring and quality systems to ensure 24/7 manufacturing readiness. The EC Supervisor provides oversight for EM programs, contamination control, and regulatory-aligned investigations while supporting CAPA and change controls.

The role requires collaboration across QC/QA and manufacturing teams, with a focus on data integrity, GDP, ALCOA+ principles, and inspection readiness.