Quality & Compliance Manager — Life Sciences (Onsite)

CBRE; Indianapolis (IN); On-site; USD 70,000 - 100,000; Full time

Job summary

CBRE is seeking a Quality and Compliance Manager for a Life Sciences site in Lebanon, IN. This fully onsite role leads the QA/QC team, drives continuous improvement, and ensures program compliance. You will supervise staff, coordinate daily activities, and report metrics to stakeholders.

Required is a Bachelor's degree (preferred) with 3–5 years' relevant experience; licenses or certifications as required. Experience leading audits, CAPAs, and investigations in Life Sciences/Pharma/GMP is

Qualifications

• Bachelor's degree preferred with 3–5 years of relevant experience; license/certification where required.
• Experience leading audits, CAPAs, and investigations in Life Sciences/Pharma/GMP.
• Experience in staffing, training, development, coaching, mentoring, and performance management.
• Ability to communicate sensitive information clearly and guide performance expectations.

Responsibilities

• Provide formal supervision to employees; monitor training and performance evaluations.
• Coordinate and manage daily team activities; set schedules and deadlines.
• Execute compliance programs and participate in continuous improvement.
• Communicate initiatives and report compliance status to stakeholders.
• Monitor the success of quality initiatives for non-regulated services.
• Report metrics to client during review meetings and escalate issues.
• Lead inspection readiness programs and assist with audits.
• Model CBRE RISE values and influence stakeholders to reach agreements.
• Apply knowledge across disciplines to achieve objectives.
• Identify and resolve day-to-day and moderately complex issues.

Skills

Leadership

Coaching

Staffing

Communication

Problem solving

MS Office

Education

Bachelor's degree

Tools

Microsoft Office

Job description

CBRE is seeking a Quality and Compliance Manager for a Life Sciences site in Lebanon, IN. This fully onsite role leads the QA/QC team, drives continuous improvement, and ensures program compliance. You will supervise staff, coordinate daily activities, and report metrics to stakeholders.

Required is a Bachelor's degree (preferred) with 3–5 years' relevant experience; licenses or certifications as required. Experience leading audits, CAPAs, and investigations in Life Sciences/Pharma/GMP is