Experienced Quality and Compliance Director – Life Sciences Industry Leader in Regulatory Compliance and Quality Management

Introduction to CBRE and the Life Sciences Industry

Congratulations on considering a career move that could be the most rewarding of your professional life! We are CBRE, a global leader in managing highly-regulated spaces within the life sciences industry, including pharmaceuticals, biotech, medical devices, and genomics. Our comprehensive range of services includes laboratory consulting, real estate services, instrumentation repair and maintenance, full asset management, and more. With expertise across various life sciences categories, we are committed to delivering exceptional quality and compliance solutions to our clients.

About the Role of Quality and Compliance Director

We are seeking an experienced Quality and Compliance Director to lead our team of Quality Representatives on large scoped client accounts. This role may also involve leading corporate QA departments, facilitating company QA and Compliance objectives, and cascading these objectives to client accounts. As a Quality and Compliance Director, you will be responsible for managing staff responsible for creating, implementing, and maintaining Quality Management Systems (QMS) for CBRE and our clients. Your expertise will ensure the delivery of all quality and compliance deliverables for regulated and non-regulated services provided to our clients.

Key Responsibilities

• Lead the CBRE Quality Representatives staff on large scoped client accounts, ensuring the creation, implementation, and routine maintenance of QMS.
• Manage staff responsible for the inspection readiness program, vendor management program, and quality auditing.
• Oversee the development and implementation of quality initiatives, ensuring alignment with current regulatory body requirements.
• Interface with CBRE and client leadership teams, communicating quality and compliance initiatives and issues across functional areas.
• Author and negotiate terms of Quality Agreements with clients and vendors, ensuring GxP compliance and qualification of all regulated service vendors.
• Investigate deviations/events, manage Corrective/Preventative Actions, and participate in creation and management of changes.

Essential Qualifications

• Bachelor's degree in Biology, Microbiology, Chemistry, or Engineering; or equivalent related work experience.
• Minimum of 8-10 years of experience in a pharmaceutical research/manufacturing quality organization, with previous departmental experience required.
• FDA, ISO, or similar quality assurance audit-related certification preferred.
• Green or Black Belt Six Sigma Certification preferred.
• Excellent communication skills, with the ability to comprehend, analyze, and interpret complex business documents.
• In-depth knowledge of financial terms and principles, with the ability to calculate complex figures and forecast budgets.

Preferred Qualifications

• Experience with lean manufacturing, Six Sigma, 5S programs, and other quality management systems.
• Previous oversight of training and qualification programs within a regulated environment.
• Quality auditing experience, with expertise in Quality and Compliance management systems within Life Science Environment(s).
• Experience with Desktop publishing, Microsoft Office Suite, and Online Help, as well as SAP, Trackwise, Regulus, and/or CMMS systems.

Career Growth Opportunities and Learning Benefits

At CBRE, we are committed to the growth and development of our employees. As a Quality and Compliance Director, you will have access to a range of training and development opportunities, including formal training programs, mentorship, and coaching. You will also have the opportunity to work with a talented team of professionals who are passionate about delivering exceptional quality and compliance solutions to our clients.

Work Environment and Company Culture

Our company culture is built on a foundation of integrity, respect, and excellence. We value diversity and inclusion, and we are committed to providing a work environment that is collaborative, supportive, and empowering. As a Quality and Compliance Director, you will be working in a remote office, with the opportunity to collaborate with colleagues and clients across the continental USA.

Compensation, Perks, and Benefits

We offer a competitive salary range of $170,000 to $180,000 annually, depending on experience and qualifications. Our comprehensive benefits package includes health, vision, and life insurance, 401k, and personal time off, among others. We also offer a range of perks and benefits, including flexible working arrangements, professional development opportunities, and a dynamic and supportive work environment.

Conclusion

If you are a motivated and experienced quality and compliance professional looking for a new challenge, we encourage you to apply for this exciting opportunity. As a Quality and Compliance Director at CBRE, you will have the opportunity to make a significant impact on our business and our clients, while developing your skills and expertise in a dynamic and supportive environment. Don't miss out on this opportunity to take your career to the next level – apply now and join our team of talented professionals!

How to Apply

To apply for this role, please submit your application through our website. We look forward to receiving your application and exploring how you can contribute to our team's success.