Validation Manager

Life Science Professionals, LLC is dedicated to advancing excellence in the life sciences industry. With a strong focus on cGMP consulting and project management, the organization provides meticulous services to ensure client success. Recognized for building meaningful connections, we partner with professionals to support career growth and facilitate valuable opportunities within the life science community. Life Science Professionals is committed to delivering exceptional solutions while fostering excellence and innovation in life sciences.

This is a full-time on-site role for a Validation Manager located in Lake Forest, IL. The Validation Manager will oversee and execute validation processes, ensuring compliance with regulatory standards and company protocols. Day-to-day responsibilities include managing validation activities such as decommissioning, equipment qualification, process validation, and protocol development. Additional duties include creating and reviewing validation documentation, leading cross-functional teams, and troubleshooting technical issues to support continuous improvement in manufacturing or laboratory environments.

• Strong expertise in validation processes, including decommissioning, equipment qualification, process validation, and software validation
• Experience in drafting, reviewing, and managing validation documentation, such as protocols and reports
• Proficiency in cGMP standards and quality system regulations
• Excellent project management and organizational skills
• Strong analytical and problem-solving skills in troubleshooting validation and operational issues
• Effective communication and leadership skills to manage cross-functional teams and liaise with stakeholders
• Bachelor's degree in Engineering, Life Sciences, or related field; advanced degree or certifications in GMP/Validation practices is a plus
• Prior experience in the pharmaceutical, biotechnology, or medical device industry is highly desirable