Eagle Analytical Services
Associate Director of Engineering
Eagle Analytical Services, Houston, Texas, United States, 77246
Associate Director of Engineering
The Associate Director of Engineering is responsible for the development and direction of new ventures requiring all aspects of process engineering, supporting both internal laboratory operations and external client projects. This individual serves as a technical lead and subject matter expert (SME) for engineering-based consulting services and is expected to contribute to proposals, delegate project tasks, lead protocol authorship and execution, and ensure on-time, audit-ready deliverables. Strong communication, project management, and technical writing skills are essential. What You Will Do Provide scientific and business leadership to ensure departmental performance meets customer expectations and business goals in cost, quality, and turnaround time. Drive efficiency and cost-effectiveness within analytical chemistry and microbiology laboratories. Serve as a technical escalation point for complex qualification, validation, and facilities-related challenges. Apply scientific and engineering principles to develop practical, economical solutions to technical problems. Oversee mechanical and electrical aspects of engineering designs by Architect-Engineer firms for systems and facilities, including ISO-certified cleanrooms and HVAC systems. Ensure compliance with CGMP regulations, internal SOPs, and equipment lifecycle best practices. Lead staff selection, development, and performance management for the Engineering team. Develop and execute IQ, OQ, and PQ protocols for laboratory equipment in compliance with GDP guidelines and internal quality standards. Troubleshoot and investigate equipment and system issues. Lead client-facing projects involving facility assessments, equipment and utility qualification, process and cleaning validation, environmental system design review, and certification readiness. Analyze and interpret data, technical drawings, manuals, and schematics to resolve laboratory and facility issues. Partner with executive leadership and cross-functional teams to support strategic initiatives. Ensure facilities operate safely and comply with all federal, state, and local codes/regulations. Maintain compliance with DEA, FDA, and Texas Department of Public Safety requirements. Support investigations, deviation management, and CAPA development related to engineering systems and equipment failures. Plan, execute, and document engineering workstreams effectively. Manage independent projects for internal and external clients. Travel up to 30% to support client engagements and site operations. Who You Are Bachelor's degree in mechanical engineering, chemical engineering, or electrical engineering; MS preferred. Ten years' engineering experience (15 preferred). Five years of demonstrated knowledge of Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) specific to Validation of Analytical methods. Strong technical expertise in cleanroom certification standards, utility qualification, equipment lifecycle management and IQ/OQ/PQ execution, process validation, and change control systems. Excellent analytical and interpersonal skills. Excellent verbal and written communication skills. Advanced level computer skills. Advanced technical degree, a plus. Certifications PE preferred Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
The Associate Director of Engineering is responsible for the development and direction of new ventures requiring all aspects of process engineering, supporting both internal laboratory operations and external client projects. This individual serves as a technical lead and subject matter expert (SME) for engineering-based consulting services and is expected to contribute to proposals, delegate project tasks, lead protocol authorship and execution, and ensure on-time, audit-ready deliverables. Strong communication, project management, and technical writing skills are essential. What You Will Do Provide scientific and business leadership to ensure departmental performance meets customer expectations and business goals in cost, quality, and turnaround time. Drive efficiency and cost-effectiveness within analytical chemistry and microbiology laboratories. Serve as a technical escalation point for complex qualification, validation, and facilities-related challenges. Apply scientific and engineering principles to develop practical, economical solutions to technical problems. Oversee mechanical and electrical aspects of engineering designs by Architect-Engineer firms for systems and facilities, including ISO-certified cleanrooms and HVAC systems. Ensure compliance with CGMP regulations, internal SOPs, and equipment lifecycle best practices. Lead staff selection, development, and performance management for the Engineering team. Develop and execute IQ, OQ, and PQ protocols for laboratory equipment in compliance with GDP guidelines and internal quality standards. Troubleshoot and investigate equipment and system issues. Lead client-facing projects involving facility assessments, equipment and utility qualification, process and cleaning validation, environmental system design review, and certification readiness. Analyze and interpret data, technical drawings, manuals, and schematics to resolve laboratory and facility issues. Partner with executive leadership and cross-functional teams to support strategic initiatives. Ensure facilities operate safely and comply with all federal, state, and local codes/regulations. Maintain compliance with DEA, FDA, and Texas Department of Public Safety requirements. Support investigations, deviation management, and CAPA development related to engineering systems and equipment failures. Plan, execute, and document engineering workstreams effectively. Manage independent projects for internal and external clients. Travel up to 30% to support client engagements and site operations. Who You Are Bachelor's degree in mechanical engineering, chemical engineering, or electrical engineering; MS preferred. Ten years' engineering experience (15 preferred). Five years of demonstrated knowledge of Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA) specific to Validation of Analytical methods. Strong technical expertise in cleanroom certification standards, utility qualification, equipment lifecycle management and IQ/OQ/PQ execution, process validation, and change control systems. Excellent analytical and interpersonal skills. Excellent verbal and written communication skills. Advanced level computer skills. Advanced technical degree, a plus. Certifications PE preferred Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.