Manager Manufacturing, Single Use Systems & Validation

• Provide technical leadership and subject matter expertise for Single Use Systems and equipment cleaning validation activities in the manufacturing area
• Oversee development, implementation, and maintenance of SOPs, training materials, and Quality Management System records related to Single Use Systems and equipment cleaning validation
• Lead development and execution of the site’s Cleaning Validation Master Plan (CIP/SIP/COP for equipment and controlled temperature chambers), validation plans, equipment qualification protocols/reports, and cleaning validation strategies
• Manage and mentor a team of specialists and engineers, including hiring, training, performance evaluations, and development
• Coordinate troubleshooting and support during commissioning, qualification, start-up, and process performance qualification of the facility
• Facilitate process, area, and equipment risk assessments to identify risks, failure modes, and mitigating actions
• Ensure compliance with regulatory requirements, support regulatory submissions, audits, and inspections
• Champion Lean Transformation and operational excellence initiatives, driving continuous improvement in the plant
• Collaborate cross-functionally with Manufacturing, Engineering, Quality, Supply Chain, and Process Development to ensure alignment and readiness for new products, process changes, and advanced technologies
• Develop and implement training plans and programs to ensure staff are prepared and compliant
• Maintain inspection readiness and support staff with audit or regulatory response strategy

• High school diploma/GED and 12 years of biotechnology operations or validation experience
• Associate’s degree and 10 years of biotechnology operations or validation experience
• Bachelor’s degree and 5 years of biotechnology operations or validation experience
• Master’s degree and 3 years of biotechnology operations or validation experience
• Doctorate degree

• Educational background in Chemical Engineering, Industrial Engineering, Biology, Biochemistry, Life Sciences, or related field
• Experience leading/managing a team of direct reports in a GMP manufacturing environment
• Strong technical knowledge of Single Use Systems and Cleaning Validation strategies for biologics manufacturing
• Experience in supporting regulatory submissions, audits, and inspections
• Proficient technical writing and presentation skills to communicate complex information effectively with technical and senior management staff
• Experience in cross-functional project management and operational excellence initiatives
• Ability to coach, mentor, and cross-train colleagues within core technical areas
• Background in lean manufacturing methodologies and continuous improvement
• Knowledge of relevant regulations (e.g., FDA Title 21 CFR Part 210/211, Eudralex Annex 15, ASTM E2500, ICH Q7)

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards