Mgr., Biologics External Mfg. Quality (Hybrid)
The position collaborates with supply chain, technical operations, and CMC Program Management to review and support approval of deviations, change controls, batch records, validation protocols, quality agreements, and regulatory documentation. The Manager assists with batch disposition and supports external audit activities.
Essential Functions:
- Review and approve batch records for DS and DP manufacturing, ensuring compliance and data integrity.
- Assess and approve deviations, investigations, and CAPAs related to DS and DP operations (e.g., EM excursions, media fill failures, process deviations).
- Oversee change controls impacting DS and DP processes.
- Support batch disposition activities to ensure timely and complaint product release.
- Monitor and track manufacturing data for integrity and compliance.
- Ensure CMO compliance with quality systems (change control, deviations, investigations, OOS results, validation, retain sample management).
- Contribute to evaluation of product complaints and regulatory compliance of CMOs.
- Review technical protocols, reports, batch records, and regulatory documentation related to DS and DP manufacturing and validation activities.
- Support development and maintenance of processes and procedures governing quality systems and CMO interactions.
- Collaborate with internal and external stakeholders to drive compliance, continuous improvement and risk mitigation across external manufacturing operations.
- Education: BS/BA in life sciences or engineering (required); advanced degree desirable.
- Experience: 5+ years of Quality experience in biologics DS and DP operations, including aseptic fill-finish.
- Knowledge of EU GMP Annex 1 & Annex 2, FDA aseptic guidance, and global sterility assurance principles.
- Experience with DS processes (cell culture, purification) and DP aseptic operations (media fills, EM trending, contamination control strategies)
- Understanding of Quality System Management (lot disposition, deviations, change management, complaints).
- Strong organizational and communication skills; ability to manage multiple priorities.
- Proficiency in Microsoft Office tools.
- Ability to travel up to 25% (domestic and international).
- Required onsite Tuesday-Thursday
The annual base salary range for the Mgr., Biologics External Mfg. Quality (Hybrid) is from :$104,800-$137,600 Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan. Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills. Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit . Certain other benefits may be available for this position, please discuss any questions with your recruiter. Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans. Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information: Right To Work E-Verify Participation
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