Associate Director, Technology Transfer Task Force

3 weeks ago


De Soto, United States Merck Full time

Associate Director, Technology Transfer Task Force – Animal Health Vaccines Join our Global Science & Technology Network leadership team to lead complex, site‑to‑site technology transfers for Animal Health vaccines across our U.S. manufacturing network. As Associate Director, you will own end‑to‑end execution for Large Molecule/Biologics transfers, ensuring on‑time, on‑budget delivery and compliant, unconstrained supply that supports business growth. You will provide strategic oversight, standardized methodology, and hands‑on leadership to transfer teams and site sponsors, while driving portfolio governance and alignment with our Network & Strategy Development Office. This role is based at a U.S. manufacturing site and focuses on transfers within the U.S. region. This is an opportunity to set standards, build capability, and grow our teams while delivering complex, strategic initiatives. Key Responsibilities Lead and support end‑to‑end site‑to‑site technology transfers for Animal Health vaccines (drug substance and drug product), from scoping/siting through PPQ and commercial readiness. Establish and deploy standardized transfer methodology, tools, training, and governance; ensure clear visualization of status through reporting and tiered escalation. Drive Block 1 scoping and siting assessments and, in collaboration with transfer lead, own timely execution of transfer strategies across Blocks 2–6, balancing speed, risk, and compliance. Serve as the single point of contact across donor and receiving sites and global functions; maintain tight stakeholder alignment and issue/risk management. Support engineering runs and PPQ; ensure strong process performance monitoring, deviation triage, CAPA effectiveness, and readiness for regulatory inspections. Build and develop high‑performing teams; coach transfer leads, allocate resources, and cultivate talent across a matrixed network. Required Qualifications Bachelor’s degree in Biotechnology, Chemical/biochemical Engineering, or a relevant science/business field. 5+ years of experience in vaccine or biologics manufacturing with a proven track record leading site‑to‑site technology transfers in Large Molecule operations. Demonstrated project management leadership delivering complex, multi‑site programs on time and within budget; PMP or equivalent experience preferred. Hands‑on expertise with pharmaceutical/biological processes (drug substance, drug product, formulation, fill‑finish, lyophilization; knowledge of single‑use systems, chromatography, filtration). People‑leadership experience: managing teams and influencing across matrixed organizations; coaching and developing transfer leads. Strong understanding of cGMP, PPQ, validation (process/cleaning/CSV), and global regulatory frameworks (USDA). Excellent verbal and written communication; effective negotiation and stakeholder management across sites and functions. Preferred Skills and Attributes Ability to manage multiple complex transfers simultaneously, maintain portfolio‑level visibility, and focus teams on critical‑path activities. Strong analytical judgment and risk‑based decision making; adept at fit‑to‑plant strategies, gap assessments, and mitigation planning. Proven capability working across cultures and time zones; strong networking skills within complex global organizations. Resilient, flexible, and calm under pressure; comfortable with aggressive timelines and changing priorities. Experience with digital tools supporting tech transfer and manufacturing (e.g., eQMS, MES, data historians, knowledge management). Willingness to travel as needed to donor/receiving sites within the U.S. Required Skills Analytical Thinking, Biologics, Communication, Drug Product Manufacturing, Leadership, Manufacturing, Project Management, Scoping, Technology Transfer, Vaccine Manufacturing, Work Collaboratively. Preferred Skills Experience with eQMS, MES, data historians, or knowledge management tools; willingness to travel; ability to manage complex, simultaneous projects. Salary $126,500.00 – $199,100.00 (base salary range). Travel Requirements 25% travel within the U.S. Flexible Work Arrangements Hybrid – 3 on‑site days per week, Monday‑Thursday; Friday remote work (subject to work‑critical tasks). EEO Statement As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other legally protected characteristic. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about your rights under U.S. EEO laws, visit EEOC Know Your Rights and EEOC GINA Supplement. We are proud to be a company that embraces diverse experiences, perspectives, skills and backgrounds. Learn more about your rights, including under California, Colorado and other U.S. state acts. U.S. Hybrid Work Model Effective September 5, 2023, employees in office‑based positions in the U.S. will be working a hybrid schedule consisting of three on‑site days per week, Monday‑Thursday, with Friday designated as a remote‑working day, unless business critical tasks require an on‑site presence. This hybrid work model does not apply to field‑based positions; facility‑based, manufacturing‑based, or research‑based positions where the work is located at a company site; positions covered by a collective‑bargaining agreement; or other positions for which the company determines the job requirements cannot be reasonably met working remotely. Location San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance.Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with applicable state and local laws including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Job Posting End Date 12/4/2025 #J-18808-Ljbffr



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