Alexion Pharmaceuticals, Inc. · 15 hours ago
Associate Director, Injectable Drug Product Technology Transfer
Alexion Pharmaceuticals, Inc. is seeking an Associate Director to lead the development and technology transfer of sterile injectable drug products. The role involves overseeing cross-functional teams, ensuring compliance with GMP regulations, and mentoring junior staff while driving continuous improvements in the technology transfer process.
BiotechnologyHealth CareMedicalTherapeutics
Responsibilities
Lead cross-functional teams in the design, execution, and oversight of injectable drug product technology transfers to internal and external GMP manufacturing sites
Develop and implement robust, phase-appropriate technology transfer and process validation strategies, including risk assessments, FMEAs, and control strategies
Oversee development and optimization of drug product unit operations such as freeze/thaw, mixing, sterile filtration, aseptic filling, lyophilization, stoppering, sealing, and visual inspection
Serve as the technical lead during manufacturing campaigns, providing on-site support, troubleshooting, and decision-making in collaboration with Process Development, QA, and Operations
Author and review technical documentation including batch records, validation protocols, change controls, deviations, and regulatory filings (IND, IMPD, BLA, MAA)
Monitor and trend process performance data; lead investigations and implement CAPAs as needed
Collaborate with internal and external stakeholders to ensure alignment on timelines, deliverables, and technical strategy
Lead or contribute to continuous improvement initiatives to enhance the efficiency and effectiveness of technology transfer and manufacturing support processes
Stay current with industry trends, regulatory expectations, and emerging technologies in injectable drug product development
Mentor junior staff and contribute to resource planning, budgeting, and departmental strategy
Travel domestically and internationally (~25%) to support manufacturing site activities
Qualification
Required
Proven leadership in injectable drug product development and technology transfer, including experience with biologics and complex modalities
Deep technical knowledge of sterile manufacturing processes and equipment, including single-use systems
Strong understanding of GMP regulations, process validation, and regulatory submission requirements and supporting regulatory inspections as a technical SME
Experience managing or mentoring technical staff and leading cross-functional project teams in direct or matrix teams through late-phase development and commercial product launches
Proficiency with electronic quality systems (e.g., TrackWise) and data analysis tools
Excellent communication, collaboration, and problem-solving skills
Ability to work in GMP environments and travel as needed for manufacturing support
Prior work with CDMOs and global manufacturing networks
Familiarity with protein formulation, stability, and analytical methods
Preferred
Ph.D. in Chemistry, Biochemistry, Pharmaceutical Sciences, or Engineering with 8+ years of experience; M.S. with 12+ years; or B.S. with 15+ years in biopharmaceutical drug product development and manufacturing
Lean Six Sigma or continuous improvement training
Company
Alexion Pharmaceuticals, Inc.
Alexion, AstraZeneca Rare Disease is focused on pioneering new possibilities for the rare disease community.
H1B Sponsorship
Alexion Pharmaceuticals, Inc. has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (49)
2024 (57)
2023 (51)
2022 (29)
2021 (27)
2020 (17)
Funding
Current Stage
Public CompanyTotal Funding
$5.8M2020-12-12Acquired
1999-02-12Post Ipo Equity· $5.8M
1996-02-29IPO
Leadership Team
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2025-12-20
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