Onsite
Full Time IT Management & IT Project Management
Responsibilities:
Define and execute the IT solutions roadmap for CMC digital transformation.
Oversee implementation and lifecycle management of digital CMC solutions to speed new pipeline products from Development Candidate through IND/NDA filings to commercial launch.
Deliver digital and AI/ML capabilities for faster regulatory authoring and reduced error rates via digital tech transfer of Drug Substance/Drug Product/analytical methods and data.
Enable creation, transformation, and storage of recipe master/reference data, transactional lab run data, DOE/batch execution data, and derived statistical/trending outputs.
Standardize/structure process recipe data (CPPs/CCAs/In-Process Controls/operating ranges) with recipe version management.
Develop CMC statistics assets and trending tools; enable CMC program management digitization and reporting.
Create data products, templates, procedures, and seamless integrations (API/EDI) for process data exchange.
Establish process data governance/stewardship and publish data products to support analytics/AI/ML.
Own end-to-end lifecycle of CMC applications (strategy/design through deployment, sustainment, upgrades, continuous improvement, retirement); define business cases and manage TCO.
Ensure GxP/data integrity/global regulatory compliance and audit readiness.
Drive operational excellence for CMC systems (e.g., Empower, SoftMax Pro, Emerson Process Knowledge Management, QbDVision).
Lead and mentor cross-functional delivery; partner with stakeholders, IT, vendors, and procurement.
Qualifications:
Required:
Bachelor’s degree in Science/Engineering/IT or related field.
10+ years in CMC, Process Engineering, or IT client-facing roles in biopharma/life sciences.
Knowledge of regulatory filing, recipe unit operations/data structures; statistical software/trending tools (e.g., JMP, Minitab, R/Python, SIMCA, SEEQ).
Strong stakeholder management/change leadership.
Data and systems integration experience with IT suppliers/integrators.
Regulated environment experience (GxP, computer systems validation, FDA 21 CFR).
SDLC knowledge (requirements through decommissioning).
Proven cross-functional team leadership; strategic + pragmatic delivery.
Up to ~10% travel.
Preferred:
Master’s/MBA/PhD.
Working knowledge of EDI/APIs/data transfers and system integration.