We are seeking a Senior Process Development Scientist to support sterile drug product manufacturing operations within the pharmaceutical or biotechnology industry. The ideal candidate will have strong expertise in aseptic processing, process characterization, process validation, technology transfer, data analysis, and commercial process support. This role requires the ability to work cross-functionally while providing scientific and technical leadership to support manufacturing readiness and continuous process improvement.

Requirements

A degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Bioprocess Engineering, Pharmaceutical Sciences, Biotechnology, Biology, Microbiology, or a related scientific discipline is highly preferred. Doctorate (PhD, PharmD, or MD) with relevant postdoctoral experience where applicable; or Master's degree with 3+ years of relevant scientific experience; or Bachelor's degree with 5+ years of relevant scientific experience.
Experience with statistical software (JMP or Minitab) and Sample Management System such as LIMS and HLEE.
Experience supporting sterile drug product manufacturing within the pharmaceutical or biotechnology industry.
Hands-on experience with aseptic filling operations, process characterization, process validation (PPQ), technology transfer, and commercial process support.
Experience authoring and executing validation protocols, characterization studies, technical reports, investigations, and change controls.
Strong knowledge of GMP requirements, aseptic processing principles, contamination control strategy, and pharmaceutical quality systems.
Experience performing statistical analysis using JMP or Minitab and applying data-driven approaches to process optimization.
Ability to analyze manufacturing data, identify process trends, and recommend scientifically sound solutions.
Experience working in cross-functional teams with Manufacturing, Quality, Engineering, Regulatory, and Technical Services.
Strong technical writing, communication, presentation, and project management skills.
Ability to independently manage multiple projects in a fast-paced manufacturing environment while supporting commercial readiness and continuous process improvement.
Experience with single-use technologies, filling equipment, and sterile manufacturing operations is highly desirable
Fully Bilingual (English and Spanish)

Compétences requises

Aseptic filling operations (aseptic processing)Process characterizationProcess validation (PPQ)Technology transfer to manufacturingCommercial process support for sterile drug productsStatistical analysis using JMP or MinitabSample management systems (LIMS, HLEE)Good Manufacturing Practice (GMP) and pharmaceutical quality systemsContamination control strategy developmentManufacturing data analysis and process trend identificationTechnical writing and authoring validation/characterization reports and protocolsCross-functional collaboration with Manufacturing, Quality, Engineering, Regulatory, Technical ServicesProject management and ability to manage multiple projectsExperience with single-use technologies and filling equipmentBilingual communication (English and Spanish)

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