Bioanalytical Principal Investigator- Scientist I Immunoassay

Alliance Pharma Inc
  • Malvern, PA
    30+ days ago

    Job Description

    • Develop, validate, and troubleshoot bioanalytical methods for sample testing and data reporting, serving as the BPI as required.
    • Present and interpret data both internally and externally, ensuring clarity and scientific rigor.
    • Maintain client satisfaction through timely communication, responsiveness, and on-schedule delivery of high-quality results.
    • Prepare and review laboratory data and controlled documents, including study plans and final reports.
    • Support laboratory operations and provide mentorship to junior staff members.
    • Contribute to the development and refinement of policies, procedures, work instructions, and standard operating procedures (SOPs).
    • Ensure compliance with company standards, including Code of Conduct, Environmental Health and Safety (EHS), and GLP/GCP/GDP regulations.
    • Perform additional duties as assigned to support team and organizational goals.
    • BA/BS or higher with 7-8 years lab experience; all experiences will be evaluated
    • Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11, GDP, GMP and demonstrated experience working in GLP/GCP regulated laboratories.
    • Ability to independently perform complex lab work
    • Ability to work in a regulated environment
    • Ability to work effectively and contribute within a team
    • Ability to work with computer systems
    • Ability to document clearly
    • Knowledge of and experience in a regulatory environment
    • Experience with ligand binding assays (ELISA, MSD, Gyros)
    • Experience with biomarker and/or immunogenicity assays
    • Experience with LIMS
    • Proven ability to lead complex scientific programs and interact directly with clients and regulators.

    We are seeking an experienced Bioanalytical Principal Investigatory (BPI) Scientist I to provide scientific leadership within our bioanalytical contract research organization. This role is ideal for a scientist with deep technical expertise in bioanalysis, a strong understanding of regulated environments, and a proven ability to guide complex programs from method development through clinical and regulatory submission.

    The BPI will serve as a scientific authority, interact directly with clients, and contribute strategically to the growth of our bioanalytical capabilities.

    The successful candidate will:

    • Perform and lead complex lab work, sample analysis, validation, and method development with limited supervision
    • Serve as a subject matter expert in bioanalytical assay development, validation, and sample analysis for biologics, and/or biomarkers.
    • Design and oversee complex bioanalytical strategies supporting preclinical, clinical, and regulatory programs.
    • Provide scientific oversight for troubleshooting methods, data interpretation, and investigative studies.
    • Ensure studies are conducted in compliance with GLP, GCP, and regulatory guidelines (FDA, EMA, ICH).

    Author, review, and approve bioanalytical protocols, validation reports, and study reports.

    Numbers & Facts

    LocationMalvern, PA

    Skills

    • Analysis Skillsunmatched
    • Assay Developmentunmatched
    • Assaysunmatched
    • Biomarkersunmatched
    • Clinical Practices/Protocolsunmatched
    • Clinical Supportunmatched
    • Code of Federal Regulationsunmatched
    • Computer Systemsunmatched
    • Contract Research Organization (CRO)unmatched
    • Corporate Complianceunmatched
    • Customer Relationsunmatched
    • Customer Satisfactionunmatched
    • Document Managementunmatched
    • Drug Developmentunmatched
    • Environmental Healthunmatched
    • FDA Requirementsunmatched
    • GCP (Good Clinical Practices)unmatched
    • GLP (Good Laboratory Practices)unmatched
    • GMP (Good Manufacturing Practices)unmatched
    • ICH Regulationsunmatched
    • Identify Issuesunmatched
    • Immunoassaysunmatched
    • Laboratoryunmatched
    • Laboratory Information Management System (LIMS)unmatched
    • Laboratory Operationsunmatched
    • Leadershipunmatched
    • Ligand Bindingunmatched
    • Maintain Complianceunmatched
    • Mentoringunmatched
    • Operational Supportunmatched
    • Policy Developmentunmatched
    • Quality Assurance Methodologyunmatched
    • Regulationsunmatched
    • Regulatory Complianceunmatched
    • Regulatory Requirementsunmatched
    • Regulatory Submissionsunmatched
    • Safety/Work Safetyunmatched
    • Specimens/Samplesunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Test Dataunmatched
    • Testingunmatched
    • Time Managementunmatched
    • Validation Planunmatched
    • Writing Skillsunmatched

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