QC Manager

Role Overview

• Oversight for Bioanalytical LBA Studies
• Ensure QC activities adhere to GLP regulations (FDA 21 CFR Part 58, OECD GLP) and bioanalytical industry expectations (FDA/EMA BMV guidance).
• Assign QC reviewer to the studies and maintain QC review capacity to ensure timely delivery of QC’ed data/reports/deliverable with high quality.
• Oversee QC review of study data and study integrity.
• Provide guidance and training to QC team to establish/optimize sustainable review process and improve the effectiveness and accuracy of QC review.
• Lead QC review of validation protocols, sample analysis plans, plate layouts, run sheets, and controlled forms.
• Ensure GLP sample analysis is performed according to validated methods, study protocols, and SOPs.
• Confirm integrity of electronic data (ELN/LIMS, plate reader software, instruments outputs).
• Review bioanalytical reports, validation summaries, run acceptance decisions, and performance qualification documentation.
• Collaborate with PI/RS, Bioanalytical Scientists, and QA to address errors, deviations.
• Lead, train, and mentor QC reviewers and specialists supporting the workflows.
• Allocate workloads to meet numerous parallel GLP validation and sample-analysis timelines.
• Maintain a highly organized QC workflow to support fast-turnaround studies and late-stage clinical sample testing.
• Build competency in reviewing complex LBA datasets, including multiplex assays, bridging assays, ADA/NAb workflows, biomarker assays and pharmacokinetics (PK) immunoassays.
• Oversee controlled documents including QC training documentation, controlled forms, templates, QC checklists and relevant QC documents.
• Support and review deviations, investigations and reports/reports templates.
• Ensure reviewed study documents meeting the GLP compliance and follows SOPs.
• Establish QC metrics (review cycle time, error rates, audit observations) and drive continuous process improvements.
• Provide feedback on process gaps, such as data integrity gaps in LIMS or instrument workflows (e.g., SoftMax Pro, MSD Discovery Workbench, SIMOA software).

Requirements

• Bachelor’s or Master’s in Biology, Biochemistry, Immunology, Biotechnology, or related field.
• 5–10+ years of experience in regulated bioanalytical laboratories.
• Strong background in GLP compliance and regulated bioanalysis.
• Minimum 2–5 years of supervisory or leadership experience in QC, QA, or bioanalytical data review roles.
• Strong understanding of GLP and FDA/EMA bioanalytical method validation (BMV) guidance.
• Expertise in immunoassay data review: plate performance, curve fitting models, QC trends, and analytical run acceptance.
• Proficiency with relevant software (SoftMax Pro, E-WorkBook, Watson LIMS, ELN/LIMS systems).

Benefits

• Health insurance
• Paid time off
• Professional development opportunities