Frontage Laboratories·Exton, Pennsylvania
The Associate QC Specialist independently reviews bioanalytical data, laboratory documentation, and study reports to ensure accuracy, completeness, and compliance with GLP and SOPs for Large Molecule studies. This role involves verifying analytical datasets, validating report content, and preparing high-quality data tables for client deliverables.
Title: Associate QC Specialist
Department: Large Molecule
Location: Exton, PA
Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
The Associate QC Specialist supports quality control activities for Large molecule (PK, PD, ADA, Nab etc.) bioanalytical studies conducted in a GLP-regulated contract research organization (CRO) environment. This role is responsible for the independent quality review of bioanalytical data, laboratory documentation, and study reports to ensure accuracy, completeness, and compliance with Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP), and sponsor requirements.
The position plays a key role in ensuring the integrity of data delivered to clients by reviewing analytical datasets, validating report content, and supporting preparation and quality control of data tables used in clinical and regulatory reports.
Roles & Responsibilities
Bioanalytical Data QC Review
Perform independent quality control review of biomarker bioanalytical data including laboratory notebooks, raw instrument data, electronic files, and Laboratory Information Management System (LIMS) records.
Verify accuracy, traceability, completeness, and consistency of analytical data in accordance with SOPs, GLP regulations, and study protocols.
Identify discrepancies or documentation gaps and work with laboratory scientists and study teams to resolve issues prior to final reporting.
Market context
In Pennsylvania, Associate QC Specialist roles are typically tied to steady demand in regulated life science and bioanalytical settings, where employers need candidates who can support quality review and lab workflows. These roles are competitive because they often ask for a relevant bachelor’s degree, some hands-on QC or bioanalytical experience, and familiarity with assays and scientific report review. Before applying, compare the AI-summarized requirements and benefits here with the original posting so you can quickly confirm fit and save research time.
Study Report Review
Review method development, qualification, and validation reports to ensure scientific accuracy and consistency between narrative text, tables, figures, and source data.
Review bioanalytical sample analysis reports for completeness, data integrity, and compliance with internal procedures and client requirements.
Ensure reported results are supported by verified raw data and documentation.
Data Tables and Client Deliverables
Prepare and QC bioanalytical result tables for clinical study reports and biomarker testing reports.
Review and interpret client Data Transfer Specifications (DTS) to ensure correct formatting, variable definitions, and dataset structure.
Generate, QC, and transmit client-ready datasets and data tables according to sponsor specifications and project timelines.
Data Integrity and Compliance
Ensure all QC review activities maintain data integrity and meet regulatory expectations.
Maintain documentation supporting QC review processes for audit and inspection readiness.
Assist in maintaining standardized templates and QC checklists to support efficient report review.
Cross-Functional Collaboration
Collaborate with laboratory scientists, project managers, data management teams, and quality assurance personnel to support timely study reporting and client deliverables.
Communicate QC findings clearly and track issue resolution to ensure high-quality final reports.
Additional Responsibilities
Support continuous improvement initiatives for QC processes and documentation standards.
Assist with preparation for internal audits and regulatory inspections.
Perform other duties as assigned.
Salary and Benefits
Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.
Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.
Candidates need a Bachelor’s degree in a relevant life science discipline and 0–3 years of experience in a bioanalytical lab or QC role within a regulated environment. Required technical skills include familiarity with bioanalytical workflows (like ligand-binding assays), reviewing scientific reports, and proficiency with LIMS and Microsoft Office tools.
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