Quality Assurance Quality Control (QA-QC) Inspector II_JP34488

Now Hiring: QA/QC Inspector II Are you passionate about quality, compliance, and laboratory operations in a GMP environment? We are seeking a Quality Assurance / Quality Control (QA/QC) Inspector II to join a leading biopharmaceutical organization in Worcester, MA. This is an excellent opportunity to support laboratory data review, quality compliance, and regulatory documentation while contributing to the development and manufacturing of innovative biologic therapies. Position Overview As a QA/QC Inspector II (Associate Data Reviewer), you will support the laboratory data review team within a fast‑paced GMP environment. This role is responsible for reviewing laboratory data, ensuring compliance with GMP standards, supporting data integrity initiatives, and maintaining quality documentation across multiple laboratory functions including raw materials, environmental monitoring, in‑process testing, stability, validation, and final product testing. Key Responsibilities Review laboratory test data for accuracy, completeness, and compliance with GMP requirements. Perform both On-the-Floor and Off-the-Floor reviews for routine, low-complexity laboratory testing. Archive laboratory data using the RIMS system. Support laboratory documentation by scanning, filing, organizing, and maintaining records. Assist with logbook management and administrative support for the laboratory review team. Perform data mining activities and support laboratory investigations when needed. Maintain compliance with GMP documentation practices, laboratory procedures, and quality systems. Promote a safe laboratory environment while adhering to company safety policies and procedures. Manage workload effectively to ensure timely completion of assigned tasks. Assist with training new employees through demonstration of laboratory processes and procedures. Required Qualifications Bachelor's Degree in a scientific discipline OR High School Diploma with 5+ years of experience in Quality Assurance, Quality Control, manufacturing, or laboratory operations within the pharmaceutical or biologics industry. Strong organizational and time management skills. Excellent attention to detail and documentation accuracy. Ability to prioritize multiple assignments in a fast‑paced GMP environment. Preferred Skills & Experience Experience using RIMS Experience with Empower Chromatography Data System Familiarity with A280 instrumentation or analytical systems Knowledge of GMP, laboratory documentation, and data integrity requirements Experience supporting pharmaceutical, biologics, or biotechnology manufacturing laboratories Ideal Candidate We're looking for a detail‑oriented quality professional who enjoys working in a collaborative laboratory environment and takes pride in maintaining the highest standards of data integrity and regulatory compliance. The ideal candidate is organized, dependable, and committed to delivering high‑quality work while supporting critical laboratory operations. Why Join This Opportunity? Join a world‑class biopharmaceutical organization Gain experience supporting biologics manufacturing and quality operations Work alongside experienced Quality and Laboratory professionals Excellent opportunity to expand your GMP and Quality Systems experience Competitive contract assignment with potential for future opportunities Interested? Apply today or send your resume for immediate consideration! Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status or disability status. #J-18808-Ljbffr K3-Innovations, Inc.