Job Details
Posted 1 May, 2026
Job Id: 627669
Quality Control Review Resource I (GPV)
Job Description
Pay 40-50/h depending on experience
Conduct quality control (QC) review, including verification of data against approved supporting documentation/sources for aggregate reports. Performs data integrity review of CMC data and reports intended for regulatory filings. Ensures integrity, accuracy, and consistency of data and documents. Record QC metrics per defined categories.
Requirements: BA/BS or equivalent with typically 3+ years relevant experience in a biotechnological and/or pharmaceutical Quality Assurance setting. Experience in a pharmaceutical development environment with knowledge and review experience on development study protocols and reports for investigational stage products. Excellent oral and written communication skills. Ability to perform and verify mathematical determinations utilizing both calculator and computer programs, such as MS Excel. Ability to work effectively in a matrix setting to resolve issues and achieve common goals
Preferred: Previous experience with cell therapy development or cell-based assays (technical or quality review). Experience working under GxPs and/or knowledge of GMP, ICH, USP and global compendial regulations and guidance.
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
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