QC Analytical Associate I
: Job Details :

Job Title: Quality Control Analytical Associate IIf you think you are the right match for the following opportunity, apply after reading the complete description.Location: Mahwah, NJ areaSchedule: 2nd Shift, Sunday-Thursday (2:30 pm to 11 pm)Type: Contract to HireResponsibilities: Support clinical and commercial production through testing and quality control.Perform process checkpoint, stability, and release analytical testing to ensure product quality.Execute company/client test methods for cellular products to ensure safety/efficacy.Maintain, monitor, and troubleshoot laboratory equipment.Document and report test results following cGMP and GTP guidelines.Participate in proficiency testing, equipment validation, and reagent/media preparation.Investigate out-of-spec results and prepare deviation reports.Implement corrective actions and document compliance with SOPs, cGMP, and GDP.Communicate with teams, departments, and clients as needed.Requirements: Education: BA/BS in Science or related field.Experience: 0-2 years in Quality Control or biopharmaceutical industry; cGMP experience preferred.Skills: Familiarity with lab equipment (cell count, flow cytometry, CBC).Proficient with Microsoft Office and Visio.Strong written and oral communication skills.Prior experience with cell therapeutic work preferred.Compliance & Regulatory: Ensure adherence to FDA and global quality regulations.Attend required Quality & Compliance training.Benefits: Health, dental, and vision insurance options.401(k) participation and life insurance.Keywords: GTP , Good Tissue Practices , Good Documentation Practices , GDP , cell therapy , cell therapeutic , cellular products , cell count , flow cytometry , CBC , basic laboratory equipment