What are the responsibilities and job description for the Quality Control Associate position at ClinLab Staffing?
QC Analytical Associate II – Allendale, NJ
Our vision is creating future cell therapy miracles together. We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies, and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company.
The Quality Control Analytical Associate II serves as a supporting role to clinical and commercial production. The QC Analytical Associate II will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility.
Essential Functions and Responsibilities
Performs the accurate execution of all company and / or client test methods and procedures of cellular products to ensure the safety and / or efficacy of different cell populations
Performs maintenance, monitoring, and troubleshooting of pertinent equipment
Performs and assists in the training of other Quality Control technicians
Maintains training records and coordinates records retention with Document Control and Training groups
Tests, documents, and reports results for products or materials following company and / or client procedures following CGMP and / or GTP guidelines
Performs state proficiency testing and / or client proficiency testing under direct supervision as applicable
Participates in managing QC materials and supplies
Performs and assists in equipment and method qualification / validation activities as needed
Performs reagent and media preparation
Provides input based on level of knowledge and experience with troubleshooting malfunctioning equipment
Investigates out-of-specification, out-of-trend, aberrant, and / or non-conforming test results
Initiates, investigates, and prepares deviation reports with input from assigned supervisor
Brainstorms and implements corrective and preventive actions, as and when applicable
Documents training and execution of shipping test samples to contract laboratories for testing
Completes all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP)
Communicates effectively with other co-workers, departments, management and clients
Eventually serves as a lead and / or co-lead for client projects
Additional tasks as assigned
Qualifications and Competencies :
BA / BS in a science or relevant field required
Experience in GMP, cell count, flow cytometry, documentations, flexibility, CBC, ELISA, qPCR
Prior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a cGMP / GTP environment preferred
Prior industrial experience in cell count methodologies preferred
Prior academic and / or industrial cell therapeutics experience preferred
Minimum 2-4 years of experience in QC lab setting or withing biopharma industry
