Quality Control Analytical Associate II

Job Description

Job Description

Quality Control Analytical Associate II Allendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device, IT & Human Resources disciplines in New Jersey. The Quality Control Analytical Associate II serves as a support 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. Under the direction of the Manager, QC Analytical Associate II, responsibilities include :

• 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

REQUIREMENTS

Other Information

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice. QC Analytical Associate I is available as well.