Quality Specialist
Aequor - Summit, NJ
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Position: Quality Records Specialist 59670-1Location: Summit NJ 07901Duration: 12+ months (possibility of extension for the right candidate depending on performance)Pay rate: $30/ hour on W2100% onsite requiredWork schedule: Mon- Fri(normal business hours)PURPOSE AND SCOPE OF POSITION:The Global Supplier Quality, External QC -Vector will process external deviation and change records from our Contract Test Laboratories (CTL).Other duties may include; Coordinate testing of samples for lot release, PPQ, PSQ, and compiling vendor documentation to generate a CoA/CoT.This role will partner cross-functionally with Global Product Quality, External Manufacturing Supply Chain, and Global Supplier Quality to release vectors in a timely manner for commercial, clinical, and early development programs.REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities:• Experience with deviation and change control management, preferably with Infinity systems• Strong organizational skills, including the ability to follow assignments through to completion• Ability to work in a fast-paced environment, meet deadlines and prioritize work from multiple projects• Excellent verbal and written communication skills, and ability to work within inter-disciplinary and cross-functional teams• Detail-oriented with demonstrated application in problem-solving• With moderate oversight from the manager, think strategically and understand the global impact of decisionsDESIRED COMPETENCIES: Knowledge, Skills, and Abilities:• Advanced project management skills such as process excellence/Six Sigma methods and approaches including process mapping, root cause analysis, and problem definition• Experience within the Cellular Therapeutics and/or gene-based products. Experience with biologics will be considered.Experience with Clinical and/or Commercial product manufacture, supply, and post-approval change management• Knowledge of applicable FDA/EMA regulations in the biotechnology industryExperience managing external suppliers and other supply chain issues• Experience with Quality Systems (change control, deviation, and investigation)Education and Experience: • Preferred Bachelors in a relevant scientific discipline, or 3 years experience in biotherapeutics/biomanufacturing QC/QADUTIES AND RESPONSIBILITIES:• Initiation, facilitation, and tracking of quality records• Provide regular communication and metrics for the status of quality records• Effectively communicate issues, risks, and proposed solutions within the organization• Provide communication, support, and guidance to CTLs within the QA vector and upstream material team• Other duties may include:• Create and revise SOP• Create and revise Certificates of Analysis (CoA) and Certificates of Testing (CoT)• Enter data and retrieve information from SharePoint and Smartsheet testing trackersWORKING CONDITIONS (US Only):• May be required to work in an office environment.• Sitting, standing, and computer work is required.• Ability to participate in conference calls
Created: 2024-10-15