Quality Assurance Line Inspector

Lakewood - 1200 Paco Way, Lakewood, NJ 08701, USA

Pay or shift range: $25.33 USD to $27.54 USD. The estimated range is the budgeted amount for this position. Final offers are based on various factors, including skill set, experience, location, qualifications and other job-related reasons.

• Perform Quality Assurance tasks including production line clearances, sampling, inspections, and quality attributes testing designed.
• Guiding the production team on quality control measures to improve product excellence.
• Sets up and performs destructive and nondestructive tests on materials, parts, or products to measure performance, or material characteristics.
• Help develop, modify, apply, and maintain quality standards and evaluation methods for products and processes.
• Qualify on visualinspection of in-process materials.
• Provide oversight of activities on manufacturing floor; working with operations personnel to achieve and maintain compliance.
• Monitor manufacturing areas during operations to ensure that batch documentation requirements and SOPs are being followed.
• Review all documentation related to the manufacturing processes for accuracy and compliance, both online and upon completion of the activity.
• Ability to gown to Grade B standards and perform quality inspection inside cleanroom areas.
• Assist with investigations related to non-conformances within manufacturing or during storage.
• Collect representative samples for testing and retention, and ensure all relevant paperwork is complete. Submit samples/resamples to laboratory in a timely fashion to meet production needs.
• Sample in-process items and finished products. Perform required inspections and testing of in-process items and finished products.
• Apply disposition stickers to components, in-process materials and finished products.
• Responsible for control of label and inserts during manufacturing activities as well as issuing reports and verifying materials against associated staging sheet.
• Responsible for reconciling unused labels and inserts and their destruction.
• Process and distribute samples to other teams (i.e.: Quality Control Laboratory) for evaluation and testing.
• Ensures all documented data, whether on paper or in an electronic system, follow the principles of ALCOA+:
  Attributable, Legible, Contemporaneous, Original, and Accurate.
• Maintain a clean and safe environment in compliance with State and Federal regulatory guidelines.
• Ability to work with computer-based systems and equipment.
• Perform other duties and responsibilities as assigned

Associates Degree is required. Bachelor’s Degree is preferred. Science or engineering degrees is preferred. Previous pharmaceutical experience is a plus.

Equal Opportunity Employer
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