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Quality Engineer
Ref No.: 18-42446
Location: Ridgefield, New Jersey
Position Type:Direct Placement
Pay Rate : $ 80,000.00 - 100,000.00 /Year
Skill Type
Skill Type:Engineering
The Quality Engineer provides compliance support to the manufacturing plant

Under the direct supervision of the Manager, Quality[m1]


To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Primary responsibilities are:
  • Responsible for documentation of non-conformances, customer complaints and CAPA reports into QCBD and lead investigations to close the documents to completion. . Forward documents to customer as necessary and responds to customer concerns with regards to quality.
  • Develop and maintain documents which support the Quality Management System (QMS)
  • Responsible for project management/oversight of plant improvements.Interface with customers and review data during first production fill trials.
  • Perform cGMP audits throughout the facility.
  • Participate in the training of Line Leaders/Techs and Assembly personnel for new product fills.
  • Support the internal quality auditing system.Record and analyze data from first production fills and trial runs and communicate formal report and findings back to the production team and the customer.
  • Play a key role in all customer and regulatory audits
  • Develop and applies technical quality assurance protocols/methods for both product and process improvement.
  • Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations
  • Performs analysis and identifies trends in products and processes and recommends corrective actions when necessary
  • Support manufacturing operations from a quality perspective and participates in strategic development activities when requested
  • Track quality assurance metricsAct as Quality Manager backup
  • Perform other duties as needed or assigned
The requirements listed below are representative of the knowledge, skill and/or ability required for his position.
  • Education: Bachelor's Degree in an applied science or engineering field
  • Certifications: None
  • Experience:
  • 3 years prior experience in Quality Assurance for personal care, OTC, Drug or device products
  • Knowledge of ISO 9001 and process improvement tools / techniques and experience
  • Familiar with Validation techniques
  • Must be able to combine and analyze quality data
[m1]Are we leaving this as is. In Roanoke he's reporting to Validation Manager for now.
Nesco Resource is an equal employment opportunity employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or veteran status, or any other legally protected characteristics with respect to employment opportunities.