QC Specialist

QC Specialist

Contract Type:

Full Time

Location:

Garden Grove

Industry:

Pharmaceuticals

Contact Name:

Kori Eckert

Contact Phone:

Date Published:

26-Jun-2025

Responsibilities

  • Review and release product documents to ensure that products meet requirements prior to manufacturing
  • Procure samples for laboratory testing
  • Provide and test product status to appropriate personnel and departments
  • Investigate and resolve labor variances
  • Conduct investigation of customer complaint evaluation testing and provide investigation summaries
  • Respond to customer complaints by communicating effectively with customers and conducting through investigations and producing final reports
  • Prepare and execute product stability testing schedule and oversee testing functions
  • Recommend disposition for discrepant materials and troubleshoot manufacturing problems as appropriate
  • Determine and assign controls as appropriate
  • Evaluate and revise work instructions, standard operating procedures, MPS and Product Performance Specifications for management review and approval
  • Participates in new product development projects
  • Develop evaluation procedure, test procedures and training for new products to end users and employees
  • Monitor and maintain calibration and proper function of laboratory instruments and equipment
  • Audit and review calibration records
  • Evaluate and develop highly technical, specialized laboratory testing and determine material disposition for raw material, in-process components, and finished goods
  • Interact with all co-workers and management in a positive, supportive and cooperative way
  • Create and maintain quality in an ever-changing and developing environment

Qualifications

  • BS degree in biological science or relevant discipline
  • 1+ year of quality control experience in the medical device industry
  • Previous experience working with computer systems and software pertaining to product manufacturing and inventory management (ERP systems) preferred
  • Working and applied knowledge of GMP, ISO 13485 and standard laboratory practices
  • Working knowledge of common laboratory equipment
  • Planning and scheduling ability, to analyze and investigate product failures
  • Working knowledge of the manufacturing process
  • Ability to follow instructions carefully with attention to detail

...

Apply Now
Apply Now

Share this job

Interested in this job?
Save Job
Create As Alert

Similar Jobs

SCHEMA MARKUP ( This text will only show on the editor. )