Biopharma Quality Assurance Specialist

The Fountain Group
El Segundo, CA
$50-$55 an hour
Full-time

W2 Contract Assignment

Pay Range : $50 - $55 / Hour

Onsite in El Segundo, CA

Overview :

  • Seeking a Senior Specialist of Quality Operations responsible for Product Disposition.
  • This position will participate in Quality activities to ensure compliance with applicable quality objectives and regulatory requirements.

Responsibilities

  • Perform Product Disposition and Lot Closure. Includes commercial and clinical products.
  • Review batch-related documentation and ensure resolution of issues to release product
  • Review batch-related shipment documentation to ensure product shipment remained in control
  • Provide QA oversight and review of deviations tied to lots. Ensure deviations are properly initiated, investigated and resolved in accordance with established disposition timelines.
  • Provide QA oversight and (limited) approval of CAPAs. Ensures that associated CAPAs are initiated and resolved.
  • Provide QA oversight and approval of change records. Ensures that change records are initiated and resolved.
  • Support and participate in investigations, including batch record review.
  • Ensure process control measures are in place and followed in product manufacturing
  • Maintain metrics related to product disposition in support of the Management Review
  • Generate and update procedures, forms and other documents
  • As assigned, manage and provide QA oversight for other processes, including training, warehouse / inventory, redose, new product introductions, etc.
  • Generate and report data for management
  • Maintain production (finite), disposition, and team schedules
  • Represent Disposition or QA Ops at plant and multi-site scheduling meetings
  • Provide QA representation on projects and at team meetings
  • Provide QA representation at multi-site disposition meetings
  • Support and participate in inspections and audits

Basic Qualifications

  • Master’s Degree and 5+ years of experience in GMP environment OR
  • Bachelor’s Degree and 7+ years of experience in GMP environment OR
  • High School Degree and 11+ years of experience in GMP environment

Preferred Qualifications

  • Bachelor’s degree in the biological sciences or related field and minimum of 7 years progressive experience in a pharmaceutical, biotech, or biologics operation, or equivalent education / work experience.
  • Working knowledge and ability to apply GMPs in conformance to U.S. and EU standards
  • 17 days ago
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