Senior Quality Operations Manager

2 weeks ago


Alameda, California, United States Enigma Search Full time
Job Title: Sr. Manager

Enigma Search is seeking a highly experienced Sr. Manager to lead our Quality Operations team. As a critical member of our organization, you will be responsible for providing Quality oversight of our cell and gene therapy manufacturing facility, ensuring successful execution and maintenance of established processes and procedures.

Key Responsibilities:

  • Provide leadership for Quality oversight of cGMP operations, including support for Manufacturing, Laboratory, and Warehouse Operations
  • Execute and improve process and procedures for batch record review
  • Support risk management activities and approve risk management reports
  • Serve as a subject matter expert and support communications with customers on Quality topics and project plans
  • Serve as a subject matter expert for Health Authority inspections and internal audits
  • Establish and execute material and product disposition activities, in compliance with US and EU requirements
  • Support new product introduction activities, including Quality oversight of tech transfer
  • Collaborate with Quality Validation to support oversight of facilities and engineering-related processes for equipment, facilities, and utilities, post qualification
  • Quality oversight activities for deviations, CAPAs, change controls, and laboratory investigations
  • Manage performance and development of direct reports

Requirements:

  • BA or BS in life science degree
  • 8+ years of experience in the pharmaceutical or biotechnology industry in Quality Assurance or Quality Systems or equivalent combination of education and work experience
  • Demonstrated experience in Quality Operations functions within a GMP facility of cell/gene therapy products or biologics in both clinical and/or commercial settings
  • Previous experience in Quality Operations, in start-up or operational settings
  • Ability to effectively prioritize and deliver high-quality results on tight timelines
  • Extensive knowledge of cGMPs
  • Excellent written, verbal communication, and presentation skills
  • Resilient leader and willing to collaborate across cross-functional teams


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