C
Not Specified Permanent

Camarillo, California · USA job

Site Quality Head

Curia

Camarillo, California

Job description

Overview

In this role you lead Curia's on-site Quality organizations (QA, QC) at the Camarillo facility to meet global regulatory and cGMP expectations. You partner with manufacturing operations to ensure GMP compliance and oversee cross-functional quality decisions. You guide implementation of Curia's standards and quality systems to sustain high-quality product care. This position offers impact across QA, QC, microbiology and chemistry labs, shaping site quality and regulatory readiness. You'll drive quality improvement and talent development in a fast-paced, mission-driven environment.

Compensation / Benefits
  • Generous benefit options (eligible first day)
  • Paid training, vacation and holidays
  • Career advancement opportunities
  • Education reimbursement
  • 401K with matching
  • Learning platform
Responsibilities
  • Provide technical oversight and decision support to the VP of Quality Operations
  • Ensure GMP compliance across manufacturing activities from material dispensing to product dispatch
  • Advise on cross-contamination control and global regulatory standards
  • Support new products, process changes, and regulatory affairs alignment
  • Lead quality and compliance process improvements using current regulations and best practices
  • Drive continuous quality and cost improvement initiatives at the site
  • Ensure implementation and maintenance of Curia global Quality Systems
  • Develop and manage Manufacturing QA, Quality Control (chemistry and microbiology) and Quality Systems & Compliance functions
  • Oversee environmental monitoring and stability testing timelines
  • Recruit, develop and retain top talent within the Quality Organization
  • Provide data to management to manage regulatory risk and site productivity
  • Develop and manage the site Quality budget
Key requirements
  • BS or BA in a scientific field, microbiology preferred
  • Minimum 15 years of progressively responsible Quality Operations experience in pharmaceutical/sterile biologics/medical devices sectors
  • Proven leadership and people management skills
  • Effective communication and collaboration abilities
  • communication
  • collaboration
  • leadership
  • GMP compliance
  • quality systems implementation
  • environmental monitoring

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