QA/QC Director: Lead Quality & Compliance in Biopharma

ProcessHQ, Inc.

California

On-site

USD 180,000 - 240,000

Full time

14 days+

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Job summary

ProcessHQ, Inc. seeks a QA/QC Director to oversee all quality assurance and quality control activities, ensuring cGMP compliance, regulatory alignment, and adherence to company standards. You will drive QMS, audits, CAPAs, investigations, and training.

The role requires a strong scientific background, 5+ years in regulated industries with 3–5 years in management, and a Bachelor's degree in a related field. Leadership is essential to mentor staff and meet KPI targets.

Qualifications

  • 5+ years of experience in pharmaceutical, biotechnology, or related regulated industries.
  • Minimum of 3-5 years of management experience in QA/QC, or Quality Operations.
  • Experience with investigations, CAPA management, and root cause analysis.
  • Familiarity with validation, qualification, and stability programs.
  • Strong understanding of data integrity requirements and regulatory expectations.

Responsibilities

  • Develop, implement, and maintain Quality Management Systems in compliance with ISO 9001-2015.
  • Manage deviations, CAPAs, change controls, risk assessments, and product quality complaints.
  • Ensure compliance with cGMP, GDP, and data integrity requirements.
  • Lead internal audits and support customer audits.
  • Oversee training programs related to quality systems and GMP compliance.
  • Lead, mentor, and develop QC/QA personnel.
  • Establish departmental goals, KPIs, and performance objectives.

Skills

Quality management systems
GMP compliance
Leadership & mentoring
Audits & regulatory inspections
CAPA management
Root cause analysis
Validation/qualification/stability
Data integrity
Regulatory expectations

Education

Bachelor's degree in a scientific discipline

Job description

ProcessHQ, Inc. seeks a QA/QC Director to oversee all quality assurance and quality control activities, ensuring cGMP compliance, regulatory alignment, and adherence to company standards. You will drive QMS, audits, CAPAs, investigations, and training.

The role requires a strong scientific background, 5+ years in regulated industries with 3–5 years in management, and a Bachelor's degree in a related field. Leadership is essential to mentor staff and meet KPI targets.

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