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QO Investigations Coordinator

Job in Houston, Harris County, Texas, 77246, USA
Listing for: Empower Pharmacy
Full Time position
Listed on 2026-09-01
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
Salary/Wage Range or Industry Benchmark: 65000 - 90000 USD Yearly USD 65000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: QO Investigations Coordinator 503B

Empower Pharmacy is a visionary healthcare company dedicated to making quality, affordable medication accessible to millions of patients nationwide. As the nation’s most advanced 503A compounding pharmacy and FDA-registered 503B outsourcing facility, we’re redefining what’s possible in personalized medicine and pharmaceutical manufacturing. We’re proud to be recognized as one of Houston’s fastest-growing private companies and ranked #116 in Healthcare & Medical on the Inc.

5000 List for 2025.

Our strength is built on four core values:
People, Quality, Service, and Innovation. Guided by these principles, we’ve created a uniquely integrated healthcare platform powered by advanced technology, operational excellence, and a relentless commitment to patient care. From manufacturing and quality control to distribution and customer experience, our teams work together to raise industry standards, expand access to critical medications, and improve outcomes for patients and providers across the country.

At Empower, joining our team means more than starting a new role. It means becoming part of a mission-driven organization that’s transforming healthcare  invest deeply in our people, encourage bold thinking, and create opportunities for growth, leadership, and innovation at every level. Your ideas matter here, your development is supported, and the work you do has a direct impact on the lives of millions.

If you thrive in a fast-moving, purpose-driven environment where innovation, collaboration, and ambition come together, Empower Pharmacy is the place for you. Let’s transform healthcare together.

Position Overview:

The QO Investigations Coordinator supports product integrity and compliant quality operations by coordinating investigation activities, maintaining accurate records, and advancing timely resolution of quality events. Working within Empower’s hyper-growth, highly regulated 503A and 503B environment, this role supports investigations involving deviations, non-conformances, and laboratory or production events while aligning documentation with USP standards, cGMP requirements, and established procedures.

The coordinator gathers and analyzes data, assists with root cause analysis, tracks corrective and preventive actions, and prepares metrics that highlight recurring issues and improvement opportunities. Success requires disciplined execution, sound judgment, strong organization, clear communication, and learning agility.

The role contributes directly to investigation quality, documentation accuracy, CAPA follow-through, operational visibility, continuous improvement, and strong execution consistency while helping protect product quality, patient safety, and regulatory readiness across daily quality operations.

Responsibilities:
  • Data Collection: Collect and organize investigation data for deviations, non-conformances, and laboratory or production events to support accurate, evidence-based assessments.
  • Initial Assessment: Conduct initial event assessments using approved templates and guidance, documenting relevant facts, observations, and potential contributing factors clearly.
  • Investigation Writing: Draft investigation documentation that accurately summarizes evidence, analysis, conclusions, and follow-up requirements in accordance with established procedures.

CAPA and Documentation

  • CAPA Tracking: Track corrective and preventive action commitments, due dates, and follow-up activities to support timely, complete implementation across responsible functions.
  • Record Maintenance: Maintain complete investigation records and supporting documentation, ensuring information remains organized, traceable, current, and aligned with procedural requirements.
  • Compliance Support: Apply cGMP and applicable USP , USP , and USP requirements when documenting investigations and coordinating quality follow-up activities.

Collaboration and Improvement

  • Team Coordination: Collaborate with Quality leadership and cross-functional partners to gather information, resolve documentation gaps, and advance investigations toward timely closure.
  • Trend Reporting: Compile investigation metrics and trending reports that identify recurring issues,…
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