Quality Supervisor, cGMP Raw Materials & Audits

Langham Logistics

Easton (Northampton County)

Vor Ort

USD 80.000 - 110.000

Vollzeit

14 Tage+
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Zusammenfassung

Langham Logistics seeks a Quality Supervisor to lead the Raw Material Warehouse and Sampling Suite, ensuring strict cGMP compliance and rigorous documentation. This on-site leadership role balances hands-on validation with quality systems governance.

You will manage floor staffing, oversee environmental monitoring, instrument-based inspections, CAPA and deviations, and serve as the primary contact for client and regulatory audits.

Qualifikationen

  • Bachelor’s degree in a scientific or technical discipline or equivalent professional experience.
  • Minimum 3 years of hands-on Quality experience in a cGMP-regulated environment (pharma/biotech/medical devices).
  • Previous supervisory or managerial experience is required with ability to coach and manage headcount and schedules.
  • Deep understanding of cGMP, GDP, and GDocs as they apply to raw materials handling and regulatory frameworks.
  • Proficient in MS Office and ability to review complex quality data and implement compliant solutions.

Aufgaben

  • Plan daily floor manpower and allocate tasks based on priorities.
  • Govern the cGMP Sampling Environment with strict cleanroom oversight and contamination control.
  • Execute material quality control by inspecting incoming raw material lots and using analytical tools to verify specs.
  • Drive quality systems including deviations, CAPA, and change controls; cross-train staff for data retention and integrity.
  • Host external and regulatory audits as primary quality contact and ensure audit defensibility.

Kenntnisse

Leadership
Analytical thinking
Problem solving
Collaboration

Ausbildung

Bachelor’s degree in science/technical field

Tools

LIMS
Raman spectroscopy
Calipers
Gauges

Jobbeschreibung

Langham Logistics seeks a Quality Supervisor to lead the Raw Material Warehouse and Sampling Suite, ensuring strict cGMP compliance and rigorous documentation. This on-site leadership role balances hands-on validation with quality systems governance.

You will manage floor staffing, oversee environmental monitoring, instrument-based inspections, CAPA and deviations, and serve as the primary contact for client and regulatory audits.

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