Quality Control Specialist - Precision & Impact (Onsite TX)

MeDisc

Irving (TX)

Presencial

USD 45 000 - 65 000

Tempo integral

14 dias+

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

PTO & holidays
Health savings account
Career growth
401k plan
Employee Referral Program
Company events
Safety shoes provided

Resumo da oferta

Medisca in Irving, Texas is hiring a QC Specialist to support the Quality Control department on-site. You will participate in receiving, quarantining, releasing products, calibration, maintenance, and document control to ensure quality and compliance.

The role requires at least an associate or bachelor's in a science field or pharma experience, plus 1 year in QC, attention to detail, and strong MS Office skills. Safety and teamwork are emphasized.

Qualificações

  • Associates or Bachelor's in science or pharma-related experience.
  • Minimum 1 year in Quality Control environment.
  • Detail-oriented with good judgment.

Responsabilidades

  • Receive, inspect, quarantine and release chemical and device bulk products.
  • Maintain quarantine areas.
  • Maintain calibration and maintenance schedules.
  • Schedule calibration and maintenance services.
  • Monitor environmental conditions at the location.
  • Perform investigations (Deviations, NC/MR, CAPAs, SCARs).
  • Initiate Change Controls.
  • Quality review of documents.
  • File and organize documentation; support QC inspectors as needed.

Conhecimentos

QC experience (1 year)
Attention to detail
Decision making
MS Office (Word/Outlook/Excel)
Physical ability

Formação académica

Associates/Bachelor’s degree in Science or related field

Ferramentas

Syspro
MasterControl

Descrição da oferta de emprego

Medisca in Irving, Texas is hiring a QC Specialist to support the Quality Control department on-site. You will participate in receiving, quarantining, releasing products, calibration, maintenance, and document control to ensure quality and compliance.

The role requires at least an associate or bachelor's in a science field or pharma experience, plus 1 year in QC, attention to detail, and strong MS Office skills. Safety and teamwork are emphasized.

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