QC Analyst I – cGMP Lab Specialist (Pharma)

Orano

United States

Presencial

USD 65.000 - 85.000

Jornada completa

Hace 8 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Health, Dental, Vision insurance
401(k) with match
Life Insurance
Disability insurance
Paid Time Off
Training and development opportunities

Descripción de la vacante

Orano Med in Brownsburg, IN is seeking a QC Analyst to perform cGMP testing of final products, in-process materials, raw materials, and stability samples. You will help write and optimize methods, validate techniques, and qualify lab equipment.

The role emphasizes accurate data, CofA preparation, environmental monitoring, and collaboration in a dynamic, regulated setting with comprehensive benefits.

Formación

  • Experience in a regulated laboratory environment is required.
  • Proficiency with HPLC, MS, and CE methods is essential.
  • Strong documentation and data integrity proficiency.
  • Excellent written and verbal communication skills.
  • Ability to work independently in a team-based setting.

Responsabilidades

  • Perform testing on final products, in-process materials, raw materials and stability samples.
  • Execute a range of methods including chromatography, spectroscopy and radionuclide assays.
  • Review test records and report quality anomalies per protocols.
  • Contribute to method validation and equipment qualification.
  • Prepare CofA summaries and stability data tables.
  • Maintain laboratory supplies and assist in validations.

Conocimientos

Analytical thinking
Organizational skills
Written communication
Verbal communication
Teamwork

Educación

Chemistry degree

Herramientas

HPLC
Mass Spec
Capillary electrophoresis

Descripción del empleo

Orano Med in Brownsburg, IN is seeking a QC Analyst to perform cGMP testing of final products, in-process materials, raw materials, and stability samples. You will help write and optimize methods, validate techniques, and qualify lab equipment.

The role emphasizes accurate data, CofA preparation, environmental monitoring, and collaboration in a dynamic, regulated setting with comprehensive benefits.

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