Analytical Development Scientist – Injectables

Chemo; Azuqueca de Henares; Presencial; EUR 45.000 - 70.000; Jornada completa

Descripción de la vacante

INSUD PHARMA, part of the Chemo group, seeks an Analytical Development Scientist to develop, validate and transfer analytical methods for injectable products and materials. You will support formulation development, stability studies, and QC activities, coordinating internal and external work to meet GMP timelines.

Please bring a MSc in Analytical Chemistry or Pharmacy and at least 3 years of hands-on experience in Liquid Chromatography within a GMP environment, plus strong English/Spanish

Formación

• MSc in Analytical Chemistry or Pharmacy required with strong analytical chemistry content.
• At least 3 years in pharmaceutical industry using LC/UPLC/HPLC in GMP environment.
• Experience with method validation and transfer to QC laboratories.
• Fluent English and Spanish written communication.

Responsabilidades

• Develop, validate, and transfer analytical methods for injectable drug products and materials.
• Support formulation development, stability studies, and QC activities with robust analytics.
• Coordinate internal and CRO analytical work in Spain and abroad.
• Ensure successful method transfer to Quality Control labs and write specs, reports, and bulletins.
• Review analytical results and coordinate lab analysts’ activities.
• Prepare documentation for regulatory and clinical activities and manage raw material testing.

Conocimientos

Analytical instrumentation

Chromatography

Mass Spectrometry

GMP/ICH knowledge

English and Spanish written

Educación

MSc in Analytical Chemistry or Pharmacy

Herramientas

HPLC/UPLC

Regulatory documentation tools

Descripción del empleo

INSUD PHARMA, part of the Chemo group, seeks an Analytical Development Scientist to develop, validate and transfer analytical methods for injectable products and materials. You will support formulation development, stability studies, and QC activities, coordinating internal and external work to meet GMP timelines.

Please bring a MSc in Analytical Chemistry or Pharmacy and at least 3 years of hands-on experience in Liquid Chromatography within a GMP environment, plus strong English/Spanish