Associate Research Scientist - Large Molecule Bioanalysis

Eurofins

India

Presencial

INR 600.000 - 900.000

Jornada completa

Hace 4 días
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Descripción de la vacante

Eurofins in India is seeking an Associate Research Scientist to support development and validation of bioanalytical methods for large molecules in a regulated lab setting. You will work under the Study Director to ensure robust and compliant analyses across ELISA and MSD platforms.

The role emphasizes GLP compliance, meticulous documentation, and collaboration with sponsors, regulators, and auditors to maintain high-quality data for regulatory submissions.

Formación

  • Experience in large molecule bioanalysis (ELISA/MSD)
  • Strong attention to detail and data integrity
  • Familiarity with GLP guidelines and SOPs

Responsabilidades

  • Develop, optimize and validate bioanalytical methods for large molecules under Study Director supervision
  • Ensure GLP compliance and adherence to SOPs and approved protocols
  • Perform immunogenicity assessments with precision and rigor
  • Maintain comprehensive study documentation and data integrity
  • Collaborate with internal teams, sponsors, regulators and auditors to ensure quality
  • Record and manage data using LIMS and contribute to study reports
  • Support regulatory submissions as required

Descripción del empleo

Associate Research Scientist - Large Molecule Bioanalysis
  • Full-time

Position Overview:

The Associate Research Scientist will support the development and validation of bioanalytical and immunogenicity methods within a regulated laboratory environment. This role requires meticulous attention to detail, strong technical expertise in large molecule bioanalysis, and the ability to work collaboratively with cross-functional teams.

Key Responsibilities:

  • Develop, optimize, and validate bioanalytical methods for large molecule analysis using ELISA and MSD platforms under the supervision of the Study Director
  • Execute all laboratory activities in strict adherence to Good Laboratory Practice (GLP) guidelines, standard operating procedures (SOPs), and approved protocols
  • Perform immunogenicity assessments and immunological testing with precision and scientific rigor
  • Maintain comprehensive documentation and data integrity throughout all bioanalytical studies
  • Collaborate effectively with internal teams, sponsors, regulatory agencies, and external auditors to ensure compliance and quality standards
  • Utilize laboratory information management systems (LIMS) to record, track, and manage study data and results
  • Contribute to the preparation of study reports and regulatory submissions as required
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