BRL (Research Associate - R&D) - Analytical

USV

Maharashtra

Sur place

INR 800 000 - 1 200 000

Plein temps

14 jours+
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Résumé du poste

USV Private Limited in Maharashtra is seeking a Research Associate for BRL - Analytical Laboratory to drive analytical deliverables for Biologics projects. You will perform method development, qualification, tech transfer, and biosimilarity assessments across markets, with emphasis on HPLC/UPLC, chromatographic methods, and electrophoresis.

You will plan and execute experiments, maintain data integrity, and prepare technical reports while collaborating with cross-functional teams to meet project

Qualifications

  • 2-5 years of experience in an analytical development laboratory setting.
  • Hands-on experience with HPLC/UPLC and chromatographic modes required.
  • Experience with biotherapeutic proteins and analytical deliverables preferred.

Responsabilités

  • Plan and execute experiments with emphasis on HPLC/UPLC analysis.
  • Apply chromatography, electrophoresis, and spectrophotometry techniques.
  • Maintain data integrity and prepare technical reports.

Connaissances

HPLC/UPLC
Chromatography methods
Electrophoresis
Spectrophotometry
Data integrity
Biologics knowledge

Formation

MSc Biotechnology
MTech Biotechnology
BSc Biotechnology
BTech Biotechnology

Outils

HPLC systems
UPLC systems
CIEF/CZE/CE-SDS
DSC/CD/FTIR

Description du poste

BRL (Research Associate - R&D) - Analytic Laboratory

USV/RA--A/1806781

  • Biotechnology Research Laboratory
  • Maharashtra

Posted On 21 Sep 2026

End Date 30 Nov 2026

Required Experience 2 - 5 years

Basic Section

BAND Junior Management

Designation Executive

Employment Type Employee

Employee Category 1006

Organisational

Company Code USV Private Limited

GRP USV Private Limited

SBU Biologics

Function Biotechnology Research Laboratory

Department BRL - Analytical Laboratory

Country India

State Maharashtra

Skills

Post Graduate

M.Sc. MTech

Job Description

Role Objective: Will work in the Analytical Development Lab of BRL, taking responsibility for the analytical deliverables of Biologics Projects for all markets. Deliverables involve, but are not limited to, Method Development, Qualification, Technology transfer, Biosimilarity assessment, Forced degradation, and Characterization activities.

KEY RESPONSIBILITIES

  • Responsible for the independent planning and execution of experiments, with a major focus on HPLC, UPLC, and CE-based analysis.
  • Apply analytical techniques including, but not limited to, Chromatography, Electrophoresis, Spectrophotometry, and Colorimetric assays for Biotherapeutics.
  • Perform assigned analytical activities by following established systems and procedures.
  • Maintain target dates for all assigned analytical activities.
  • Maintain strict data integrity during all analysis processes.
  • Prepare and review technical reports and contribute directly to troubleshooting efforts required for laboratory instrumentation.
  • Communicate effectively with other team members and teams regarding the generated analytical data.

STAKEHOLDER INTERACTION

  • Type of Interaction: Internal
  • Interaction with: Other team members and teams.
  • Nature of Interaction: Communicate effectively regarding the analytical data.
  • Type of Interaction: External
  • Interaction with: Not explicitly specified in the vacancy details.
  • Nature of Interaction: Not explicitly specified in the vacancy details.

JOB REQUIREMENTS

Professional Experience and Relevant Skills

Experience: 2-5 years of experience within an analytical development laboratory setting.

Skills:

  • Hands-on experience in HPLC and UPLC is mandatory. Knowledge and hands-on experience of different chromatography modes like RP, HIC, IEX, SEC, etc., is required.
  • Knowledge and hands-on experience of different capillary electrophoresis techniques (CIEF, CZE, CE-SDS, etc.) is required. Hands-on experience with Higher order structure analysis (DSC, CD, Fluorescence, FTIR, etc.) is an advantage.
  • Technical Expertise: Experience working on biotherapeutic proteins like monoclonal antibodies, Fc fusion, peptibody, or any candidate biosimilars is required. Method Development and Qualification experience is a must. An understanding of analytical deliverables involving CQA, QTPP, Analytical similarity, Forced degradation studies, and Specifications setting is preferred.

Academic Qualifications & Certifications:

Educational Qualification: BSc./MSc. Biotechnology or B.Tech/Mtech. Biotechnology

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