Associate Scientist - Analytical Development (Biopharma)

Intas Pharmaceuticals; Ahmedabad District; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Intas Pharmaceuticals seeks an ADL Associate to deliver high-quality analytical data for biotherapeutic product development. You will execute methods like chromatography and electrophoresis, develop and qualify assays, and support regulatory-compliant documentation.

The role requires 4–8 years of hands-on biopharmaceutical analytics, strong data interpretation, and clear technical communication, working within a GLP-oriented lab environment.

Qualifications

• M. Sc. or M. Tech. in Biochemistry/Biotechnology required.
• 4–8 years hands-on biopharmaceutical/analytical development experience.
• Expertise in chromatographic and electrophoretic methods as listed.

Responsibilities

• Timely execution of analytical deliverables for biotherapeutic projects involving QTPP, process support, method development, qualification, and transfer.
• Prepare and review SOPs, MOAs, MDRs, and other technical documentation.

Skills

Chromatography

Electrophoretic methods

N-Glycan analysis

Higher-order structure analysis

Analytical method development

MS Office

Documentation and communication

Education

M. Sc. or M. Tech. - Biochemistry or Biotechnology

Tools

HPLC/UPLC systems

Analytical instruments software

Job description

The ADL Associate responsible for delivering high-quality analytical data to support biotherapeutic product development. The role involves hands-on execution of various analytical techniques including chromatography and electrophoresis, with a focus on method development, qualification, and process support, ensuring compliance with regulatory and scientific standards.

Key Responsibility:

• Timely execution of analytical deliverables for biotherapeutic projects involving QTPP, process support, method development, qualification, and transfer.
• Perform benchwork using diverse analytical techniques including colorimetric/spectrophotometric assays, chromatographic tests (SEC, IEX, HIC, RP), and electrophoresis (cIEF, CE-SDS NR & R, CE-LIF).
• Independently plan, execute, and interpret experiments with sound scientific judgment.
• Maintain accurate and timely documentation of all experimental results, protocols, and reports.
• Prepare and review SOPs, MOAs, MDRs, and other technical documentation.
• Ensure adherence to Good Laboratory Practices (GLP) and assist in maintaining lab discipline and documentation systems.
• Support project teams with scientific input, report preparation, and presentations.

Skills and Competencies:

• Expertise in chromatographic techniques (SEC, IEX, HIC, RP) using HPLC/UPLC systems.
• Proficiency in electrophoretic methods such as cIEF, CE-SDS (Non-reducing & Reducing), CE-LIF.
• Hands-on experience in N-Glycan analysis and higher-order structure analysis is an advantage.
• Strong understanding of analytical method development and validation for biotherapeutics.
• Proficiency in MS Office and software tools linked to analytical instruments.
• Strong documentation and communication skills.

Educational Qualifications:

• M. Sc. or M. Tech. - Biochemistry or Biotechnology

Preferred Experience:

• 4 – 8 years of hands-on experience in a biopharmaceutical or analytical development environment.