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Senior Scientist

Biocon Biologics
4-6 years
Not Disclosed
PAN-India, India
1 June 4, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

Job Title: Senior Scientist (Analytical R&D)

Requisition ID: 20768
Company: Biocon Pharma Limited
Department: Analytical Research & Development
Location: India
Experience Required: 4–8 Years
Education: M.Pharm (Mandatory)


Role Overview

The Senior Scientist – Analytical R&D is responsible for planning, executing, and delivering analytical development activities to support formulation and product development. The role focuses on method development, validation, technology transfer, and ensuring compliance with regulatory and quality standards in a pharmaceutical R&D environment.

The position requires close collaboration with formulation teams, manufacturing sites, and external research organizations to ensure timely and high-quality analytical support for drug development projects.


Key Responsibilities

1. Analytical Method Development

  • Develop and qualify analytical methods to support formulation and product development

  • Apply Quality by Design (QbD) principles in method development

  • Ensure robust, reliable, and reproducible analytical procedures

2. Project Execution & Planning

  • Plan and execute daily analytical R&D activities as per project requirements

  • Ensure timely completion of assigned tasks with high quality standards

  • Participate actively in technical discussions and project planning

3. Regulatory & Compliance

  • Ensure compliance with GLP (Good Laboratory Practices) and laboratory safety standards

  • Maintain adherence to departmental SOPs and quality systems

  • Ensure documentation accuracy and regulatory readiness

4. Technology Transfer

  • Transfer analytical methods to manufacturing sites for routine release testing

  • Support both internal and external manufacturing sites during transfer activities

  • Ensure smooth transition and validation of analytical procedures

5. Cross-Functional Collaboration

  • Work closely with formulation development and other cross-functional teams

  • Understand project requirements and provide analytical support accordingly

  • Contribute to scientific and technical discussions for project advancement

6. Outsourced & CRO Coordination

  • Coordinate analytical development activities with Contract Research Organizations (CROs)

  • Monitor outsourced project progress and ensure quality deliverables

7. Laboratory Management

  • Maintain inventory of chemicals, solvents, and analytical consumables

  • Support procurement, installation, and qualification of analytical instruments

  • Ensure efficient laboratory operations and resource availability

8. Stability & Data Analysis

  • Plan and monitor stability studies for assigned projects

  • Compile, analyze, and track stability data trends

  • Ensure accurate reporting and documentation of results

9. Quality & Efficiency

  • Ensure high efficiency and timely delivery of analytical activities

  • Maintain data integrity and scientific accuracy in all outputs

  • Support continuous improvement initiatives within the department


Required Qualifications

Education

  • M.Pharm (Master of Pharmacy) – Mandatory

Experience

  • 4 to 8 years of experience in Analytical R&D or related pharmaceutical development roles