MANAGER

Panacea Biotec Limited

India

On-site

INR 1,800,000 - 3,200,000

Full time

14 days+

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Job summary

Panaceabiotec, Lalru R&D, seeks a Senior Scientist in vaccine formulation analytics. You will develop and validate assays for vaccine characterization, manage technology transfer, and ensure compliance with GLP standards across cross-functional teams.

Responsibilities include coordinating with formulation, QC, QA, and regulatory affairs to meet project timelines and prepare regulatory documentation for submissions.

Qualifications

  • Demonstrated experience in the development of assays for vaccine characterization, release and stability testing.
  • In-depth knowledge of biochemical, immunochemical, cell-based, and chromatography-based analytical methods.
  • Strong scientific and technical skills to analyze results and troubleshoot assays.

Responsibilities

  • Identify and evaluate new products/technologies/analytical methods aligned with company goals.
  • Develop, optimize and validate analytical methods for vaccine products for regulated, WHO and domestic markets.
  • Coordinate with Formulation, Material Management, Quality Control, QA, and Regulatory Affairs to meet timelines.
  • Prepare and review documents for technology transfer and regulatory filing such as development reports and SOPs.

Skills

Vaccine assay development
Analytical method validation
GLP knowledge
Data analysis
Documentation & reporting
Cross-functional collaboration

Education

PhD/MSc/Ph.D. in Biotechnology/Biochemistry/Life Sciences

Job description

12 - 15 Years

PERMANENT

Job Description

Reporting to : Senior General Manager-Vaccine FormulationResearch

Nature of Position : Permanent

Number of Positions : One

Educational Qualification : Phd/M.Sc.Ph.D. in Biotechnology / Biochemistry / Life Sciences from a reputed institute

  • 1. Identify, propose and evaluatepotential new products/technologies/analytical methodologies that align withthe company's vision and goals.
  • 2. Develop, optimize and validateanalytical methods for new and existing vaccine products to meet therequirements of Regulated, WHO, and Domestic markets.
  • 3. Ensure successful technologytransfer and demonstration of analytical methods to Quality Control teams atmanufacturing sites.
  • 4. Co-ordinate withcross-functional teams including Formulation, Material Management, QualityControl, Quality Assurance, and Regulatory Affairs to achieve projecttimelines.
  • 5. Responsible for preparationand review of documents for technology transfer and regulatory filing such asdevelopment report, analytical method validation report/ protocol, SOPs, STPs
  • 6. Perform and ensure allexperimental procedures are conducted in compliance with Good LaboratoryPractices (GLP) guidelines ensuring regular documentation.
  • 7. Ensure timely preparation,review, and submission of analytical test reports for product release,maintaining data traceability and authenticity.
  • 8. Undertake analytical testingand allocate routine and stability samples to analysts for timely completion oftesting activities.
  • 9. Maintain records of reagents,raw materials, and consumables required for various projects and initiateprocurement requests to ensure smooth lab operations.
  • 10. Ensure upkeep, calibration, and preventive maintenanceof laboratory instruments.
  • 11. Prepare and report progress of assigned projects tosuperiors.
  • 12. Undertake any other project-related responsibilitiesor tasks assigned by reporting managers.
Skill Requirements
  • 1. Must have demonstratedexperience in the development of assays for Vaccine characterization, releaseand stability testing.
  • 2. In-depth knowledge andunderstanding of biochemical, immunochemical, cell-based, andchromatography-based analytical methods and possess strong scientific &technical skills.
  • 3. Thoroughly analyze results andmethods, solve analytical problems, and troubleshoot assays.
  • 4. Understanding and practicalknowledge of GLPs as applied to analytical requirements.
  • 5. Strong interpersonal skills;ability to communicate effectively both verbally and in written formats.
  • 6. Self-starter; ability to workin a fast-paced, cross-functional environment and collaborate effectively withother team members.
Job Snapshot
Updated Date

30-07-2026

Job ID

JOB_1161

LALRU R&D (SAMPANN)

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