Aurigene Oncology Hiring– Scientist / Sr. Scientist – Analytical Research & Development | Bangalore

Aurigene Oncology, a leading oncology-focused pharmaceutical organization, has announced an exciting career opportunity for experienced professionals in Analytical Research & Development (AR&D). The company is looking for talented candidates for the position of Scientist / Senior Scientist – Analytical R&D at its Bangalore location.

This opportunity is ideal for professionals with strong expertise in analytical method development, validation, stability studies, characterization techniques, and regulatory compliance within the pharmaceutical industry.

Job Overview

Particulars Details

Company Name

Aurigene Oncology

Position

Scientist / Sr. Scientist – Analytical Research & Development

Location

Bangalore

Qualification

M.Pharm / M.Sc Chemistry / Ph.D

Experience

M.Pharm/M.Sc: 12–15 Years, Ph.D: 6–8 Years

Department

Analytical Research & Development (AR&D)

Industry

Pharmaceutical / Oncology

Employment Type

Full-Time

Desired Candidate Profile

Candidates should possess:

M.Pharm or M.Sc in Chemistry with 12–15 years of relevant pharmaceutical experience.

Ph.D candidates with 6–8 years of industrial experience can also apply.

Strong knowledge of analytical method development and validation.

Experience in handling complex formulations including liposomal and nano-suspension products.

Leadership experience in managing analytical teams.

Key Responsibilities

The selected candidate will be responsible for:

1. Team Leadership

Lead, mentor, and manage a team of approximately 5–7 analytical scientists.

Drive technical excellence and project execution within the analytical department.

2. Method Development & Validation

Oversee analytical method development, validation, and transfer activities.

Support Oral Solid Dosage (OSD), Injectables, and Long-Acting Formulations.

3. Stability Studies

Design, execute, and monitor stability studies.

Ensure compliance with global regulatory guidelines and stability protocols.

4. Advanced Analytical Characterization

Perform and interpret data using:

Spectroscopic techniques

PXRD (Powder X-Ray Diffraction)

DSC (Differential Scanning Calorimetry)

TGA (Thermogravimetric Analysis)

Zetasizer

Other physical characterization instruments

5. GLP & Regulatory Compliance

Maintain Good Laboratory Practices (GLP).

Ensure audit readiness and laboratory compliance.

Support regulatory inspections and documentation.

6. Quality Management System (QMS)

Manage and execute:

Investigations

Deviations

Change Controls

CAPA (Corrective and Preventive Actions)

7. Training & Development

Conduct technical training programs.

Train team members on SOPs, STPs, analytical instruments, and laboratory practices.

8. Vendor & External Laboratory Coordination

Coordinate with vendors, auditors, and contract testing laboratories.

Manage outsourced analytical testing and compliance activities.

Why Join Aurigene Oncology?

Opportunity to work in cutting-edge oncology research.

Exposure to advanced analytical technologies.

Leadership role with high-impact projects.

Collaborative and innovation-driven work environment.

Strong focus on diversity and equal opportunities.

How to Apply?

Interested candidates can send their updated resume to:

sushmitha@aurigene.com

rajesh_m@aurigene.com

Location: Bangalore

Technical FAQs

1. What is analytical method validation in pharmaceutical R&D?

Analytical method validation is the documented process of proving that an analytical method is suitable for its intended purpose. It includes parameters such as accuracy, precision, specificity, linearity, robustness, detection limit, and quantitation limit as per ICH guidelines.

2. What is the significance of PXRD in pharmaceutical development?

PXRD (Powder X-Ray Diffraction) is used to identify crystalline forms, polymorphism, and material characteristics of APIs and formulations. It helps ensure product stability and performance.

3. Why is a Zetasizer used in liposomal and nano-suspension formulations?

A Zetasizer measures particle size, zeta potential, and molecular weight. These parameters are critical for assessing stability, uniformity, and performance of liposomal and nano-suspension drug products.

4. What is the role of CAPA in Quality Management Systems?

CAPA (Corrective and Preventive Action) helps identify root causes of quality issues, implement corrective measures, and prevent recurrence, ensuring continuous quality improvement and regulatory compliance.

5. What are DSC and TGA used for in pharmaceutical characterization?

DSC (Differential Scanning Calorimetry): Evaluates thermal properties such as melting point and glass transition temperature.

TGA (Thermogravimetric Analysis): Measures weight changes due to temperature variation, helping determine moisture content and thermal stability.