India's DMPLOI - Jobs & Networking AppAurigene Oncology, a leading innovation-driven pharmaceutical and oncology research organization, has announced an exciting career opportunity for experienced professionals in Analytical Research & Development (AR&D). The company is seeking talented candidates for the position of Scientist / Senior Scientist – Analytical Research & Development at its Bangalore facility.
This opportunity is ideal for analytical scientists with extensive experience in pharmaceutical research, method development, stability studies, and advanced characterization techniques, particularly in oncology and complex formulations.
About the Position
The selected candidate will play a critical role in leading analytical research activities, managing scientific teams, and ensuring compliance with global regulatory standards. The role demands strong expertise in analytical method development, validation, technology transfer, and quality systems management.
Position
Scientist / Sr. Scientist – Analytical Research & Development
Location
Bangalore, Karnataka
Educational Qualification & Experience
Candidates should possess:
M.Pharm or M.Sc in Chemistry with 12–15 years of relevant experience, OR
Ph.D. with 6–8 years of relevant industry experience.
Key Responsibilities
The selected professional will be responsible for:
Leading and mentoring a team of approximately 5–7 analytical scientists.
Managing analytical method development, validation, and transfer activities for:
Oral Solid Dosage (OSD)
Injectable formulations
Long-acting formulations
Liposomal products
Nano-suspensions
Designing and monitoring stability studies as per global regulatory requirements.
Performing advanced analytical characterization using:
Spectroscopic techniques
PXRD
DSC
TGA
Zetasizer
Other physical characterization instruments
Ensuring compliance with Good Laboratory Practices (GLP).
Managing Quality Management System (QMS) activities including:
Deviations
Investigations
Change controls
CAPA management
Conducting technical training sessions on analytical instrumentation and laboratory procedures.
Coordinating with external laboratories, auditors, and vendors for analytical testing and compliance activities.
Why Join Aurigene Oncology?
Aurigene Oncology is recognized for its commitment to advancing cancer treatment through scientific innovation. Employees get the opportunity to work on cutting-edge pharmaceutical technologies, complex formulations, and globally regulated projects while collaborating with highly skilled scientific teams.
The organization also promotes diversity, equal opportunity, and a culture of continuous learning and professional growth.
How to Apply
Interested and eligible candidates can send their updated resume to:
sushmitha@aurigene.com
rajesh_m@aurigene.com
Applicants are encouraged to highlight their expertise in analytical method development, regulatory compliance, stability studies, and advanced characterization techniques.
Technical FAQs
1. What is analytical method validation in pharmaceutical R&D?
Analytical method validation is the documented process of proving that an analytical procedure is suitable for its intended purpose. Parameters typically evaluated include accuracy, precision, specificity, linearity, robustness, detection limit, and quantitation limit as per ICH guidelines.
2. What is the significance of PXRD in pharmaceutical analysis?
Powder X-Ray Diffraction (PXRD) is used to identify crystalline forms, polymorphism, and structural changes in pharmaceutical compounds. It is especially important for understanding drug stability and formulation performance.
3. Why is Zeta Potential analysis important for nano-suspensions and liposomal formulations?
Zeta Potential measurement helps determine the surface charge and stability of dispersed particles. Higher absolute zeta potential values generally indicate better physical stability and reduced particle aggregation.
4. What role do DSC and TGA play in formulation development?
Differential Scanning Calorimetry (DSC) evaluates thermal transitions such as melting points and glass transition temperatures, while Thermogravimetric Analysis (TGA) measures weight changes due to moisture loss, degradation, or decomposition, helping assess product stability.
5. What are CAPA activities within a pharmaceutical Quality Management System?
CAPA (Corrective and Preventive Action) is a systematic approach used to identify root causes of deviations, implement corrective measures, prevent recurrence, and continuously improve quality and compliance within pharmaceutical operations.
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