Looking for Analytical Scientist jobs in Hyderabad? Azurity Pharmaceuticals is hiring Analytical Scientist/Scientist professionals for its Research & Development (Analytical R&D) team in Hyderabad. This opportunity is ideal for M.Pharm and M.Sc graduates with experience in Analytical Method Development, LCMS, Nitrosamine Impurity Analysis, HPLC, Stability Studies, and Pharmaceutical R&D.

If you have hands-on experience in Analytical Research & Development, impurity profiling, analytical method validation, and pharmaceutical laboratory operations, this is an excellent opportunity to join a rapidly growing global specialty pharmaceutical company focused on improving patient outcomes.

About Azurity Pharmaceuticals

Azurity Pharmaceuticals is a leading specialty pharmaceutical company dedicated to developing innovative medicines for underserved patient populations. The company offers a broad portfolio of products across cardiovascular, neurology, endocrinology, gastroenterology, institutional, and orphan disease therapeutic areas.

With strong R&D capabilities and a patient-first approach, Azurity continues to expand its global pharmaceutical pipeline through scientific innovation and quality-driven research.

Job Details

Key Responsibilities

Selected candidates will be responsible for:

• Perform analytical method development for Nitrosamine impurities.
• Develop and validate analytical methods using LCMS.
• Identify unknown and genotoxic impurities using LCMS.
• Operate HPLC-PDA, UV, ELSD, and LCMS instruments.
• Analyze formulation development samples.
• Perform stability sample analysis.
• Execute compendial method verification.
• Prepare analytical reports and laboratory documentation.
• Maintain Good Documentation Practices (GDP).
• Ensure compliance with Good Laboratory Practices (GLP).
• Follow SOPs and Data Integrity guidelines.
• Prepare STP, MDR, and MOA documentation.
• Maintain calibration and qualification of analytical instruments.
• Support formulation development through analytical testing.
• Ensure laboratory safety and regulatory compliance.

Eligibility Criteria

Candidates should possess:

• Postgraduate degree in Pharmacy (M.Pharm) or Science (M.Sc).
• Minimum 3 years of Analytical R&D experience.
• Strong expertise in LCMS operation.
• Experience in Nitrosamine impurity method development.
• Knowledge of unknown impurity identification.
• Hands-on experience with:
  • HPLC
  • PDA
  • UV
  • ELSD
  • LCMS
• Understanding of GLP, GDP, and Data Integrity.
• Exposure to electronic Laboratory Notebook (eLN) and DMS systems.
• Good written and verbal communication skills.

Preferred Skills

• Analytical Method Development
• Method Validation
• Pharmaceutical Analytical R&D
• LCMS Analysis
• Nitrosamine Impurity Analysis
• Stability Studies
• Compendial Method Verification
• Documentation Practices
• Pharmaceutical Research
• Regulatory Compliance
• Instrument Calibration
• Pharmaceutical Laboratory Operations

Why Join Azurity Pharmaceuticals?

Employees can expect:

• Opportunity to work with advanced analytical technologies.
• Exposure to global pharmaceutical R&D projects.
• Collaborative scientific environment.
• Career growth in Analytical Research.
• Learning opportunities in impurity profiling and advanced analytical techniques.
• Competitive salary and employee benefits.
• Inclusive workplace and equal opportunity employer.

Salary (Expected)

Based on current Pharmaceutical Analytical R&D market standards in Hyderabad:

₹8,00,000 – ₹13,00,000 per annum (CTC)

Actual salary may vary depending on experience, skills, and company evaluation.

Who Can Apply?

Eligible candidates include:

• M.Pharm
• M.Sc (Chemistry/Analytical Chemistry/Relevant Sciences)

Candidates should have at least 3 years of Pharmaceutical Analytical R&D experience, particularly in LCMS-based analytical method development.

Location

Hyderabad, Telangana, India

How to Apply?

Application Link