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Research Associate – Ar&D

Piramal Pharma
2-5 years
preferred by company
Digwal, Telangana, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Research Associate – AR&D (Analytical Research & Development)

Location: Digwal, Telangana, India
Job Type: Full-Time
Work Mode: Onsite
Industry: Pharmaceutical | Analytical Research & Development | API | CDMO | Life Sciences
Experience Required: 2–5 Years (Freshers May Not Be Preferred)
Job Reference ID: R00001659
Application Deadline: May 20, 2026

Job Overview

A leading global Contract Development and Manufacturing Organization (CDMO) is hiring a Research Associate – Analytical Research & Development (AR&D) for its Digwal, Telangana facility. This opportunity is ideal for professionals with strong expertise in analytical chemistry, pharmaceutical method development, HPLC, GC, wet analysis, API stability testing, and GLP compliance.

The role is suited for analytical professionals who can independently manage laboratory projects, support pharmaceutical development teams, perform method validation activities, and ensure compliance with regulated laboratory quality standards.

This is an excellent opportunity for candidates seeking growth in pharmaceutical R&D, API analytical development, quality-controlled laboratory environments, and regulated manufacturing operations.

About the Organization

The hiring organization is a globally recognized pharmaceutical development and manufacturing company specializing in drug discovery, pharmaceutical development, clinical trial supply, API manufacturing, finished dosage forms, highly potent compounds, and advanced pharmaceutical solutions.

With operations across North America, Europe, and Asia, the organization serves both innovator and generic pharmaceutical companies worldwide.

Key Responsibilities

Analytical Testing & Method Development

  • Perform analytical testing in support of pharmaceutical development and synthetic research teams.
  • Independently manage assigned analytical research projects.
  • Execute analytical method development, method optimization, and routine testing activities.
  • Support troubleshooting of analytical methods and laboratory investigations.

Instrument Handling & Laboratory Operations

  • Operate and maintain analytical instruments including:
    • High Performance Liquid Chromatography (HPLC)
    • Gas Chromatography (GC)
    • Potentiometer
    • Polarimeter
    • Wet chemistry analysis equipment
  • Perform instrument calibration as per master calibration schedules.
  • Maintain instrument logs, laboratory journals, and digital documentation.

Quality Compliance & Documentation

  • Coordinate with Quality Assurance teams for:
    • Method transfer activities
    • Change control documentation
    • Investigation report support
    • Compliance documentation
  • Ensure adherence to:
    • Good Laboratory Practices (GLP)
    • Standard Operating Procedures (SOPs)
    • 21 CFR Part 11 compliance standards
    • Hazardous chemical handling regulations

API Stability & Pharmaceutical Development Support

  • Support API stability studies and analytical monitoring.
  • Assist pharmaceutical development teams with analytical research requirements.
  • Ensure reagent preparation, standardization of volumetric solutions, and laboratory inventory readiness.

Safety & Environmental Compliance

  • Maintain laboratory cleanliness and controlled environmental conditions.
  • Follow safety protocols related to hazardous chemical handling.
  • Identify unsafe acts or conditions and initiate corrective and preventive actions.
  • Ensure compliance with waste disposal and environmental safety practices.

Required Qualifications

Educational Requirements

  • Bachelor’s or Master’s Degree in Chemistry, Pharmaceutical Chemistry, Analytical Chemistry, Pharmacy, or related life sciences discipline

Experience Requirements

  • 2–5 years of relevant experience in AR&D, pharmaceutical analytical laboratories, API development, or quality-controlled research environments
  • Freshers with strong academic analytical laboratory exposure may be considered depending on organizational requirements

Required Skills

  • HPLC Analysis
  • Gas Chromatography (GC)
  • Wet Chemistry Analysis
  • Analytical Method Development
  • Method Transfer
  • API Stability Testing
  • GLP Compliance
  • 21 CFR Part 11
  • SOP Compliance
  • QA Coordination
  • Laboratory Documentation
  • Instrument Calibration
  • Investigation Support
  • Chemical Safety Management
  • Pharmaceutical Analytical Testing