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Research Assistant – Ar&D

Piramal Pharma
Piramal Pharma
1-4 years
3-5 LPA
Telangana
10 May 6, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Research Assistant – AR&D
Location: Digwal, Telangana, India
Company: Piramal Pharma Solutions
Job Type: Full-Time
Experience Required: 1–4 Years
Application Deadline: 9 May 2026


About Piramal Pharma Solutions

Piramal Pharma Solutions is a globally recognized Contract Development and Manufacturing Organization (CDMO) delivering end-to-end pharmaceutical development and manufacturing solutions across the complete drug lifecycle.

With a strong international presence across North America, Europe, and Asia, the organization supports pharmaceutical and biotechnology companies through services including:

  • Drug Discovery Solutions

  • Process & Pharmaceutical Development

  • Clinical Trial Supplies

  • API Manufacturing

  • Finished Dosage Form Manufacturing

  • Highly Potent API Development

  • Antibody Drug Conjugation Services

The company works with both innovator and generic pharmaceutical organizations worldwide using advanced scientific technologies and integrated manufacturing capabilities.


Job Opening: Research Assistant – AR&D

Job Overview

Piramal Pharma Solutions is hiring experienced professionals for the role of Research Assistant – AR&D (Analytical Research & Development). The selected candidate will be responsible for analytical method development, method validation, wet lab analysis, instrument calibration, troubleshooting, stability sample analysis, laboratory documentation, and regulatory-compliant analytical operations.

This opportunity is ideal for candidates with hands-on experience in analytical instruments such as HPLC, GC, KF, UV, IR, Potentiometer, and Polarimeter within pharmaceutical analytical laboratories.


Key Responsibilities

Analytical Method Development & Validation

  • Perform analytical method development and validation using HPLC, GC, KF, Potentiometer, and other analytical instruments.

  • Prepare analytical method validation protocols and reports.

  • Develop specifications, STPs, calibration schedules, and analytical reports.

Instrument Handling & Calibration

  • Operate, calibrate, maintain, and troubleshoot instruments including:

    • HPLC

    • GC

    • Karl Fischer (KF)

    • UV Spectrophotometer

    • IR Spectrometer

    • Potentiometer

    • Polarimeter

    • Oven

    • Melting Range Apparatus

  • Review calibration data and maintain compliance records.

Sample Analysis & Wet Lab Activities

  • Perform analysis of project samples using advanced analytical techniques.

  • Conduct wet chemistry analysis including:

    • Water content analysis

    • Titrations

    • ROI testing

  • Analyze stability samples and hold-time study samples.

Documentation & Compliance

  • Maintain online laboratory documentation and audit-ready records.

  • Manage:

    • Instrument usage logs

    • Column usage records

    • Standard usage records

  • Prepare quality and compliance documents such as:

    • Change Annexures

    • QRA

    • CCF

    • Laboratory Incidence Reports

Reference Standards & Laboratory Maintenance

  • Maintain and qualify reference standards as per SOPs.

  • Prepare reagents and standardize volumetric solutions.

  • Ensure laboratory cleanliness, safety compliance, and audit readiness at all times.

Safety & GMP Compliance

  • Follow laboratory safety protocols and GMP practices.

  • Use PPE including:

    • Safety goggles

    • Gloves

    • Lab coats


Required Skills

  • Analytical Method Development

  • Method Validation

  • HPLC Handling & Troubleshooting

  • GC Analysis

  • Karl Fischer Titration

  • Wet Lab Analysis

  • Calibration & Qualification

  • Pharmaceutical Documentation

  • Stability Studies

  • GMP & GLP Compliance


Eligibility Criteria

Educational Qualification

  • B.Pharm

  • M.Pharm

  • MSc Chemistry

  • Pharmaceutical Sciences or related discipline

Experience

  • 1–4 years of relevant experience in AR&D, Analytical Laboratory, or Pharmaceutical R&D environments.


Why Join Piramal Pharma Solutions?

  • Work with a globally established pharmaceutical CDMO

  • Exposure to international pharmaceutical projects

  • Advanced analytical laboratory environment

  • Career growth opportunities in Analytical R&D

  • Hands-on experience with regulated pharmaceutical operations


How to Apply

Interested candidates can apply directly through the official career portal of Piramal Pharma Solutions before the application deadline.

For more global pharmaceutical, clinical research, pharmacovigilance, regulatory affairs, and biotechnology job updates, visit ThePharmaDaily.