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Formulation Analytical Reaearch & Development

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Onsite

Formulation Analytical Reaearch & Development

Hetero

Formulation Analytical Reaearch & Development

Skills

Compliance

1 month ago

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Important information


Contract type:

Permanent

Location:

Hyderabad, Telangana, India

Work mode:

Onsite

Published on:

20 September 2026

What they need


Job Summary

The Trainee Research Associate will support analytical activities related to formulation development projects. The candidate will be involved in routine analysis, analytical method development, method validation, stability sample testing, and documentation in compliance with GMP, GLP, and regulatory requirements.

Qualification

  • M.Pharm / MS Pharm (Pharmaceutical Analysis)
  • Freshers (2025/2026 Pass-outs)

Key Responsibilities

Analytical Activities

  • Perform analysis of raw materials, in-process samples, finished products, and stability samples.
  • Operate and maintain analytical instruments such as HPLC, UPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, and KF Titrator.
  • Support analytical method development and method validation activities.
  • Execute routine testing as per approved analytical procedures and specifications.
  • Assist in troubleshooting analytical issues during product development.

Documentation

  • Maintain laboratory notebooks, raw data, analytical worksheets, and instrument logbooks.
  • Prepare analytical reports and data summaries.
  • Ensure compliance with Good Documentation Practices (GDP).

Stability Studies

  • Analyze stability samples as per approved protocols.
  • Record and report analytical observations accurately.
  • Support shelf-life determination studies for pharmaceutical products.

Compliance Quality

  • Follow cGMP, GLP, Data Integrity, and laboratory safety requirements.
  • Ensure proper handling and disposal of chemicals and laboratory waste.
  • Participate in laboratory audits and compliance activities.

Cross-Functional Coordination

  • Coordinate with Formulation Development, Quality Control, and Regulatory Affairs teams.
  • Support technology transfer and scale-up activities whenever required.

Required Skills

  • Basic knowledge of pharmaceutical analytical techniques.
  • Understanding of HPLC, UV, Dissolution, and chromatographic principles.
  • Knowledge of ICH guidelines and analytical method validation concepts.
  • Good laboratory practices and documentation skills.
  • Strong analytical and problem-solving abilities.
  • Effective communication and teamwork skills.

Preferred Competencies

  • Exposure to pharmaceutical laboratory equipment during academics or project work.
  • Knowledge of Microsoft Excel, Word, and PowerPoint.
  • Ability to learn and adapt in a fast-paced RD environment.

Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

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