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    Job · 18400816

    HYDERABAD · FULLTIME

    Formulation Analytical Reaearch & Development

    Hetero logo

    Hetero

    Hyderabad · onsite · Posted 33d ago

    Sourced fromNaukri
    Undisclosed4–8 yrsfulltimeHyderabad

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    Section · 01

    About this role

    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.

    Sourced from naukri

    Section · 02

    Skills

    CGMPAnalytical Method ValidationAnalytical Method Developmentanalytical reportsfinished productsftirauditsMethod ValidationHPLCFormulation DevelopmentChemicalscomplianceLaboratory EquipmentPharmaceutical

    Section · Company

    About Hetero

    Hetero logo

    Hetero

    Pharma

    3.2k+

    employees

    1993

    33 years old

    Hyderabad/Secunderabad, Telangana

    India

    About

    One of the world’s leading producers of key Active Pharmaceutical Ingredients and generic formulations with a presence in 140+ countries and backed by 30 years of experience in the pharma sectors.

    Industries

    PharmaHealthcare / PharmaClinical ResearchHealthcare

    Employee ratings

    4,524 reviews

    3.9/ 5

    Culture

    3.6

    Career growth

    3.3

    Work-life

    3.8

    Employees rate it well for

    Salary404Work Culture302Work Environment287Learning287Senior Management234

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