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    Pharma Freshers Job Opening | Hetero hiring Chemist Role | B Pharmacy Graduates | Apply Now

    Hetero Hiring Chemist Role | Pharma Freshers Job | B Pharmacy Graduates | Apply Now

    Looking for a Pharma Freshers Job in the pharmaceutical industry? Hetero has announced exciting Hetero Careers opportunities for the Chemist role at its API division in Andhra Pradesh. This Pharma Freshers Job is ideal for candidates with qualifications in Analytical Chemistry, Organic Chemistry, or B Pharma who are looking to build a successful career in Quality Control and analytical testing within a leading pharmaceutical company.

    • Position: Chemist
    • Location: Andhra Pradesh

    About the Company

    Hetero is one of India’s leading pharmaceutical companies with a strong presence in APIs, generics, and pharmaceutical manufacturing. Hetero Careers provide excellent opportunities for freshers and experienced professionals in pharmaceutical production, quality control, and research domains.

    Key Responsibilities

    Sampling and Analysis

    • Perform sampling of raw materials, intermediates, and finished Active Pharmaceutical Ingredients (APIs) according to standard procedures.
    • Conduct routine and non-routine chemical and physical tests to ensure quality standards are met.
    • Analyze products using techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), UV-Vis spectroscopy, FTIR, and other analytical instruments.

    Documentation

    • Accurately document all analytical results and observations in laboratory notebooks or electronic systems.
    • Prepare and review certificates of analysis (CoA) for finished products and intermediates.
    • Ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) in all documentation.

    Compliance and Standards

    • Adhere to established quality standards as per pharmacopeias (USP, BP, IP, EP, etc.) and regulatory guidelines.
    • Ensure that all QC activities comply with regulatory and company standards, including FDA, ICH, and WHO requirements.
    • Participate in internal and external audits and implement corrective actions where required.

    Instrument Calibration and Maintenance

    • Perform regular calibration, qualification, and preventive maintenance of laboratory equipment.
    • Troubleshoot and resolve instrument issues in collaboration with the maintenance or engineering team.

    Stability Studies

    • Conduct stability studies for APIs to determine shelf life and storage conditions.
    • Monitor and report stability data as per ICH guidelines.

    Deviations and Investigations

    • Identify and report deviations or out-of-specification (OOS) results.
    • Participate in root cause analysis and provide recommendations for corrective and preventive actions (CAPA).

    Method Development and Validation

    • Assist in the development, optimization, and validation of analytical methods for new APIs.
    • Support the transfer of validated methods to production and QC teams.

    Training and Knowledge Sharing

    • Train junior staff on QC procedures, analytical techniques, and safety protocols.
    • Stay updated on new analytical methods, regulatory requirements, and quality standards.

    Qualifications

    Education

    • B.Pharmacy

    Technical Skills

    • Proficiency in analytical techniques such as HPLC, GC, UV-Vis, FTIR, and titration
    • Familiarity with laboratory software such as Chromeleon, LabSolutions, or Empower
    • Understanding of GMP, GLP, and regulatory requirements

    Soft Skills

    • Strong analytical and problem-solving abilities
    • Attention to detail and commitment to quality
    • Effective communication and documentation skills

    Work Environment

    • Laboratory-based role with exposure to chemicals and analytical equipment
    • May require flexible working hours to meet project deadlines or address critical issues

    Key Performance Indicators (KPIs)

    • Accuracy and reliability of analytical results
    • Timely completion of testing and reporting
    • Compliance with GMP/GLP and audit readiness
    • Effective resolution of OOS and deviations

    CLICK HERE FOR ORIGINAL NOTIFICATION

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