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    Job · 18776035

    BDR Pharmaceuticals International logo

    Walk-in || ADL - Officer / Executive

    BDR Pharmaceuticals International · Not specified · onsite · Posted 30d ago

    Undisclosed2–6 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    ADL - Query and Characterization

    To perform advanced analytical method development and characterization for complex dosage forms (injectable, lyophilized products, depots, peptides, and oral solids), and to effectively handle regulatory queries from global markets in compliance with international guidelines.

    • Perform method development, optimization, and troubleshooting for:
      • Injectables, lyophilized formulations, depot formulations, peptides, and OSDs
    • Conduct advanced characterization using instruments such as:
      • DSC (Differential Scanning Calorimetry)
      • XRD (X-ray Diffraction)
      • NMR (Nuclear Magnetic Resonance)
      • IC (Ion Chromatography)
      • ICP-OES (Inductively Coupled Plasma Optical Emission Spectroscopy)


    ADL - Documentation Review

    • Responsible for preparation and reviewing of Specification, Method of analysis,raw material, in process, finished product and other documents.
    • Responsibility of preparing & reviewing vendor qualification & Tech Transfer documents.
    • Responsibility of maintaining Analytical Documents & records.
    • Responsible for preparation of study reports, nitrosamine, elemental, residual solvent,genotoxic .
    • Daily and monthly calibration of instrument.
    • Responsible for maintaining analytical chemicals, solvents, analytical standard and chromatographic columns within the laboratory.


    ADL - MS&T

    Technology Transfer

    • Lead or support transfer of analytical methods from R&D/ADL to QC labs or manufacturing sites
    • Prepare and review Tech Transfer Protocols (TTP) and reports
    • Coordinate with cross-functional teams (R&D, QA, QC, Production)

    2. Analytical Method Support

    • Perform method validation, verification, and troubleshooting
    • Ensure methods comply with regulatory standards like ICH guidelines
    • Handle instruments like HPLC, GC, UV, dissolution apparatus

    3. Documentation & Compliance

    • Write SOPs, protocols, reports, and risk assessments
    • Ensure compliance with cGMP and regulatory requirements

    Support audits and inspections



    Sourced from naukri

    Skills

    pharmaceuticsFormulationLife Sciences

    About BDR Pharmaceuticals International

    BDR Pharmaceuticals International logo

    BDR Pharmaceuticals International

    Pharma

    2.5k+

    employees

    2002

    24 years old

    Mumbai, Maharashtra

    US

    ₹4.5L PA avg

    Avg at BDR Pharmaceuticals International

    About

    BDR Pharmaceuticals International comprising of API and formulation manufacturing, focuses on development in 4 specialized therapeutic segments such as Oncology, Critical care, Gynecology & Neurology.

    Industries

    Pharma

    Employee ratings

    10 reviews

    4.1/ 5

    Culture

    4.7

    Career growth

    3.9

    Work-life

    4.0

    Employees rate it well for

    Job Security42Company Culture41

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    Walk-in || ADL - Officer / Executive · waiting for your command