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    Job · 18064908

    Aurigene Pharmaceutical Services logo

    Team Member- DQA

    Aurigene Pharmaceutical Services · Hyderabad · onsite · Posted 36d ago

    Undisclosed4–8 yrsfulltimeSourced fromNaukri

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

    About this role

    Roles and Responsibilities

    • Conduct analytical testing, stability studies, and method validation for API samples using various instruments such as HPLC, GC, UV spectrophotometer, etc.
    • Prepare protocols and SOPs related to QbD activities including Change Control Management.
    • Ensure compliance with regulatory requirements by reviewing documents like BPR's, SOP's, Method Transfer Protocols, Method Transfer Report, etc.
    • Collaborate with cross-functional teams to resolve issues related to documentation and review of documents.
    • Maintain accurate records of all experiments performed in the lab.

    Desired Candidate Profile

    • MS/M.Sc(Science) degree in Chemistry or equivalent qualification.
    • 4-8 years of experience in DQA team handling analytical methods development & validation.
    • Strong knowledge of ELN (Electronic Lab Notebook) Review process.
    • Experience with CDMO DQA operations is desirable.

    Sourced from naukri

    Skills

    Analytical& process developmentCDMO DQAELN (Electronic Lab Notebook) ReviewdoeqbdChange Control ManagementDocumentation ReviewDevelopment Quality Assurance

    About Aurigene Pharmaceutical Services

    Aurigene Pharmaceutical Services logo

    Aurigene Pharmaceutical Services

    Pharma

    467

    employees

    2020

    6 years old

    Bangalore, Karnataka

    India

    ₹7.9L PA avg

    Avg at Aurigene Pharmaceutical Services

    About

    Aurigene Pharmaceutical Services is a leading contract research, development and manufacturing organization(CDMO) providing end-to-end solutions to pharma companies worldwide

    Industries

    Pharma

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