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    Job · 15681009

    Aarti Pharmalabs logo

    Senior Executive -Global Regulatory Deficiency Centre

    Aarti Pharmalabs · Mumbai · onsite · Posted 48d ago

    Undisclosed6–8 yrsfulltimeSourced fromNaukri

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

    About this role

    Role & responsibilities

    Key Responsibilities:

    API Process Development & Optimization:

    • Perform feasibility studies, process optimization, and scale-up of API processes. Conduct process verification and identify Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs).
    • Plan lab work, prepare Reference Standards (RS)/Working Standards (WS), and ensure their characterization.
    • Initiate the technology transfer process to the pilot plant or production facility.

    Regulatory Affairs & Compliance Support:

    • Provide timely technical support for regulatory queries, especially those related to DMF preparation.
    • Ensure accurate preparation of specification sheets and MSDS for raw materials and intermediates.
    • Prepare the Development History Report for regulatory submission and archival. Conduct initial stability studies for developed products.

    Cross-Functional Coordination:

    • Coordinate with the Regulatory Affairs (RA), Analytical Development Lab (ADL), IPR, and Development Quality Assurance (DQA) teams.
    • Manage coordination between officers working in R&D.

    Required Qualifications & Experience:

    • Education: M.Sc. (Organic Chemistry) or Ph.D. (Organic Chemistry) Experience: 2 to 8 years of relevant experience


    Sourced from naukri

    Skills

    Regulatory AffairsAdlC plus plusDevelopment Quality Assurance

    About Aarti Pharmalabs

    Aarti Pharmalabs logo

    Aarti Pharmalabs

    Pharma

    2.0k+

    employees

    Mumbai

    India

    ₹6.6L PA avg

    Avg at Aarti Pharmalabs

    About

    Aarti Pharmalabs Limited (APL) is a leading Indian manufacturer of Pharmaceuticals and Nutraceuticals with a global footprint. We deliver process chemistry expertise, with a scale-up engineering competence, regulatory support and long-term supply by maintaining quality and timely delivery to create a sustainable future.

    Over the last two decades, APL serving global clients with top notch scientific knowledge, industry experts, state-of-the-art R&D and USFDA, EUGMP, EDQM, KFDA inspected manufacturing facilities. We manufacture Generic APIs, Intermediates and Xanthine derivatives. We offer CDMO services for small molecules drug substances (API/NCE/RSM/Intermediate) process development and manufacturing focusing on Ph-I/II/III, launch and commercial phase projects for Innovator Pharmaceutical and Biotech companies. We have been helping our clients to bring their molecules to market quickly and efficiently from clinical development through commercial stage manufacturing.

    We have dedicated facilities to manufacture HPAPIs, Corticosteroids, Cytotoxic and Oncology products.

    We are one of the preferred partner for Beverages and Nutraceuticals Industries for our flagship product ‘Caffeine’.

    Industries

    Pharma

    Employee ratings

    10 reviews

    3.6/ 5

    Culture

    2.6

    Career growth

    2.1

    Work-life

    3.1

    Employees rate it well for

    Job Security39Overall Company36

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