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    Job · 15140947

    Grifols logo

    Regulatory and Quality Specialist

    Grifols · Gurugram · onsite · Posted 52d ago

    Undisclosed2–10 yrsfulltimeSourced fromNaukri

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

    About this role

    Job Summary

    The focus of the Regulatory and Quality Specialist is to lead Regulatory Affairs activities for India and neighboring markets, ensuring the successful registration, approval, maintenance and lifecycle management of Grifols portfolio. In addition, the role supports local Quality Assurance and Pharmacovigilance activities, ensuring compliance with applicable regulations and company standards.

    Job Details

    • Location: Gurgaon, IN
    • Contract Type: Regular Full-Time
    • Area: Quality

    Responsibilities

    • Responsible for Regulatory Affairs activities in India and neighbouring markets, encompassing product registrations, regulatory submissions, approvals, renewals, lifecycle management, regulatory intelligence, and liaison with Health Authorities.
    • Develop and execute regulatory strategies aligned with business objectives, supporting product launches, portfolio maintenance, pricing activities and tender participation.
    • Ensure compliance with local Quality Management System (QMS) requirements, supporting audits, supplier qualifications, GDP activities and quality oversight of Third-Party Logistics providers.
    • Support Pharmacovigilance activities as local backup contact, ensuring compliance with local and global PV requirements, safety reporting and maintenance of PV procedures.
    • Collaborate closely with Commercial, Medical Affairs, Supply Chain, Finance and Global teams to support business growth while maintaining full regulatory and quality compliance.

    Who you are

    The requirements listed below are representative of the knowledge, skills, education and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

    • Degree in Pharmacy, Life Sciences or a related scientific discipline.
    • Experience in Regulatory Affairs within the pharmaceutical, biotechnology, medical device or healthcare industry.
    • Knowledge of regulatory submissions, approvals and interactions with health authorities, preferably in India and SAARC countries.
    • Strong stakeholder management, communication and organizational skills.
    • Ability to work effectively in cross-functional and multicultural environments.
    • Experience with regulatory and quality management tools such as Veeva, SAP, TrackWise or similar systems is considered a plus.
    • Fluent Hindi and English.


    Disclaimer: This job posting 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

    Skills

    SAPpharmacovigilancemedical affairsRegulatory AffairsPharmacyHealthcareSupply ChainStakeholder ManagementPharmaLife Sciences

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