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    Pharmacovigilance Job at Macleods | Aggregate Report Reviewer | Pharma Graduates Eligible

    Macleods Announces Pharmacovigilance Job Opening | M Pharm Graduates Apply

    Looking for a Pharmacovigilance Job with one of India’s leading pharmaceutical companies? Macleods Careers brings an excellent opportunity for M.Pharm (Pharmacology) professionals to join as an Aggregate Report Reviewer – PBRER in the Pharmacovigilance Department at Andheri, Mumbai. If you have 1–2 years of experience in aggregate report review, this Pharmacovigilance Job under Macleods Careers could be your next career move.

    • Job Opening: Aggregate Report Reviewer – PBRER
    • Department: Pharmacovigilance
    • Location: Mumbai, Maharashtra

    About the Company

    Macleods Pharmaceuticals Ltd. is one of India’s leading pharmaceutical companies with a strong presence in research, development, manufacturing, and global healthcare markets. Macleods Careers offers exciting opportunities for professionals seeking growth in pharmacovigilance, regulatory affairs, quality, research, and manufacturing.

    Job Description

    Macleods Pharmaceuticals is inviting applications for the position of Aggregate Report Reviewer – PBRER. This Pharmacovigilance Job involves reviewing aggregate safety reports, coordinating submissions, preparing compliance documentation, and ensuring adherence to global pharmacovigilance guidelines under Macleods Careers.

    Key Responsibilities

    • Quality review of PSUR, PBRER, and ACO, RMP (Europe/UK, India, ROW countries).
    • Preparation of PSUR/PBRER/ACO calendar and allocation to the team.
    • Tracking of all reports to ensure that they are submitted on time to the RA/LRP or other respective authority.
    • Preparing and Training of SOP and SGD as per the guideline requirements.
    • Handling queries from agencies/authorities and preparing responses to queries.

    Qualification

    • Education: M. Pharma (Pharmacology)
    • Experience: 01 to 02 years of experience in the review of aggregate reports.
    • Technical Skills Required: Microsoft Office, Word, and PowerPoint.

    Contact Information

    Why Join This Role?

    • Join one of India’s leading pharmaceutical companies with a strong global presence.
    • Build your expertise in aggregate safety report review, including PSUR, PBRER, ACO, and RMP.
    • Gain exposure to international pharmacovigilance regulations covering Europe, the UK, India, and ROW countries.
    • Work with an experienced Pharmacovigilance team in a collaborative and professional environment.
    • Enhance your knowledge of global drug safety reporting, compliance, and regulatory documentation.

    CLICK HERE FOR ORIGINAL NOTIFICATION

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