Skip to main content

Regulatory affairs

pharma courses

 

gpat

  • Walk In Drive for M.Pharm, B.Pharm, MSc in QC, Regulatory Affairs at Biological E. Limited

    Biochemical analysis such as protein content, sodium metabisulphite testing, HPLC, and sample management include receiving in-process samples, final bulk and final lot samples, distribution, and storage under appropriate storage conditions.
  • MSN Laboratories Hiring for API Regulatory Affairs Department
    Regulatory Submissions Prepare, submit, and manage regulatory filings for API products, including new drug applications, amendments, and variations, while ensuring compliance with relevant guidelines and regulations. API Equipment Handling.
  • Torrent Pharma Hiring M.Pharm, MSc Candidates in Regulatory Affairs Department
    Ensure the on-time filing of high-quality regulatory submission, and to assist in the preparation, maintenance, and control of regulatory dossiers. Interact with Regulatory agency on regulatory submissions and follow up for drug product approvals.
  • PAREXEL Hiring Regulatory Affairs Manager
    Experience in managing clinical trial studies, playing Regulatory Leads for Global trials, and exposure to the European market. Capitalizes on opportunities to improve project efficiency, results or team performance and proactively takes action. Leverages information from previous projects or other client work to efficiently complete assigned project activities as well as facilitate business decisions
  • Walk In Interviews for Formulation Regulatory Affairs at Hetero Drugs
    Candidates with experience in Formulation QA RA, Analytical, Formulation R&D, and interested in advancing their career in RA ROW, are encouraged to apply.
  • Work as Reg Affairs Officer at IQVIA
    Plans and coordinates activities to ensure regulatory lifecycle management activities and approvals are achieved by the Local Operating Company in a timely manner for all globally approved products.
  • Interview for M.Pharm in Regulatory Affairs at Sun Pharma
    Review of all the documents received from stake holder for dossier compilation , Query response and Life cycle management. Allocation of projects to regulatory associate & manage the team for all the regulatory submission activities
  • Work as Regulatory Affairs Associate Manager / Manager at Zydus Lifesciences
    To file amendments and deficiency response within timelines with go getter approach. The job requires review of documents related to DMF submission against predefined checklists and submission to various agencies globally.
  • Vacancy for M.Pharm, B.Pharm, M.Sc in Regulatory Affairs at JAMP group
    eCTD Compilation, validation, and submission to Health Canada and US through ESG gateway for New Submission ANDS, NDS, Deficiencies response Clarifax, SDN, NOD, NON, Supplements submissions
  • Thermo Fisher Scientific looking for Regulatory Affairs Manager

    Thermo Fisher Scientific Inc is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With revenues of 13 billion USD, we have approximately 39,000 employees and serve customers within pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions and government agencies, as well as in environmental and process control industries.

Subscribe to Regulatory affairs