Urgent: Drug And Excise Regulatory Affairs Executive

2 weeks ago

Panchkula HR IN Dr. Lormans Homeopathic Associates Pvt. Ltd. Full time

Job Title Drug and Excise Regulatory Affairs Executive Company Dr Lorman s Homeopathic Associates Pvt Ltd Location Panchkula Haryana Reports To Regulatory Affairs Manager Senior Management Job Summary Dr Lorman s Homeopathic Associates Pvt Ltd is seeking a dedicated Drug and Excise Regulatory Affairs Executive to manage regulatory compliance and excise matters for our homeopathic product line The role involves preparing and managing submissions to the FDA ensuring compliance with drug laws and handling all excise documentation and processes Key Responsibilities Prepare and submit product dossiers license applications renewals and variations to the FDA India with support of previous staff Ensure all products comply with the Drugs and Cosmetics Act and applicable homeopathic regulations Liaise directly with the FDA and other relevant government bodies for timely approvals renewals and issue resolution Stay updated on regulatory changes circulars and notifications affecting homeopathic products Review product packaging labeling and promotional material for compliance with FDA requirements Support FDA inspections and audits ensure all records and documents are audit-ready Maintain detailed regulatory trackers archives and filing systems for product and excise documentation Requirements Bachelor s or Master s degree in Pharmacy Chemistry Life Sciences or a related field 2-4 years of regulatory affairs experience preferably in homeopathic or pharmaceutical companies Good understanding of India s Drugs and Cosmetics Act and FDA regulatory requirements Strong knowledge of excise documentation and reporting Excellent organizational skills with attention to detail and accuracy Effective communication skills to liaise with regulatory bodies and internal teams Proficiency in MS Office Word Excel PowerPoint Preferred Skills Bonus Prior experience working specifically with homeopathic products or natural remedies Familiarity with FDA online portals and submission processes Experience managing regulatory audits and inspections What We Offer An opportunity to work with one of the trusted names in the homeopathic sector A supportive collaborative environment focused on quality and compliance Competitive salary and benefits Job Type Full-time Pay 20 000 00 - 26 000 00 per month Benefits Paid sick time Paid time off Schedule Day shift Weekend availability Supplemental Pay Overtime pay Yearly bonus Work Location In person

  • Executive Officer Drug Regulatory Affairs

    22 hours ago

    Panchkula, India Venus Remedies Full time

    Executive Officer Drug Regulatory Affairs (DRA) Job Posting: 10/11/2021 Panchkula JOB REQUIREMENTS Mandatory Qualifications Work Experience in Relevant Field 2.5-5 Years Technical Skills Required Who You'll Work With Regulatory Authorities What You'll Do Registration of new pharmaceutical drug Product.Renewal of approval of existing drug products....

  • Drug Regulatory Affairs Executive

    2 weeks ago

    Panchkula, Haryana, India Venus Remedies (VRL) Full time ₹ 15,00,000 - ₹ 25,00,000 per year

    Role & responsibilitiesJob Summary:We are looking for a skilled and motivated Senior Executive Drug Regulatory Affairs to support the registration and maintenance of injectable pharmaceutical products across ROW (Rest of the World) markets. The ideal candidate will have experience in compiling and submitting dossiers in accordance with country-specific...

  • Regulatory Affairs Executive

    2 weeks ago

    Sonipat, HR, IN Nextgen Group Services Full time

    Required Medical Devices Ltd Company Urgent Vacancy - Regulatory Affairs Executive Male Salary Upto - 4 80 LPA Qualification -B Tech ME Medical Science Skill Cross-Functional Collaboration Technical Writing Regulatory Guidance Experience -03 to 04 Years Medical Devices Equipment Job Location Sonipat Haryana Interested candidates can contact us at...

  • Regulatory Affairs Executive

    23 hours ago

    Panchkula, India cosmetify Full time

    **Job description** 1.Prepare and submit regulatory documents with Food and Drug Administration for product approvals and renewals 2. Maintain up-to-date knowledge of regulatory requirements, guidelines, and industry trends. 3. Maintaining BMR and BPR records 4. Checking and approving Products artwork 5. Support regulatory inspections and audits,...

  • Manager Drug Regulatory Affairs

    3 weeks ago

    Panchkula, India Venus Remedies (VRL) Full time

    Role & responsibilities Regulatory Strategy Development: Develop and implement regulatory strategies for the registration and market access of pharmaceutical products, particularly injectables, in ROW regions including Africa, CIS, LATAM, etc. Monitor and assess regulatory trends, changes in legislation, and health authority requirements in these regions....

  • Manager Drug Regulatory Affairs

    2 weeks ago

    Panchkula, Haryana, India Venus Remedies (VRL) Full time ₹ 5,00,000 - ₹ 15,00,000 per year

    Role & responsibilitiesRegulatory Strategy Development:Develop and implement regulatory strategies for the registration and market access of pharmaceutical products, particularly injectables, in ROW regions including Africa, CIS, LATAM, etc.Monitor and assess regulatory trends, changes in legislation, and health authority requirements in these...

  • Drug Regulatory Affairs

    3 weeks ago

    Kathua, JK, IN Sanctus Global Formulations Ltd. Full time

    Ensuring Compliance Guaranteeing that drug development manufacturing and marketing align with national and international regulatory guidelines and industry standards Regulatory Submissions Preparing reviewing and submitting comprehensive dossiers and applications e g New Drug Applications NDAs Investigational New Drugs INDs to regulatory...

  • Assistant Manager Regulatory Affairs

    6 days ago

    Other City(s) in Maharashtra S Global Tech Full time ₹ 14,40,000 per year

    Job Description Urgent opening for a Pharmaceutical company Position: Regulatory AffairsExperience: 9-10 year exp (certification in RA, Registration, ACTD, ANDA, CTD module, Clinical Trial, Regulatory Submission, Global Regulatory Strategy)Education: B.Pharm/M.PharmSalary: 10 to 12 lpa Location: 1 Year working in Daman after 1 year will be relocated to...

  • Regulatory Affairs Executive

    1 week ago

    Panchkula, India jak pro solutions Full time

    **Key Responsibilities**: Prepare and compile documents for FDA approval, COA, MSDS and other regulatory submissions in line with updated industry standards and guidelines. Prepare, update, and maintain Batch Processing Reports (BPRs) as per regulatory and internal quality protocols. Verify product labels, packaging, and design for conformity with Legal...

  • Regulatory Affairs Officer

    1 week ago

    Panchkula, India TalentXplore Full time

    Assist in the preparation and review of regulatory dossiers in CTD/eCTD format for submission. - Support in the compilation of documentation for New Marketing Authorizations, Post-Approval Variations, and Renewals. - Coordinate with departments such as QA, QC, Production, R&D, and Packaging for data collation and timely submission. - Review and verify...