Regulatory Affairs Officer

6 days ago


New Delhi, India A.P. Moller - Maersk Full time

A.P. Moller - Maersk is an integrated container logistics company working to connect and simplify its customers’ supply chains. As the global leader in shipping services, the company operates in 130 countries and employs roughly 76,000 people.With simple end-to-end offering of products and digital services, seamless customer engagement and a superior end-to-end delivery network, Maersk enables its customers to trade and grow by transporting goods anywhere - all over the world.Key Responsibilities:- Regulatory Compliance and Governance - Ensure the company fully complies with all applicable laws and regulations (SEZ FEMA, Income Tax Act, Companies Act, etc.). - Serve as the primary liaison with tax authorities, banks, auditors, and other regulators. - Business Operations Oversight - Oversee operations including documentation, asset management - Ensure accurate maintenance of records related to leased assets, lease counterparties, and financing. - Tax Compliance - Ensure timely filing of tax returns and other related compliances. - Internal Controls and Risk Management - Implement and monitor internal control frameworks for operational efficiency and risk mitigation. - Ensure adequate risk management mechanisms for credit risk, operational risk, and compliance risk. - Reporting & Disclosures - Ensure timely submission of required reports to authorities. - Supervise preparation and filing of audited financial statements. - Stakeholder Engagement - Manage relationships with banks, legal advisors, lessors, lessees, auditors, and regulatory authorities. - Strategic Advisory - Provide strategic guidance to management on regulatory changes, business development, and compliance matters.Qualification & Experience:- Chartered Accountant (CA), Company Secretary (CS), or equivalent professional qualification preferred. - Minimum 8-10 years of experience in compliance, finance, or regulatory functions (preferably in financial services or shipping). - Strong knowledge of SEZ regulations and Indian tax laws. - Excellent communication and analytical skills.



  • Delhi, India ProductLife Group Full time

    Responsibilities In the context of a project for one of our top Pharma client, we’re looking for 2 talented Regulatory Affairs Officer to lead the following missions, and much more!Compile, or supervise the compilation of regulatory dossiers Provide on-going regulatory advice to project teams to ensure regulatory concerns are planned and accounted for and...


  • Delhi, India NKG ADVISORY BUSINESS AND CONSULTING SERVICES PVT LTD Full time

    Regulatory Affairs Specialist - Legal Metrology and EPR India **Responsibilities**: Regulatory Compliance: Stay up-to-date with the latest Legal Metrology and EPR regulations in India. Ensure that all products and processes comply with these regulations. Documentation: Prepare and maintain all necessary documentation required for regulatory submissions,...


  • Delhi, India NKG ADVISORY BUSINESS AND CONSULTING SERVICES PVT LTD Full time

    **Job Title: Cosmetics Regulatory Affairs Specialist - Delhi** Key Responsibilities: - Conduct regulatory assessments of cosmetic products to ensure compliance with relevant regulations and guidelines - Prepare and submit regulatory dossiers to the appropriate authorities for import registration of cosmetics under COS 02 and COS 04 categories - Stay...


  • New Delhi, India Varex Imaging Corporation Full time

    Varex Imaging Regulatory Affairs Analyst participates in ensuring compliance of medical and industrial X-ray products. The Regulatory Affairs Analysts is a key player in a cross-functional team that includes Engineering, Manufacturing, Sales, Marketing, Quality and Customers. In addition, the regulatory affairs analyst is expected to perform the...


  • New Delhi, India Varex Imaging Corporation Full time

    Varex Imaging Regulatory Affairs Analyst participates in ensuring compliance of medical and industrial X-ray products. The Regulatory Affairs Analysts is a key player in a cross-functional team that includes Engineering, Manufacturing, Sales, Marketing, Quality and Customers. In addition, the regulatory affairs analyst is expected to perform the...


  • Delhi, Delhi, India Domnic Lewis Pvt. Ltd Full time

    **Executive - Regulatory Affairs - Delhi**: **Domnic Lewis has been mandated to hire for Executive - Regulatory Affairs - Delhi** **Position Title**: Executive - Regulatory Affairs **Grade**: C **Reports to**: Lead/Manager - Regulatory Affairs **Position Purpose**: - Monitor and report the status of all product licenses in a timely and accurate manner -...


  • New Delhi, India Ixoreal Biomed Full time

    About the Company : Shri Kartikeya Pharma is one of India’s leading nutraceutical companies, specializing in the manufacture of high-quality dietary supplement ingredients derived from root extracts.Title: Manager/Senior Manager- Global Regulatory Affairs Experience: 8–12+ yearsof Regulatory Affairs experience in Nutraceuticals, Dietary Supplements,...


  • New Delhi, India HCLTech Full time

    Experience: 2 to 5 yearsEducation: Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles in Quality Assurance, Regulatory Affairs, and Documentation in the Medical Devices domain.Skills & Requirements:Minimum 3 years of experience in Medical Devices Regulatory Affairs, Quality Assurance, or Documentation-...


  • New Delhi, India Gentell Full time

    Gentell is one of the largest vertically integrated wound care companies in the world. Based in Yardley, PA and with offices, distribution centers and manufacturing plants around the world, our purpose is to make a positive difference in the quality of life for the injured, the chronically ill and those near the end of life.Our success is a result of the...


  • New Delhi, India HCLTech Full time

    Experience:2 to 5 years Education:Bachelor's degree in Biomedical, Mechanical, or B.PharmWe are looking for talented professionals for roles inQuality Assurance ,Regulatory Affairs , andDocumentationin theMedical Devicesdomain.Skills & Requirements: Minimum 3 years of experience in Medical DevicesRegulatory Affairs ,Quality Assurance , orDocumentation Strong...