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RegRegulatory Executive Graduate Jobs in Pune

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  • 4 - 6 yrs
  • 5.0 Lac/Yr
  • Pune
Procurement Strategy Material Procurement Purchase Planning Purchase Orders Market Research Vendor Negotiation Cost Management Vendor Relationship Management Vendor Management Vendor Development Convincing Power Fire Safety Supplier Management Inventory Managment Budgeting Regulatory Compliance
Job Summary:We are seeking an experienced and skilled Fire Senior Purchase Engineer/Executive to join our team. The successful candidate will be responsible for managing the procurement of fire safety equipment, materials, and services for our organization. This includes sourcing, evaluating, and selecting suppliers, negotiating prices and terms, and ensuring that all purchases are made in accordance with company policies and procedures.Key Responsibilities:1. Procurement of Fire Safety Equipment and Materials:2. Supplier Management:3. Purchase Order Management:4. Inventory Management:5. Budgeting and Cost Control:6. Compliance and Regulatory:7. Communication and Collaboration:Must Have :Strong knowledge of procurement principles and practicesExcellent communication and negotiation skills- Ability to work independently and as part of a team- Strong analytical and problem-solving skillsIndustry Knowledge:- Strong knowledge of fire safety equipment, materials, and services
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Visa Executive

Ishwa Holidays Pvt Ltd

  • 1 - 2 yrs
  • 5.0 Lac/Yr
  • Pune
Continuous Improvement Application Submission Compliance and Regulatory Awareness Communication and Customer Service Record Keeping Visa Executive Walk in
Job Overview:As a Visa Executive, you will be responsible for managing and facilitating the visa application process for individuals or corporate clients. Your role involves ensuring compliance with immigration laws and regulations, providing guidance to applicants, and maintaining accurate records. Attention to detail, strong communication skills, and a thorough understanding of visa procedures are essential for success in this position.Key Responsibilities:Client Consultation:Conduct consultations with clients to understand their visa requirements and provide information on the necessary documentation.Advise clients on visa categories, eligibility criteria, and any changes in immigration policies.Document Verification and Preparation:Review and verify all visa application documents for accuracy and completeness.Prepare and organize visa applications according to specific country requirements.Collaborate with clients to collect additional information or documentation as needed.Application Submission:Submit visa applications to the relevant immigration authorities in a timely manner.Track the status of applications and provide regular updates to clients.Address any issues or discrepancies with submitted applications promptly.Compliance and Regulatory Awareness:Stay informed about changes in immigration laws, policies, and procedures.Ensure strict adherence to all relevant immigration regulations and compliance standards.Provide guidance to clients on potential challenges and mitigation strategies.Communication and Customer Service:Maintain clear and effective communication with clients throughout the visa application process.Respond to client inquiries promptly and professionally.Address and resolve any issues or concerns raised by clients.Record Keeping:Maintain accurate and up-to-date records of all visa applications and related documents.Generate reports on visa application statuses, approvals, and rejections.
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Drug Regulatory Affairs Executive

Viviora Lifesciences Pvt. Ltd.

  • 0 - 3 yrs
  • 3.0 Lac/Yr
  • Pune
Drug Regulatory Affairs Pharmacology Quality Assurance Formulations Regulatory Affairs Executive Work From Home
We have vacancy for 2 Drug regulatory affairs executive Jobs in Pune for Freshers Educational Qualification : B.Pharma, B.Sc, M.Pharma, M.Sc Skill Drug Regulatory Affairs,pharmacology,quality assurance,Formulations etc.
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  • 3 - 5 yrs
  • 3.5 Lac/Yr
  • Pune
Quality BMR BPR Pharma Regulatory Walk in
1. Manufacturing process validation, product development records, dossiers, BMR, BPR, stability data analysis etc.2. Food and Drug Administration (FDA) related work, Loan License Documentation, Certificate of Pharma Products (COPP) registrations, etc.3. Department coordination to manufacturing for QA / QC, R&D, Legal, etc.4. Preparing & reviewing art works, labels, pack inserts, etc.5. Response to various queries from various departments, etc.
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