Senior Regulatory Affairs Coordinator

2 days ago


Chennai, Tamil Nadu, India beBeeCompliance Full time ₹ 30,00,000 - ₹ 75,00,000
Job Description:
We are seeking a diligent Legal Compliance Specialist to join our organization. In this role, you will be responsible for reviewing and drafting agreements, as well as maintaining accurate records related to the legal structure of US entities. This position requires a strong understanding of contractual concepts and ability to perform routine administrative tasks.

Responsibilities:
  • Review and draft agreements, including other related documents such as board consents.
  • Maintain accurate records related to the legal and operational structure of US entities, ensuring compliance with internal policies and US corporate law.
  • Understand basic contractual concepts such as indemnification and limits of liability.
  • Perform routine administrative tasks including uploading files, communicating with internal and external clients, maintaining log notes, photocopying, faxing, and scanning documents.
  • Provide executive administrative support, handling confidential correspondence with a high degree of discretion and initiative.
  • Ability to handle multiple processes concurrently.
  • Manage legal invoices and ensure timely payment.
  • Complete necessary forms ensuring entities are properly qualified in the US.
  • Assist with project management tasks, ensuring accuracy and timely completion of assignments.
  • Conduct special projects as assigned.
  • Proactively address customer issues related to support requirements.

Requirements:
  • Total work experience: 1-3 years.
  • Educational qualification: Associate degree in Law or a minimum of two years' related experience, or an equivalent combination of education and experience. Strong logical reasoning and analytical skills are a must.
  • A passion for continuous learning and professional growth.
  • Excellent communication skills (both oral and written).
  • Strong computer skills, with proficiency in MS Office applications (especially Excel, Word, PowerPoint, and SharePoint).
  • High attention to detail.
  • Ability to work independently as well as in a team. Must be self-motivated, adaptable, and possess a positive attitude.
  • Capability to manage multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
  • Strong proficiency in Microsoft Office, including advanced Excel, PowerPoint, and Internet research.
  • Understanding of and commitment to maintaining client confidentiality.
  • Ability to adapt to changes in the work environment, manage competing demands and deadlines, and handle frequent changes, delays, or unexpected events.
  • Strong critical thinking skills, using logic and reasoning to evaluate alternatives, conclusions, and problem-solving approaches.

  • Regulatory Affairs

    3 weeks ago


    Chennai, Tamil Nadu, India Ababil Healthcare Full time

    Role - Regulatory Affairs - Medical Devices Experience - 1 to 3 Years Location- Madhavaram Chennai Budget - As per the industry Key Responsibilities 1 Regulatory Submissions Prepare and submit regulatory documents to authorities for approval such as new product applications amendments and supplements 2 Compliance Ensure products meet...


  • Chennai, Tamil Nadu, India beBeeRegulatory Full time ₹ 15,00,000 - ₹ 25,00,000

    Regulatory Affairs Specialist Job OpportunityThe ideal candidate for this position will have a strong background in regulatory affairs, with a focus on CMC and USFDA submissions.A key responsibility of the role is leading and managing CMC regulatory activities, including preparing and reviewing technical documents such as Module 2 & 3 (CTD format).Key...


  • Chennai, Tamil Nadu, India beBeeRegulatory Full time ₹ 90,00,000 - ₹ 1,20,00,000

    Regulatory Submission Expert Job Description: As a Regulatory Affairs professional, you will play a crucial role in ensuring the successful submission of regulatory documents for pharmaceutical products. This includes preparing and reviewing new ANDA filings, amendments, and Annual reports to the ANDA. Key Responsibilities: 1. Prepare and review regulatory...


  • Chennai, Tamil Nadu, India Seven Consultancy Full time

    JOB DETAILS Candidates should review and prepare regulatory submissions, including new ANDA filings, amendments and Annual reports to the ANDA.Review of DMF Manages USFDA registration activities FUNCTIONAL AREA Pharma Jobs Consultancy in Chennai, Pharma Jobs Consultancy near me, Pharma Jobs, Top, Best, Jobs Consultancy in Chennai, regulatory affairs jobs...


  • Chennai, Tamil Nadu, India Thepharmadaily Full time

    Job Description- Prepare, review, and submit amendments and supplements for the assigned products.- Prepare summary documents for regulatory submission.- Prepare, review, and submit responses to the Agency s queries for the assigned products.- Compile and submit Global Annual Reports.- Review stability protocols and reports, analytical method validation...


  • Chennai, Tamil Nadu, India Buckman Full time

    Job DescriptionDescriptionRegulator ChemistLocation: Chennai, IndiaRequired Language: EnglishEmployment Type: Full-TimeSeniority Level: AssociateTravel Mode: ModerateAbout UsBuckman is a privately held, global specialty chemical company with headquarters in Memphis, TN, USA, committed to safeguarding the environment, maintaining safety in the workplace, and...


  • Chennai, Tamil Nadu, India beBeeManagement Full time

    General Administrator RoleWe are seeking an experienced General Administrator to join our team. As a key member of the department, you will be responsible for overseeing projects, managing office facilities, and coordinating with vendors.Key Responsibilities:Project Management: Plan and oversee projects within the General Affairs department, developing...


  • Chennai, Tamil Nadu, India beBeeScientific Full time ₹ 15,00,000 - ₹ 25,00,000

    Job Title:Senior Scientific Content EditorWe are seeking a highly skilled and experienced Senior Scientific Content Editor to review, edit, and ensure the quality and accuracy of medical and scientific documents. This role involves working closely with medical writers and subject matter experts to produce clear, consistent, and compliant content for...


  • Chennai, Tamil Nadu, India Icon Full time

    Medical Affairs Specialist - India Chennai Trivandrum - Office or Home BasedICON plc is a world-leading healthcare intelligence and clinical research organization Were proud to foster an inclusive environment driving innovation and excellence and we welcome you to join us on our mission to shape the future of clinical developmentOverview Provide support...


  • Chennai, Tamil Nadu, India beBeeCompliance Full time ₹ 1,00,00,000 - ₹ 2,00,00,000

    Job TitleSenior Business Analyst with HealthCareJob DescriptionGather, analyze and document business requirements related to regulatory compliance and payer guidelines. Ensure system changes, processes and documentation remain compliant with regulations.Key Responsibilities:Regulatory ComplianceBusiness Requirements AnalysisSystem Change...