Regulatory Affairs Associate

6 months ago


Hyderabad Telangana, India Dr Reddy's Laboratories Limited Full time

CTD Dossier Drafting (Modules 2, 3, 4)
- Regulatory writing
- Clinical Regulatory & Pharmacovigilance Regulatory
- Regulatory commitment & compliance
- Any other Regulatory activities on need basis
- Support Line manager & Matrix manager in Regulatory projects
- Coordination and interaction with cross-functional teams

Mandatory Skills

Effective Regulatory/dossier writing skills; Effective interpersonal & communication skills; Good Analytical, reasoning, scientific & Regulatory aptitude; Positive attitude & behaviour
**Qualifications**
M.Sc / M.pharm



  • Hyderabad, India Parexel Full time

    Hyderabad, India **Job ID** R0000012328 **Category** Regulatory / Consulting **ABOUT THIS ROLE**: **Regulatory Affairs Associate** Must have experience in Regulatory Affairs-CMC, should be willing to work in EU Shifts. - To provide regulatory input on procedural and CMC documentation requirements specific to as defined by Health Authorities for assigned...


  • hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory Affairs Reports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...


  • hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...


  • hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, India POSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements. KEY...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory Affairs Reports To: Director, Regulatory Affairs Location: Hyderabad, Telangana, India POSITION DESCRIPTION The RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory...


  • hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, India POSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements. KEY...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, India POSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements. KEY...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title:Associate, Regulatory AffairsReports To:Director, Regulatory AffairsLocation:Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...


  • Hyderabad, India SteriMax Inc. Full time

    Position Title: Associate, Regulatory AffairsReports To: Director, Regulatory AffairsLocation: Hyderabad, Telangana, IndiaPOSITION DESCRIPTIONThe RA Associate will prepare regulatory submissions for generic drug products and actively participate in the management of submissions under regulatory agency review to fulfill Canadian regulatory requirements.KEY...

  • R&d Regulatory Affairs

    3 months ago


    Hyderabad, Telangana, India PepsiCo Full time

    Overview: - This role involves supporting the Regulatory Affairs team by serving as a Discipline Approver, ensuring compliance with regulatory standards for raw material specifications. Located within the Mexico Business Services or Hyderabad Business Services, you will play a key part in maintaining adherence to regulations within the designated business...


  • Hyderabad, India Medtronic Full time

    Careers that Change Lives Collaborate and partner with Design QA, R&D, Sustaining Engineering, Clinical Affairs, Marketing and Operations.Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.Responsible for supporting the needs of the MEIC with regulatory support for research and...


  • Hyderabad, Telangana, India IQ-EQ Full time

    **Company Description** IQ-EQ is a leading Investor Services group which combines global expertise with an unwavering focus on client service delivery. We support fund managers, global companies, family offices and private clients operating worldwide. IQEQ is a preeminent service provider to the alternative asset industry. IQEQ works with managers in...


  • Hyderabad, India TeizoSoft Private Limited Full time

    About the job:- A Day in the Life Collaborate and partner with Design QA, RD, Sustaining Engineering, Clinical Affairs and Operations.- Supports the Global Operating Unit Regulatory Affairs function as the local representative for ensuring requirements are met.- Responsible for supporting the needs of the regulatory support for research and development...


  • Hyderabad, Telangana, India Lifelancer Full time

    About the RoleAs a Senior Regulatory Affairs Specialist at Medtronic, you will play a crucial role in ensuring compliance with regulatory requirements and ensuring the success of our products in the global market. This is an exciting opportunity for a talented professional to join our team and make a significant impact.Key ResponsibilitiesPrepare, review,...


  • Hyderabad, India Parexel Full time

    When our values align, there's no limit to what we can achieve.   Senior Regulatory Affairs Associate Around 4-8 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologics) in various markets. Good understanding of regulatory framework, including regional trends,...


  • Hyderabad, Telangana, India Medtronic Full time

    At Medtronic, we're shaping the future of healthcare through innovative medical technology. As a Regulatory Affairs Specialist, you'll play a critical role in ensuring our products meet regulatory requirements and exceed customer expectations. Job OverviewWe're seeking an experienced Regulatory Affairs Specialist to join our team. In this role, you'll be...