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Regulatory Affairs Associate – Corteva Agriscience

Published on

Corteva Agriscience

Bachelor’s degree in Information, Chemistry, Biology, or a related scientific discipline

Hyderabad

1 - 3 Years

Verified Job

Online Application
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Are you passionate about compliance, documentation, and global regulatory processes? A leading pharmaceutical company is hiring a Regulatory Affairs Associate in Hyderabad, Telangana, India. This site-dedicated role is a contract position (through a third-party vendor) and offers a chance to work in global operations, regulatory submissions, and cross-functional collaboration.

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This position is ideal for candidates with a scientific background and a keen eye for detail who are looking to build their career in pharmaceutical regulatory affairs.


Key Responsibilities

As a Regulatory Affairs Associate, you will:

  • Coordinate preparation and delivery of global regulatory documents.
  • Collaborate with Country Regulatory Managers (CRMs), global regulatory teams, and manufacturing units.
  • Understand and implement local regulatory requirements.
  • Manage project timelines, prioritization, and reporting using tracking tools.
  • Archive documentation for compliance and traceability.
  • Monitor requests to ensure timely processing and business alignment.
  • Communicate project status updates to stakeholders.
  • Proactively interact with SMEs, regulatory staff, and operations for document-specific requirements.
  • Handle shifting priorities independently with strong organizational skills.
  • Drive continuous process improvements within the team.
  • Lead or support process improvement projects as needed.

Required Qualifications

  • Bachelor’s degree in Information, Chemistry, Biology, or a related scientific discipline (or equivalent experience).
  • Proficiency in MS Excel, Word, PowerPoint, SharePoint, and database tools.
  • Strong organizational, project management, and communication skills.
  • Previous regulatory or technical experience preferred.
  • Experience in SAP EHS module is mandatory.

Benefits of Joining

  • Opportunity to work on global regulatory submissions.
  • Gain experience in a centralized regulatory operations environment.
  • Collaborate with cross-functional teams across technical disciplines.
  • Exposure to process improvements and project management in pharma operations.
  • Competitive compensation package.

Application Process

Application Link

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PharmaBharat Editorial Team

The PharmaBharat Editorial Team, comprised of pharmaceutical industry experts with over 3 years of collective experience in research, regulatory affairs, and market analysis, delivers accurate and timely updates on trends, innovations, and career opportunities. Our content is rigorously vetted by professionals with advanced degrees in pharmacy and biotechnology, ensuring authoritative and trustworthy insights for job seekers in the pharmaceutical sector.

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