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Reg Affairs Associate; Documentation

icon building Company : Sandoz
icon briefcase Job Type : Full Time

Number of Applicants

 : 

000+

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Job Description - Reg Affairs Associate; Documentation

Job Description Summary

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!

Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify & maintain records. Interprets and enforces all documentation formatting, standards, policies, and operating procedure requirements. May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers. May analyze and evaluate data, extract pertinent information, prepare information abstracts and executive summaries of material searched. May maintain extensive knowledge of product information andcontinuous contacts with local, regional, and unit customers.

Job Description

Your Key Responsibilities:

Your responsibilities include, but not limited to:

  • Learns to use basic principals, theories, and professional concepts.
  • Contacts are primarily with immediate supervisor and other personnel in department or group
  • Works on problems of routine scope.
  •  Follows established policies and procedures.
  • Normally receives detailed instructions on all work
  • Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt
  • Distribution of marketing samples (where applicable)

What you’ll bring to the role:

Essential Requirements:

  • Cross Cultural Experience.
  • 3+ years of relevant experience.
  • Collaborating across boundaries.
  • Operations Management and Execution.
     
  •  Skills:
  • Data Analysis.
  • Documentation Management.
  • Operational Excellence.
     

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported! 

Join us!

Skills Desired

Data Analysis, Documentation Management, Operational Excellence
Original job Reg Affairs Associate; Documentation posted on GrabJobs ©. To flag any issues with this job please use the Report Job button on GrabJobs.
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