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Graduate Intern – CMC RA, Delivery, Small Molecules Mature Products

  • Company: GSK
  • Location: India
  • Full Time
  • India
  • Apply on company site
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GSK at a glance

gsk.com
  • Founded 2000
  • Employees 97921
  • Ticker GSK
GSK 53.32 USD +0.97%

Investor research: Yahoo Finance · SEC filings

Source: Wikipedia

Join GSK as a Graduate Intern in Chemistry, Manufacturing, and Controls (CMC) Regulatory Affairs, based in India. This full-time internship offers hands-on experience in pharmaceutical regulatory documentation and the maintenance of small molecule products throughout their market lifecycle.

About This Position

As a CMC RA graduate intern, you'll work within GSK's Regulatory Affairs division supporting the Chemistry, Manufacturing, and Controls aspects of our established pharmaceutical portfolio. Under the guidance of experienced regulatory professionals, you'll contribute to the preparation and maintenance of regulatory submissions and post-approval documentation. This role is fundamental to ensuring compliance with evolving regulatory and scientific standards across global markets, with a particular focus on our small molecule mature products.

Your Responsibilities

  • Prepare and assist in authoring CMC technical regulatory documents for marketing authorisation applications and lifecycle submissions
  • Support regulatory submissions across multiple therapeutic areas and geographic markets
  • Participate in lifecycle activities and maintenance of already-registered products
  • Utilise digital regulatory platforms (including RIM systems and structured data management tools) to organise and execute regulatory workflows
  • Ensure accuracy and completeness of regulatory data throughout the documentation lifecycle
  • Collaborate with cross-functional teams including quality, manufacturing, and scientific affairs

What We're Looking For

  • Recent graduate or final-year student in pharmaceutical sciences, chemistry, chemical engineering, or a related discipline
  • Understanding of pharmaceutical manufacturing, quality control, and regulatory frameworks
  • Strong written communication skills and attention to detail in technical documentation
  • Ability to work effectively under supervision whilst managing multiple tasks
  • Familiarity with regulatory terminology and requirements in pharmaceuticals (advantageous)
  • Proficiency with Microsoft Office and learning aptitude for regulatory information management systems

More About GSK

GlaxoSmithKline (GSK) is a research-driven global pharmaceutical and biologics company committed to improving health and quality of life. Our operations span the discovery, development, manufacturing, and commercialisation of medicines and vaccines. In India, GSK maintains a significant presence supporting local patient needs and contributing to our global supply chain for innovative and established pharmaceutical products.

How to Apply

To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.

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India, officially the Republic of India, is a country in South Asia. It is the seventh-largest country by area, the most populous country in the world and, since its independence in 1947, the world's most populous democracy. Bounded by the Indian Ocean on the south, the Arabian Sea on the southwest, and the Bay of Bengal on the southeast, it shares land borders with Pakistan to the west; China, Nepal and Bhutan to the north; Bangladesh and Myanmar to the east. In the Indian Ocean, India is near Sri Lanka and the Maldives. Its Andaman and Nicobar Islands share a maritime border with Myanmar, Th

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    Graduate Intern – CMC RA, Delivery, Small Molecu… GSK
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