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Open nowPosted 4 hours agoWe saw it 117 min after it went up

Regulatory Affairs Senior Associate (Pre - Approval) - DEMO Global Services

Demo S.A.

Where
Hyderabad, TS, India
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Your applicationOpen nowRegulatory Affairs Senior Associate (Pre - Approval) - DEMO Global ServicesDemo S.A. · Hyderabad, TS, India

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  6. 58.9%60 days
This job: posted 4 hours ago

The posting

The Regulatory Affairs Senior Associate will work at the interface of R&D and Regulatory, building a genuine technical understanding of the product's formulation and analytical profile to support sound regulatory strategy. This is not a document-processing role — it requires the ability to engage with development science, identify potential issues, and contribute informed regulatory thinking rather than just administrative submission support.

Responsibilities

  • Develop a working technical understanding of assigned products — formulation composition and rationale, manufacturing process, and analytical/impurity profile — sufficient to identify regulatory implications independently.
  • Review R&D and Analytical data, including formulation trials, stability studies, method validation and characterization data, critically to spot gaps, inconsistencies or risks.
  • Support the Manager/Director in framing regulatory strategy by contributing well-reasoned technical inputs.
  • Assess the regulatory impact of significant development changes and ensure that comparability, bridging or additional evidence requirements are addressed prospectively.
  • Prepare and/or review assigned dossier sections, briefing packages and responses to major authority questions, ensuring completeness.
  • Drive submission readiness, including gap closure, review cycles, issue escalation and completion against agreed milestones.

Requirements

Experience and Qualifications

  • Minimum 4 years of relevant pharmaceutical or biopharmaceutical industry experience.
  • Minimum 2–3 years of genuine exposure in R&D, either formulation development and/or analytical sciences.

Required Skills

  • Understanding of and hands-on experience with regulatory dossier structure and requirements, including CTD/eCTD, is preferred, though the primary emphasis of this role is technical/scientific understanding over document compilation.
  • Strong analytical thinking and the confidence to raise technical concerns proactively.
  • Clear written and verbal communication skills for cross-functional technical discussions.
  • Ability to manage multiple deliverables independently within defined timelines.

Added Advantage

  • Experience with complex injectables, biologics/biosimilars, drug-device combination products or other technically complex dosage forms.

Benefits

The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.

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