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Technology Transfer - Executive

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Onsite

Technology Transfer - Executive

Encube Ethicals

Technology Transfer - Executive

Skills

Testing & QACompliance

25 days ago

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Important information


Contract type:

Permanent

Location:

Dhar, Madhya Pradesh 454001, India

Work mode:

Onsite

Published on:

1 October 2026

What they need


We're Hiring | Executive - Technology Transfer

Location: Indore, Madhya Pradesh

Company: Encube Ethicals Limited

Join Encube Ethicals, a global leader in topical pharmaceutical formulations, and be part of our Technology Transfer team, supporting Derma/Topical product technology transfer, PDL/MS&T activities, and manufacturing execution.

Key Responsibilities

  • Coordinate Technology Transfer activities for Derma/Topical dosage forms in collaboration with PDL, MS&T, Manufacturing, QA, QC, and other CFTs.
  • Support technology-transfer documentation, process GAP assessment, and technical discussions for new and transferred products.
  • Monitor submission/engineering batches during execution and ensure timely resolution of technical and documentation-related issues.
  • Support PDL/MS&T activities related to process understanding, scale-up, process transfer, and manufacturing execution.
  • Initiate and coordinate Change Controls and support preparation/review of Batch Records and validation/verification protocols.
  • Support Process Risk Assessment and stability protocol review for transferred products.
  • Ensure compliance with GMP, GDP, and QMS requirements throughout technology-transfer activities.
  • Support introduction of new process technologies and ensure projects are executed within defined timelines.

Desired Candidate Profile -

  • B. Pharma / M. Pharma.
  • 4-7 years of experience in Derma/Topical Manufacturing, Technology Transfer, PDL, or MS&T.
  • Strong understanding of topical/dermatological dosage forms and manufacturing processes.
  • Working knowledge of Technology Transfer and PDL/MS&T documentation and activities.
  • Knowledge of GMP, GDP, Change Control, Batch Records, Process Validation/Verification, and Risk Assessment.
  • Exposure to stability studies and ICH stability conditions.
  • Experience with US/EU regulatory markets will be an advantage.
  • Strong technical documentation, coordination, and cross-functional communication skills.

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