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Research Associate

Himalaya Wellness Europe
Dubai, UAE
Full-time
Entry
Onsite
Discovered 1 weeks ago
Chemical engineeringManufacturing process developmentProcess scale-upTechnology transferManufacturing technologiesProcess validation

Full Job Posting

About the role

Process Engineer within Himalaya R&D, developing, optimizing, and industrializing manufacturing processes.

Translates R&D concepts into robust commercial processes while supporting quality, efficiency, scalability, and cost-effectiveness.

Works with R&D, manufacturing, quality, procurement, and regional supply teams across sites.

Key responsibilities

  • Assess manufacturing and packaging feasibility, equipment capability, machinery needs, and product-specific technical requirements at production sites.
  • Plan and lead laboratory, pilot, and industrial-scale trials for process development, scale-up, and technology transfer.
  • Support raw material procurement and qualification through technical trials, evaluations, and validation.
  • Design processes to improve quality, robustness, and scalability; reduce cost, energy use, processing time, and operational losses without compromising quality.
  • Set critical process parameters and quality requirements for consistent, reproducible product performance.
  • Coordinate technology transfer across sites and provide implementation, troubleshooting, and technical support to global manufacturing teams.
  • Assess process risks, establish mitigations, and transfer products from R&D through pilot scale into commercial production.
  • Support commercial validation and lead troubleshooting during scale-up and commercialization.
  • Prepare and maintain technical documentation, SOPs, process-transfer documents, trial reports, and quality records.

Experience and qualifications

  • B.Tech in chemical engineering.
  • One to five years of relevant industry experience is preferred.
  • Hands-on exposure to manufacturing technologies in FMCG, pharmaceutical, or dietary supplement industries.
  • Familiarity with US FDA requirements and global GMP practices is an advantage.
  • Prior exposure to scale-up trials, process development and validation, and technology transfer is preferred.
  • Good project coordination and project management capabilities.

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