Technical Expert Ms&t Bio Similar/ Large Molecules Ds/dp

Sandoz

Not specified; not specified; flexible working + l...
Hybrid
8-12 years biologics manufacturing experience
Upstream and downstream process design expertise
Knowledge of usfda ema ich regulatory guidelines
This role serves as the primary technical interface between Sandoz Bio Manufacturing sites and the Global MS&T Capability Hub for Large Molecule operations

Job Summary

  • This role serves as the primary technical interface between Sandoz Bio Manufacturing sites and the Global MS&T Capability Hub for Large Molecule operations.
  • The expert ensures robust process performance, product quality, and regulatory compliance across the entire product lifecycle while enabling efficient technology transfers.
  • Sandoz offers an agile and collegiate environment with impactful, flexible-hybrid careers where personal growth is encouraged.

Matching Summary

This role serves as the primary technical interface between Sandoz Bio Manufacturing sites and the Global MS&T Capability Hub for Large Molecule operations.

Salary

Not specified; Not specified; Flexible working and learning opportunities included

Skills & Requirements

Must-have

  • 8-12 years biologics manufacturing experience
  • Upstream and downstream process design expertise
  • Knowledge of USFDA EMA ICH regulatory guidelines
  • Experience with QbD DoE and statistical analysis
  • Process validation and cleaning validation skills

Nice-to-have

  • Strong cross-functional collaboration abilities
  • Experience in global matrix environment management
  • Ability to drive continuous improvement initiatives
  • Excellent communication and documentation skills

Key Requirements

  • Post Graduate degree in Pharmacy Biology or Bio tech
  • Ph.D. in Pharmaceutical Technology preferred
  • Fluency in English and regional languages required
  • Minimum 8-12 years relevant manufacturing experience

Work Rights

Not specified

Tailored Resume

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