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This job expired on 03/09/2026. It no longer accepts applications.

Process Specialist

Novartis

🇬🇧 English
process validation root cause analysis lean manufacturing

Job description

About the role

The Process Specialist provides front‑line technical and scientific support for all process‑specific issues, ensuring on‑time execution, compliance with cGMP, SOPs and relevant guidelines, and continuous improvement of quality and productivity.

Key responsibilities

  • Execute process validation activities and troubleshoot production processes.
  • Participate in root‑cause analysis, deviation handling and problem‑solving initiatives.
  • Coach personnel on Lean manufacturing principles and support line‑efficiency improvements.
  • Assist with product transfers, new introductions and review/approval of manufacturing documents.
  • Drive continuous‑improvement ideas to boost productivity within the process unit.
  • Implement day‑to‑day cGMP, HSE, DI and Novartis guideline compliance.

Required profile

  • Scientific degree (e.g., Pharmacy, Chemistry, Biology).
  • Previous experience in a pharmaceutical manufacturing environment.
  • Analytical and quality‑oriented mindset.
  • Fluent English communication skills.

Required skills

  • Process validation
  • Root cause analysis
  • Lean manufacturing
  • cGMP compliance
  • HSE compliance

What we offer

  • Opportunity to work for a global leader in healthcare.
  • Inclusive culture that supports diversity and disability inclusion.
  • Access to professional development resources and benefits.

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Published 2 months ago

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