JU

Ingénieur(e) de procédés II / Process Engineer II

Montréal, Québec
On-site
Full-time
No salary posted3 days ago
Employment type
Full-time · On-site
Posted
November 10, 2026
Province
Quebec (QC)

Hiring confidence: Sparse posting · 22/100

This posting is missing most of the signals we look for, or shows patterns common to listings that are not actively being filled. Check with the employer before applying. How this is scored

Job Overview

This is only part of this posting — the job board it came from publishes a short summary. Read the full posting.
Rejoignez un leader de la fabrication pharmaceutique — et participez à l'avenir Jubilant HollisterStier LLC est un leader bien établi dans les secteurs pharmaceutique et biopharmaceutique, offrant une gamme complète de services de fabrication qui contribuent à la mise au point de médicaments qui changent des vies partout dans le monde. Nous sommes reconnus à l'échelle nationale pour notre expertise dans la production de flacons stériles pour injection et de produits lyophilisés, et notre divisi…

This role is based in Quebec. Jubilant Pharma Limited is hiring for this full-time position through Jobily, where you can check how well your resume matches the posting before you apply.

Market context

About this role in Quebec

Average salary for Ingénieur(e) de procédés II / Process Engineer II in Quebec

We do not have a salary benchmark for this title in Quebec yet. The posting does not state a salary either.

NOC code

This posting has not been matched to a NOC 2021 unit group yet. Use the NOC finder to identify the code from the duties listed above.

Typical qualifications for Canadian employers

  • Bachelor's degree in Chemical Engineering, Pharmaceutical Sciences, or related field
  • 2-5 years of pharmaceutical manufacturing experience
  • Knowledge of GMP and FDA regulations
  • Experience with sterile injectable or lyophilized product manufacturing
  • Strong technical and analytical skills

Fit check

Is this role right for you?

Top skills this posting asks for:

  • Process Engineering
  • Pharmaceutical Manufacturing
  • Quality Assurance

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What you'll do

  • Support development and optimization of manufacturing processes
  • Ensure compliance with regulatory requirements and company standards
  • Collaborate with cross-functional teams on process improvements
  • Document and validate process changes
  • Troubleshoot manufacturing issues
  • Contribute to technology transfer and scale-up activities
  • Support sterile injectable and lyophilized product production

What you'll need

  • Bachelor's degree in Chemical Engineering, Pharmaceutical Sciences, or related field
  • 2-5 years of pharmaceutical manufacturing experience
  • Knowledge of GMP and FDA regulations
  • Experience with sterile injectable or lyophilized product manufacturing
  • Strong technical and analytical skills
  • Ability to work in a regulated environment

About the Company

JU

Jubilant Pharma Limited