Ingénieur en procédés pharmaceutiques
- Employment type
- Full-time · On-site
- Posted
- September 26, 2026
- Province
- Quebec (QC)
Hiring confidence: Sparse posting · 11/100
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 role is based in Quebec. LAPORTE 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 en procédés pharmaceutiques 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
- Engineering degree (chemical or pharmaceutical engineering preferred)
- Professional engineering background in pharmaceutical or biotech industry
- Knowledge of pharmaceutical manufacturing processes
- Understanding of GMP and regulatory requirements
- Strong technical communication skills
Fit check
Is this role right for you?
Top skills this posting asks for:
- Pharmaceutical process engineering
- Chemical engineering
- Process design
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What you'll do
- Design and optimize pharmaceutical manufacturing processes
- Provide engineering consulting services to pharmaceutical clients
- Develop technical documentation and process specifications
- Support equipment selection and process validation
- Collaborate with cross-functional teams on engineering projects
- Ensure compliance with pharmaceutical regulations and standards
- Contribute to process improvement initiatives
What you'll need
- Engineering degree (chemical or pharmaceutical engineering preferred)
- Professional engineering background in pharmaceutical or biotech industry
- Knowledge of pharmaceutical manufacturing processes
- Understanding of GMP and regulatory requirements
- Strong technical communication skills
- Fluency in French and English