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Design Process Engineer (JR)

PharmEng Technology

Toronto

On-site

CAD 60,000 - 80,000

Full time

4 days ago
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Job summary

A leading engineering firm in Toronto is seeking a Junior Design Process Engineer with 1-4 years experience in the Pharma industry. This role will involve delivering end-to-end solutions for integrated process equipment in GMP environments and requires collaboration with multi-functional teams. Candidates should be comfortable in a fast-paced environment and possess strong communication and leadership skills.

Qualifications

  • 1+ years in GMP process engineering, ideally with skidded systems.
  • Experience in process equipment and piping system design.
  • Commissioning & qualification experience (automated systems preferred).
  • Strong communication, organization, and leadership skills.

Responsibilities

  • Deliver end-to-end solutions for integrated process equipment.
  • Develop feasibility studies, mass balances, and utility sizing.
  • Guide projects from front-end engineering through start-up and CQV.
  • Collaborate with controls, validation, and QA teams.

Skills

GMP process engineering
Equipment and piping system design
Communication skills
Leadership skills

Tools

CAD
Process control systems

Job description

Design Process Engineer (Jr)
Location: Toronto, ON, CA
Industries: Biopharma
Full-Time | Engineering Design & CQV

We are looking for a Junior Design Process Engineer with 1- 4 years ofexperience in the Pharma industry. Pharma industry experience is a big plus.

What You'll Do:

As a Design Process Engineer,you'll be involved indelivering end-to-end solutions forintegrated process equipmentandunit operationsin GMP environments, from early design through CQV.

Key Responsibilities:
  • Conceptual, preliminary, and detailed process designs

  • Develop deliverables such as:

    • Feasibility studies, mass balances, utility sizing

    • Process simulations, PFDs, P&IDs, control strategies

    • URS, FDS, equipment specs, cost estimates

    • Bid packages, commissioning and qualification protocols

  • Guide projects from front-end engineering through start-up and CQV

  • Oversee equipment and utility design (e.g., fermenters, TFF, CIP systems)

  • Collaborate with controls, validation, and QA teams

  • Maintain strong relationships with multi-functional teams

What You Bring:
  • 1 + years in GMP process engineering, ideally with skidded systems

  • Experience in process equipment and piping system design

  • Commissioning & qualification experience (automated systems preferred)

  • Familiarity with CAD, process control, and validation coordination

  • Strong communication, organization, and leadership skills

  • Comfortable in a fast-paced, multi-project environment

This role offers true engineering creativity with exposure to a wide range of exciting, complex projects in a collaborative and technical environment.

#ProcessEngineering #PharmaJobs #Biotech #CQV #GMP #EngineeringCareers

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