GMP Process Engineer – CQV for Biopharma (Toronto)

Integra People Ltd; Halifax; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading engineering organization in Halifax, UK, is looking for a Process Engineer to design GMP-compliant integrated process equipment for the pharmaceutical industry. The successful candidate will collaborate in all project phases and must be willing to live in Toronto, Canada, for the first 12 months. This role offers a dynamic work environment with opportunities for international assignments.

Qualifications

• 3-5 years of relevant experience within the pharmaceutical or biopharmaceutical industry preferred.

Responsibilities

• Developing design bases and evaluating process alternatives.
• Preparing User Requirement Specifications (URS).
• Creating Process Flow Diagrams (PFDs) and Piping & Instrumentation Diagrams (P&IDs).
• Integrating process unit operations and designing equipment layouts.
• Sizing and specifying process equipment.
• Supporting commissioning and qualification protocol development and execution.

Skills

Strong interpersonal and teamwork skills

Excellent organizational and time-management abilities

Strong written and verbal communication skills

Education

Bachelor's degree in Engineering (Chemical, Mechanical, or related discipline)

Job description

A leading engineering organization in Halifax, UK, is looking for a Process Engineer to design GMP-compliant integrated process equipment for the pharmaceutical industry. The successful candidate will collaborate in all project phases and must be willing to live in Toronto, Canada, for the first 12 months. This role offers a dynamic work environment with opportunities for international assignments.