Process Engineer

Integra People Ltd; Huddersfield; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading engineering organization is seeking a Process Engineer to join their team. The role involves relocating to Toronto, Canada for the first year. Candidates must have at least 12 months of experience in Pharma or Biotech process design. Job responsibilities include developing designs, preparing specifications, and supporting qualification processes. A Bachelor's degree in Engineering and 3-5 years of relevant experience are preferred. The position is primarily based in Halifax, UK and requires occasional international travel.

Benefits

Flights covered

Housing covered

Car provided

Fixed per diem for food and daily expenses

Qualifications

• 12 months experience in Pharma or Biotech Process Design required.
• 3-5 years of relevant experience in the pharmaceutical or biopharmaceutical industry preferred.

Responsibilities

• Develop design bases and evaluate process alternatives.
• Prepare User Requirement Specifications (URS).
• Create Process Flow Diagrams (PFDs) and Piping & Instrumentation Diagrams (P&IDs).
• Integrate process unit operations and design equipment layouts.
• Size and specify process equipment.
• Support commissioning and qualification protocol development and execution.

Skills

Strong interpersonal and teamwork skills

Ability to coordinate and support cross-functional project teams

Excellent organizational and time-management abilities

Self-motivated and capable of working independently

Strong written and verbal communication skills

Adaptable and effective in a fast-paced, multi-tasking environment

Education

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

Job description

Process Engineer

The successful candidate must be willing to live in Toronto Canada for the first 12 months.

AND

Have at least 12 months experience in Pharma or Biotech Process Design

All expenses covered;

• Flights
• Housing
• Car
• Fixed per diem (amount TBD) for food and miscellaneous daily incidentals

A leading engineering organization with international experience in the design, fabrication, and qualification of sterile, high-purity, and potent containment process systems is expanding its team. We deliver innovative, compliant solutions for clients in the biopharmaceutical, personal care, and food industries and are seeking talented professionals to join our growing engineering group.

We offer a dynamic, creative work environment focused on high-end engineering design projects that span the full lifecycle — from concept development to commissioning and qualification.

Position Overview

As a Process Engineer, you will play an integral role within a cross-functional engineering team, contributing to the design and delivery of GMP-compliant integrated process equipment and systems used in the manufacturing of pharmaceutical drug substances and products.

You will participate in all project phases — from conceptual and detailed design to commissioning, qualification, and validation (CQV).

Key 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 and Attributes

• Strong interpersonal and teamwork skills
• Ability to coordinate and support cross-functional project teams
• Excellent organizational and time-management abilities
• Self-motivated and capable of working independently with minimal supervision
• Strong written and verbal communication skills
• Adaptable and effective in a fast-paced, multi-tasking environment

Education and Experience

• Bachelor's degree in Engineering (Chemical, Mechanical, or related discipline)
• 3-5 years of relevant experience within the pharmaceutical or biopharmaceutical industry preferred

Location and Travel

The primary work location is in Halifax, UK, with occasional travel to partner offices and international client or vendor sites. The role will involve intermittent international assignments, including attendance at Factory Acceptance Tests (FATs) and on-site Commissioning, Qualification, and Validation (CQV) activities