Job Title

Process Engineer***The successful candidate must be willing to live in Toronto Canada for the first 12 months.***All expenses covered;FlightsHousingCarFixed per diem (amount TBD) for food and miscellaneous daily incidentalsA 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 OverviewAs 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 ResponsibilitiesUnder the guidance of senior engineers, responsibilities will include:Developing design bases and evaluating process alternativesPreparing User Requirement Specifications (URS)Creating Process Flow Diagrams (PFDs) and Piping & Instrumentation Diagrams (P&IDs)Integrating process unit operations and designing equipment layoutsSizing and specifying process equipmentSupporting commissioning and qualification protocol development and executionSkills and AttributesStrong interpersonal and teamwork skillsAbility to coordinate and support cross-functional project teamsExcellent organizational and time-management abilitiesSelf-motivated and capable of working independently with minimal supervisionStrong written and verbal communication skillsAdaptable and effective in a fast-paced, multi-tasking environmentEducation and ExperienceBachelor’s degree in Engineering (Chemical, Mechanical, or related discipline)3–5 years of relevant experience within the pharmaceutical or biopharmaceutical industry preferredLocation and TravelThe 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.