Job Title

COMPANY OVERVIEW:Prollenium Medical Technologies Inc. is a fast-growing Canadian developer, manufacturer and international distributor of premium HA dermal filler. We are proud to address all of our client's needs through streamlined medical device innovation. Prollenium is able to ensure a continual flow of creation, unique ideas, and a steady pipeline of new and exciting products that provide safe and effective results. US FDA, Health Canada, and CE approvals, over 4 million syringes in the Revanesse product line have been sold to 80+ countries world-wide. Prollenium is the only manufacturer of Hyaluronic Acid dermal fillers in North America. Join our dedication to innovation.Prollenium provides competitive compensation, benefits, and development opportunities.POSITION OVERVIEW:The Project Engineer will support and manage engineering and construction projects across Prolleniums manufacturing and facility operations. This role involves planning, executing, and overseeing capital and infrastructure projects, including facility layouts, HVAC, utilities, and water systems - ensuring compliance with applicable regulations and industry standards.KEY RESPONSIBILITIES:Lead capital and infrastructure projects including facility expansions, cleanroom builds, HVAC and utility upgrades, equipment installations and process area redesigns.Oversee engineering design, layout, and technical documentation, ensuring projects meet safety, quality, and GMP standards.Manage contractors, consultants, and vendors to ensure on-time and within-budget delivery.Conduct technical assessments, feasibility studies, and risk analyses to support project planning and decision-making.Lead commissioning, qualification, and validation activities for facilities and utilities.Ensure compliance with GMP, GEP, EHS, and regulatory standards (Health Canada, FDA).Support facility master planning and continuous improvement initiatives to enhance reliability and efficiency.Provide technical expertise and troubleshooting for facility systems such as HVAC, purified water, and compressed air.Collaborate cross-functionally with Operations, Quality, and Validation teams.MINIMUM QUALIFICATIONS:Technical Knowledge / Experience:Bachelors degree in Mechanical, Electrical, or Industrial Engineering (or a related field).Minimum 5+ years of project engineering experience in a regulated manufacturing environment (pharma, biotech, or medical devices preferred).Strong technical knowledge of HVAC, cleanroom design, water systems, and facility construction.Proven track record managing capital projects from design through start-up.Skilled in AutoCAD and project management tools (e.g., Microsoft Project).Excellent communication, organization, and leadership skills.Strong understanding of GMP, validation, and regulatory requirements.P.Eng designation (desirable)Behavioral:Takes ownership of projects and results.Works effectively with cross-functional teams and partners.Ensures accuracy and quality in all technical work.Responds positively to changing priorities and challenges.Proactively identifies and drives improvements.