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Senior Aseptic Filling Project Engineer

Arnprior, Ontario, Canada
Senior Level
Full-Time

About the role

Senior Aseptic Filling Project Engineer

Pillar5 Pharma is seeking an experienced Senior Project Engineer / Senior Aseptic Filling Engineer to lead the implementation of new aseptic manufacturing and packaging capabilities within our growing sterile ophthalmic manufacturing operations. This role is responsible for managing complex capital projects from concept through commercial production, ensuring new equipment, systems, and processes are successfully designed, installed, commissioned, validated, and transitioned into operation. Working closely with Quality, Validation, Manufacturing, Maintenance, and Operations, the successful candidate will support the expansion of Pillar5's aseptic manufacturing capabilities while driving improvements in capacity, reliability, compliance, and operational performance.

RESPONSIBILITIES

Lead engineering projects related to aseptic filling, packaging, sterilization systems, equipment upgrades, and facility expansion initiatives. Manage all phases of project execution including scope development, budgeting, scheduling, procurement, installation, commissioning, validation, startup, and handover to Operations. Develop and maintain project plans, ensuring alignment with operational, quality, validation, regulatory, and business requirements. Prepare and manage engineering documentation including URS, FDS, SOPs, work instructions, change controls, engineering assessments, and technical procedures. Coordinate equipment design reviews and manage relationships with vendors, contractors, suppliers, and system integrators. Support and oversee FAT, SAT, DQ, IQ, OQ, commissioning, and validation activities for new and modified equipment. Provide technical leadership and troubleshooting support for aseptic filling, packaging, sterilization, and related manufacturing systems. Support the implementation, operation, and optimization of aseptic processing technologies, including Open and Closed RABS systems. Drive continuous improvement initiatives focused on equipment reliability, efficiency, throughput, and overall equipment effectiveness (OEE). Participate in deviations, investigations, root cause analysis, CAPAs, and change management activities. Ensure compliance with GMP, regulatory, safety, and engineering standards throughout all project phases. Collaborate with Quality, Validation, Manufacturing, Maintenance, and Operations teams to ensure successful project delivery and ongoing operational performance.

QUALIFICATIONS AND REQUIREMENTS

Degree or Diploma in Mechanical Engineering, Manufacturing Engineering, or a related engineering discipline. P.Eng designation or eligibility for professional registration is preferred. Minimum 10 years of engineering and project management experience within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments. Demonstrated experience leading capital projects, equipment installations, production line expansions, and facility retrofit initiatives. Strong knowledge of aseptic filling, packaging, sterilization systems, and sterile manufacturing operations. Experience working in GMP-regulated cleanroom environments, including contamination control, environmental monitoring, and Grade A/B aseptic processing. Practical experience with Open and Closed RABS systems and aseptic manufacturing technologies. Experience preparing and reviewing engineering documentation, including URS, qualification protocols, and validation deliverables. Working knowledge of equipment qualification and validation activities including FAT, SAT, DQ, IQ, OQ, and commissioning. Proficiency with AutoCAD, Microsoft Project, and Microsoft Office Suite. Strong troubleshooting, problem-solving, project management, and cross-functional leadership skills. Knowledge of GMP, FDA, ISO, and regulatory compliance requirements. Experience working with OEMs, contractors, system integrators, and external vendors. Familiarity with PLC-controlled systems, automation integration, and manufacturing process equipment is considered an asset.

Compensation

The salary range for this role is $110,000 - $145,000.

APPLICATION PROCESS

This posting is for an existing vacancy. Pillar5 Pharma does not use AI at any stage of the recruitment or hiring process. Pillar5 Pharma is committed to diversity, inclusion, and equal opportunity in the workplace. Accommodations are available upon request throughout the recruitment and selection process.

About Pillar5 Pharma Inc.

Pharmaceutical Manufacturing
51-200
Founded in 2009

Founded in 2009, Pillar5 Pharma Inc. has grown to become an industry leading Canadian Contract Development and Manufacturing Organization (CDMO) across the North American Market. Pillar5 provides access to safe medications, through various partners, in solid dose tablets/capsules and Ophthalmics.

The team at Pillar5 has proven experience in formulation and process development in the laboratory, the manufacturing environment, and on the plant floor. Pillar5 is currently the only CDMO with the ability to manufacture multi-dose preservative free solutions.

Built by Pfizer in 1956, Pillar5 has an award-winning manufacturing facility that has been instrumental to the company's continued growth and success, located in the small town of Arnprior, ON. This facility has been successfully inspected by Health Canada in 2013 and the FDA in 2013 (no 483’s).

Pillar5 runs on the foundation of these 5 pillars: Speed, Flexibility, Quality, Customer Service, and Reliability, and we work to achieve these every day.

Visit: http://www.pillar5pharma.com or contact us at 1-613-623-4221

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