6 дней назад
Maintenance Manager (Biopharma Manufacturing)
76 200 - 110 100CAD
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Maintenance Manager (Biopharma Manufacturing): Leading safe, compliant, and efficient maintenance execution across utilities, facilities, infrastructure, and production support systems in a GMP-regulated manufacturing site with an accent on asset reliability, CMMS discipline, and shutdown coordination. Focus on allocating resources, resolving equipment and system issues, coordinating contractors, and maintaining operational continuity across production and engineering teams.
Location: Toronto, ON, Canada; onsite
Salary: CAD 76,200–110,100 per year
Company
is an R&D-driven biopharmaceutical company developing medicines and vaccines through science, manufacturing, and innovation.
What you will do
- Lead preventive and corrective maintenance across utilities, HVAC, refrigeration, electrical and mechanical systems, infrastructure, and building systems.
- Supervise maintenance teams and contractors, coordinating daily and weekly work plans and documenting execution in SAP/iShift CMMS.
- Partner with Production, Engineering, Quality, Reliability, and Supply Chain to support production schedules and minimize downtime.
- Coordinate shutdown readiness, scope alignment, resource allocation, commissioning, and asset handovers.
- Monitor maintenance performance, backlog, schedule adherence, risks, and mitigation actions.
- Drive troubleshooting, Lean continuous improvement, CMMS enhancements, and compliance with GMP and HSE requirements.
Requirements
- Diploma or degree in Mechanical, Electrical, Chemical, Industrial Engineering, or a related field, or equivalent experience.
- Minimum 3 years of relevant maintenance planning and scheduling experience.
- Strong maintenance planning and scheduling experience in a manufacturing environment, including required shutdown planning and coordination.
- Strong knowledge of SAP PM or an equivalent CMMS.
- Understanding of maintenance planning, scheduling, resource allocation, and GMP/HSE compliance.
- Strong organizational, communication, stakeholder management, and prioritization skills.
Nice to have
- Professional Engineer license in Ontario or membership in a relevant professional association such as OACETT.
- Process engineering experience.
- Experience in pharmaceutical or biotech manufacturing.
Culture & Benefits
- Full-time, fixed-term assignment for 18 months.
- Health and wellbeing benefits, including healthcare, prevention, and wellness programs.
- Career development opportunities through promotion or lateral international moves.
- Supportive, future-focused environment centered on safety, inclusion, and scientific progress.
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