Explore 10 Jobs at Applied Pharmaceutical Innovation (API)
Open Positions at Applied Pharmaceutical Innovation (API)
Posted a month ago
The Administrator, Quality Assurance supports pharmaceutical quality systems, including document and record management, training administration, change control, risk assessments, and deviation investigations with CAPA implementation. The role also reviews GMP records and analytical data, supports audits and quality initiatives, and collaborates with internal teams and stakeholders; it requires full-time on-site presence in Edmonton and travel between API sites.
Key Details
- full time Jobs
- 3+ years experience
Top Skills Required
Top Benefits
Posted 2 months ago
The Specialist, Compliance supports GMP compliance for pharmaceutical and sterile injectable manufacturing operations. Responsibilities include managing production and equipment documentation, reviewing records, coordinating deviations, investigations, CAPA, change controls, qualification and validation activities, audits, training, and inspection readiness. The role is full-time on-site in Edmonton and requires collaboration across Production, Quality Assurance, Engineering, Validation, Quality Control, and Technical Operations.
Key Details
- full time Jobs
- 3+ years experience
Top Skills Required
Top Benefits
Posted 2 months ago
The Production Operator performs active pharmaceutical ingredient manufacturing activities in a GMP-regulated environment, including chemical processing, equipment operation, material handling, cleaning, sampling, and production documentation. The role also supports quality and compliance activities, equipment maintenance, validation, inventory management, safety requirements, and shift handovers while working full-time on site and rotating shifts.
Key Details
- full time Jobs
- 3+ years experience
Top Skills Required
Top Benefits
Posted 3 months ago
The Coordinator, Facilities Maintenance supports maintenance and calibration coordination for GMP manufacturing and laboratory facilities. The role manages schedules, work orders, records, asset information, inspections, compliance readiness, and equipment performance monitoring while collaborating with internal teams and service providers.
Key Details
- full time Jobs
- 1+ years experience
Top Skills Required
Top Benefits
Posted 3 months ago
The Specialist, Quality Control - Equipment & Systems manages the lifecycle, qualification, and technical support of analytical laboratory instruments and computerized systems within a GMP-compliant QC laboratory. Responsibilities include equipment management, method validation/transfer, LIMS administration, regulatory compliance, and HSE lab responsibilities. This is a temporary full-time role (20-month term) with potential extension.
Key Details
- contract Jobs
- 3+ years experience
Top Skills Required
Top Benefits
Posted 3 months ago
This role involves hands-on engineering support for the installation, commissioning, qualification, and validation of GMP manufacturing equipment and facilities in a pharmaceutical environment. The position requires practical experience in equipment reliability, troubleshooting, and operational support, with a focus on ensuring compliance and validation readiness throughout the equipment lifecycle.
Key Details
- full time Jobs
- 3+ years experience
Top Skills Required
Top Benefits
Posted 3 months ago
This role involves hands-on maintenance, troubleshooting, and repair of GMP manufacturing equipment and facility systems for a pharmaceutical production facility. The position supports equipment lifecycle activities, including commissioning, preventative maintenance, and continuous improvement, while ensuring compliance with regulatory standards.
Key Details
- full time Jobs
- 3+ years experience
Top Skills Required
Top Benefits
Posted 4 months ago
This role is responsible for building and owning the integrated planning, supply chain, and program costing functions from the ground up at a life sciences CDMO. The Head of Integrated Planning will manage demand forecasting, GMP materials procurement, capacity planning, and end-to-end program cost modeling to ensure accurate resource allocation, scheduling, and profitability for drug development and manufacturing programs.
Key Details
- full time Jobs
- 8+ years experience
Top Skills Required
Top Benefits
Posted 4 months ago
The Vice President of Finance will lead the finance function, overseeing budgeting, forecasting, financial reporting, and treasury operations for Applied Pharmaceutical Innovation. This executive role partners closely with the CEO and senior leadership to drive financial strategy, secure funding, and ensure compliance while supporting the organization’s growth in the life sciences sector.
Key Details
- full time Jobs
- 12+ years experience
Top Skills Required
Top Benefits
Posted 5 months ago
The Manager, CQV (Installation, Commissioning, Qualification and Validation) will lead critical construction, installation, and CQV activities for the new Critical Medicines Production Centre (CMPC) in Edmonton, Alberta. This role involves overseeing GMP-compliant manufacturing facility setup, ensuring technical alignment with project requirements, and managing qualification and validation processes for complex pharmaceutical systems.
Key Details
- full time Jobs
- 5+ years experience
Top Skills Required
Top Benefits
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