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Department: Facilities and Engineering Position Summary As Technician II, Facilities Maintenance, you will be a key part of the OmniaBio team, responsible for the execution of work orders and preventive maintenance (PM) orders to support current Good Manufacturing Practices (GMP) activities. The role is located at OmniaBio’s Hamilton, Ontario, facility and is site-based, to support 24/7 manufacturing activities. The Technician II, Facilities Maintenance, will share routine on-call cover ...Read more about OmniaBio: Technician II, Facilities MaintenanceMore
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Department: Facilities and Engineering Position Summary As Technician II, Facilities HVAC (Heating, Ventilation and Air Conditioning), you will be a key part of the OmniaBio team and will be primarily responsible for the execution of all HVAC and related work orders and preventive maintenance (PM) activities in support of Good Manufacturing Practices (GMP) activities. The position is located at OmniaBio’s Hamilton, Ontario, facility and is site-based, to support 24/7 manufacturing activit ...Read more about OmniaBio: Technician II, Facilities HVACMore
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Department: Facilities and Engineering Position Summary As Manager, Commissioning, Qualification and Validation (CQV), you will manage CQV activities such as the development of a validation master plan(s), and qualification/validation of deliverable(s) and standard operating procedures (SOPs). The person in this position provides leadership in a first-line management capacity by training, mentoring and supervising CQV staff to complete projects and departmental goals safely, efficiently an ...Read more about OmniaBio: Manager, CQVMore
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Department: Facilities and Engineering Position Summary The Associate I, Commissioning, Qualification and Validation, supports activities including development of validation master plan(s), and qualification/validation of deliverable(s) and standard operating procedures (SOPs). Responsibilities include assessment and development of qualification documentation for the facility, equipment, and systems, and ensuring the documentation and equipment is compliant for manufacture to Good Manufa ...Read more about OmniaBio: Associate II, CQVMore
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Department: Supply Chain Position Summary: As Director, Supply Chain(SC) , you will be highly experienced in leading SC teams in a cell and gene therapy (CGT) manufacturing facility. The person in this role will lead a high-performing department focused on SC and logistics projects adhering to Good Manufacturing Practices (GMP). The position is located at OmniaBio’s Hamilton, Ontario facility. The role is site-based and may involve some work outside of normal workday hours. The person ...Read more about OmniaBio: Supply Chain DirectorMore
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Reports to: Vice President, Quality Assurance & Regulatory Compliance Department: Quality Position Summary: As Manager, External Quality at OmniaBio, you will be responsible for designing, implementing and managing the external quality program within a cell and gene therapy manufacturing facility. You will design, implement and manage the supplier and material management program. The role will liaise closely with all functions operating in the Good Manufacturing Practices (GMP) ...Read more about OmniaBio: Manager, External QualityMore
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Department: Supply Chain Position Summary: As Associate II, Supply Chain, you will be experienced in the supply chain needs of a manufacturing facility. The role will be part of a high-performing team focused on supply chain and logistics projects adhering to Good Manufacturing Practices (GMP). The location of this position is at OmniaBio’s Hamilton, Ontario, facility. This position is site-based, with work hours adhering to a designated pattern of 12-hour shifts. The primary role is t ...Read more about OmniaBio: Associate II, Supply ChainMore
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Department: Quality Control Position Summary: As the Associate II, Quality Control, at OmniaBio, you are an experienced individual in the field of quality control (QC) for Good Manufacturing Practices (GMP) manufacturing of cell and gene therapy products, driven by the opportunity to enable clinical translation of cell therapy and regenerative medicine. The Associate II, Quality Control, will be required to work across the entire range of activities, including but not limited to, testin ...Read more about OmniaBio: Associate II, Quality ControlMore
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Department: OmniaBio Operations Position Summary: As a Manufacturing Manager at OmniaBio, you will be experienced in cell and gene therapy manufacturing and leading teams. The person in this role will provide leadership for multiple shift-based manufacturing teams focused on production projects adhering to Good Manufacturing Practices (GMP) based at OmniaBio’s Hamilton, Ontario, facility. The primary purpose of this role is to lead manufacturing activities working closely with clients and other ...Read more about OmniaBio: Manager, ManufacturingMore
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Reports to: Vice President, Quality Assurance & Regulatory Compliance Department: Quality Position Summary: As Manager, Manufacturing Quality Assurance at OmniaBio, you will be responsible for designing, implementing and managing a manufacturing quality program within a cell and gene therapy manufacturing facility. You will provide quality oversight for the manufacturing operations and the supporting components such as facility and equipment readiness. The person in this role will ...Read more about OmniaBio: Manager, Manufacturing Quality AssuranceMore
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Reports to: Vice President, Quality Assurance and Regulatory Compliance Department: Quality Position Summary: As Director, Quality Compliance, at OmniaBio, you will be responsible for designing, implementing and managing the overall compliance program within a cell and gene therapy manufacturing facility. You will provide strategic and tactical direction on the key compliance programs for OmniaBio. The role will liaise closely with all team members operating in the Good Manufactu ...Read more about OmniaBio: Director, Quality ComplianceMore
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Position Summary:As the Manager, Sterility Assurance at OmniaBio, you will be responsible for designing, implementing and managing a sterility assurance and contamination control program within a cell and gene therapy manufacturing facility. You will provide technical expertise to define and execute the project plan and the ongoing support of the program. The person in this role will liaise closely with the Environmental Monitoring (EM) team embedded within the Quality Control (QC) department. Y ...Read more about OmniaBio: Sterility Assurance ManagerMore
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Position Summary: As a Manufacturing Supervisor at OmniaBio, you will be experienced in cell and gene therapy manufacturing and leading small teams. The person in this role will be a leading member of a high performing team focused on production projects adhering to Good Manufacturing Practices (GMP). This role is site-based at OmniaBio’s location in Hamilton, Ontario, and involves working regularly scheduled 12-hour shifts. The primary purpose of this role is to lead the shift-based team in th ...Read more about OmniaBio: Manufacturing SupervisorMore
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Role Summary: The Procurement Specialist II is responsible for assisting in operating an effective and efficient procurement & supply chain function for the organization and its affiliates. Reporting to the Sr Manager, Supply Chain and Procurement, the Procurement Specialist will help optimize procurement processes, inventory management and reporting, and ensure effective controls are in place, supporting corporate strategy and business operations. Responsibilities: Supports the implementati ...Read more about OmniaBio: Procurement Specialist IIMore
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Canada ● Req #228Tuesday, January 30, 2024Role Summary: Reporting to the Chief Information Officer (CIO) of CCRM and OmniaBio, the Senior Director, IT - Commercial Systems, Data and Analytics (CDA) will lead a team focused on selecting, implementing and supporting systems related to business development, master data management and analytics. Focus areas will include sales and marketing automation, deal flow, sales coaching, customer-facing applications, data governance, reporting/dashboarding and artificial analytics. The Senior Directo ...Read more about OmniaBio: Senior Director, IT - Commercial Systems, Data and AnalyticsMore
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Position Summary:As a Manufacturing Associate II at OmniaBio, you will be experienced in biologics manufacturing. The person in this role will be part of a high-performing team focused on production projects adhering to Good Manufacturing Practices (GMP) at OmniaBio’s Hamilton, Ontario, facility. This position is site-based, with work hours adhering to a designated pattern of 12-hour shifts. The primary function of this role is to execute manufacturing activities in support of OmniaBio’s client ...Read more about OmniaBio: Manufacturing Associate IIMore
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Role Summary: Reporting to the Senior Director, IT-GMP Systems, the Manager, Master Data Governance is responsible for managing and governing all enterprise master data and associated processes; and ensuring data accuracy, completeness and compliance with corporate policies and regulatory requirements (privacy, security and Good Manufacturing Practices (GMP)). Responsibilities: Develops, implements and maintains master data governance policies and procedures to ensure the accuracy, completene ...Read more about OmniaBio: Manager, Master Data GovernanceMore
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Canada ● Req #223Friday, January 26, 2024Job Title: Business Process Manager, FICO Role Summary: The Business Process Manager (BPM), Finance/Controlling (FI/CO), reports to the Head of IT Manufacturing. The BPM FI/CO evaluates, designs, executes, measures, monitors, and controls financial and controlling business processes relating to the end-to-end value chain, accounts payable, accounts receivable, financial accounting, management accounting, fixed asset accounting, treasury, cost centre accounting, profitability analysis, inter-co ...Read more about OmniaBio: Business Process Manager, Finance/Controlling (FICO)More
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