Posted Friday, November 28, 2025 at 5:00 AM About OmniaBio: OmniaBio Inc. is a technology-driven, global CDMO specializing in cell and gene therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, OmniaBio leverages over a decade of expertise in regenerative medicine and advanced therapies developed in partnership with CCRM. Committed to digital transformation, OmniaBio integrates automation, robotics, and artificial intelligence into its operations to drive efficiency, enhance quality, and increase throughput. This innovative approach supports end-to-end CDMO services—from development through GMP manufacturing and scale-up—helping clients accelerate the path to market for transformative treatments. OmniaBio focuses on immune cell-based therapies, induced pluripotent stem cell therapies, and lentiviral vectors, positioning itself as a leader in advancing and maturing cell and gene therapy manufacturing. With a strategic vision to meet the surging global demand, OmniaBio aims to enable broad access to cutting‑edge therapies worldwide. Visit www.omniabio.com to learn more. Position Summary: The Director of Project Management is a project management professional who leads the project management process including governance, team leadership, tracking and monitoring, prioritization, communication, and quality controls. The Director of Project Management directs the project management office (PMO) and provides guidance and support to executives, project managers, and staff. As the operational leader of the PMO, this role is responsible for the day-to-day management and implementation of processes and methodologies. They lead project managers and ensure that projects are delivered on time, within budget, according to quality standards and the satisfaction of our clients. The initial focus of the PMO will be on client projects where this role will lead by example in driving customer satisfaction by maintaining our reputation of reliability, integrity, flexibility/collaboration, and on-time delivery. Responsibilities: Governance Framework Defines the PMO’s purpose, scope, and authority within the organization. Implements and executes the PMO, by helping establish a clear vision including interim milestones and long-term measures of success / key performance indicators. Defines the appropriate standards of governance and ownership of the project delivery lifecycles including decision-making processes. Develops systems for project selection and prioritization aligned with the organizational goals. Project Management Methodology Standardizes Project Management systems and processes by creating new or improving current processes and coordinates organizational procedures for optimized efficiency and productivity. Develops the PMO tools and resources to adaptably manage a portfolio of transformational projects with predictable consistency, efficiency, and success. Consults with clients and internal cross‑functional teams to review project proposals, statements of work, change orders, issue resolution etc. to determine scope, goals, timeframes, budget, staffing requirements and project constraints. Drives the adoption and implementation of project and program management methodologies. Resource Management Builds and leads the PMO structure, program, and team within OmniaBio, spanning multiple manufacturing facilities. Provide training to project managers to ensure standards are maintained at all times. Works collaboratively with the Business Development Team and internal stakeholders Establishes resource allocation processes ensuring optimal utilization of human and financial resources. All other duties as assigned. Qualifications: Bachelor’s degree in Business, Management or a related field Experience in Project Management within a PMO structure. Experience in Project Management in a Health Sciences field. 10+ years managing a PMO. 10+ years in Project Management 10+ years leading and managing teams. PMP certification required. Client management experience required; global client management experience an asset. Desired Characteristics: Excellent communication skills Excellent planning and organization skills to be able to operate at both a strategic and operational level. Experience managing complex teams. Experience managing a wide range of projects and programs. OmniaBio is a developing organization and represents a fluid working environment. Flexibility and adaptability are essential, and duties will be influenced by the needs of the organization. Applicants must be legally eligible to work in Canada. An applicant’s compensation package is finalized once the interview process is concluded and accounts for the nature of the role as well as the experience, competencies (job knowledge, skills and abilities) of the applicant and internal equity. OmniaBio is committed to accessibility, diversity, and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process, providing the applicant has met the bona fide requirements for the open position. Applicants should make their requirements known once contacted to schedule an interview, or when the job offer has been made. #J-18808-Ljbffr
A leading biotech company in Hamilton, Ontario is seeking a Director of Project Management to oversee the PMO, ensuring project delivery aligns with organizational goals. The role requires more than 10 years of project management experience, a Bachelor’s degree, and a PMP certification. Candidates should demonstrate excellence in communication and organizational skills, along with the ability to manage complex teams and diverse projects. This position emphasizes client satisfaction and operational efficiency. #J-18808-Ljbffr
Posted Friday, January 16, 2026 at 5:00 AM | Expires Saturday, January 31, 2026 at 4:59 AM
About OmniaBio:
OmniaBio Inc. is a technology-driven, global CDMO specializing in cell and gene therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, OmniaBio leverages over a decade of expertise in regenerative medicine and advanced therapies developed in partnership with CCRM. Committed to digital transformation, OmniaBio integrates automation, robotics, and artificial intelligence into its operations to drive efficiency, enhance quality, and increase throughput. This innovative approach supports end‑to‑end CDMO services—from development through GMP manufacturing and scale‑up—helping clients accelerate the path to market for transformative treatments. OmniaBio focuses on immune cell‑based therapies, induced pluripotent stem cell therapies, and lentiviral vectors, positioning itself as a leader in advancing and maturing cell and gene therapy manufacturing. With a strategic vision to meet the surging global demand, OmniaBio aims to enable broad access to cutting‑edge therapies worldwide. Visit www.omniabio.com to learn more.
Active Vacancy
Position summary
The Senior Financial Analyst is responsible to ensure effective delivery of high‑quality financial support and information to senior management to enable informed decision making that will ultimately improve performance, as well as enhance and develop business strategy and planning. This role will enable accurate business management, tracking, analysis, and management reporting to both internal and external stakeholders. The successful candidate will be a well‑organized individual who can set and manage various stakeholders’ expectations and is able to drive continuous improvements in a fast‑paced environment.
Key responsibilities
The employee’s services include, but are not limited to, the following:
Work with project managers to develop project‑level budgets and forecasts for multiple business functions and units.
Managing the corporate financial reporting process, including preparation of consolidated financial statements and quarterly reports to the board and other stakeholders.
Leading financial reporting projects, such as implementation of changes in accounting standards.
Be a key partner to business units and the functional teams/leaders in support of their mandates. Support business decision making through consultations with functional leaders concerning operational or service objectives impacted by changes in OmniaBio’s annual objectives and budgetary requirements.
Support the development of business intelligence strategies and technology for monthly, quarterly, and annual financial reports, at the business unit and project level, with insightful analysis for OmniaBio’s executives and senior management within defined reporting timelines, liaising with key stakeholders for input, as necessary.
Develop an understanding of data and information flow at OmniaBio. Contribute to the development of tools, standards, and guidelines to support regular business life cycle, including customer acquisition, purchasing, project management, manufacturing operations, inventory management, financial data management, invoicing, and revenue collection process.
Make recommendations on the design, needs assessment and implementation of technological improvement, including software applications to improve upon financial analytics.
Provide decision analysis support, such as business case analysis, pricing analysis, cost estimates, contract and project profitability, customer‑level reporting, technology platform‑level reporting and other market or service segment analytics and reporting.
Develop financial analysis, key metrics, financial insight, and performance reporting to support operations in various business units.
Analyze routine financial and operational reports and prepare explanations for period variances (actual vs. budget, actual current period vs. prior periods).
Identify, research, recommend, and implement (with IT) improvements to financial system/tools and processes including emerging AI initiatives around routine and non‑routine analytics reporting cycles to ensure timely provision to business unit leaders and executive management.
Prepare analysis in support of financial reporting requirements for various stakeholders, including funding providers.
Provide business information and key metrics to external funding providers and the OmniaBio board.
Document and review finance analytics and reporting processes and controls.
Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, establishing personal networks, and participating in professional institute activities.
Other finance and business support activities, as required.
Qualifications
Bachelor’s degree in business, accounting, or data management disciplines
Designated CPA, or compensating experience
8+ years of finance analytics experience, preferably within a CDMO, life sciences organization, or manufacturing organization with increasing levels of responsibility
3+ years financial reporting experience
Proficient with the Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)
Experience with implementation and operationalization of business intelligence systems
Experience with ERP systems, SAP preferred
Desired Characteristics
Well organized
Applies logic and materiality in approach to work and problems
Ability to manage shifting priorities and meet deadlines
Analytical and insightful
Strong Excel and modelling skills
Diligent and accurate in preparing deliverables
Confident in approach
Active listener
High integrity and transparency
Collaborative, team player
Values diversity and being respectful of others
OmniaBio is a developing organization and represents a fluid working environment. Flexibility and adaptability are essential, and duties will be influenced by the needs of the organization.
Applicants must be legally eligible to work in Canada.
An applicant’s compensation package is finalized once the interview process is concluded and accounts for the nature of the role as well as the experience, competencies (job knowledge, skills and abilities) of the applicant and internal equity.
OmniaBio is committed to accessibility, diversity, and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process, providing the applicant has met the bona fide requirements for the open position. Applicants should make their requirements known once contacted to schedule an interview, or when the job offer has been made.
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A leading biotech firm in Hamilton is seeking a Senior Financial Analyst to provide high-quality financial support to senior management. Responsibilities include budget development, financial reporting, and strategic planning to enhance organizational performance. The ideal candidate has over 8 years of finance analytics experience, a Bachelor’s degree, and CPA designation. This role will work in a dynamic environment requiring adaptability and collaboration, contributing to the firm's commitment to innovative therapies. #J-18808-Ljbffr
A leading biotech company in Hamilton, Ontario is seeking a Director of Project Management to oversee the PMO, ensuring project delivery aligns with organizational goals. The role requires more than 10 years of project management experience, a Bachelor’s degree, and a PMP certification. Candidates should demonstrate excellence in communication and organizational skills, along with the ability to manage complex teams and diverse projects. This position emphasizes client satisfaction and operational efficiency. #J-18808-Ljbffr
Posted Friday, November 28, 2025 at 5:00 AM
About OmniaBio:
OmniaBio Inc. is a technology-driven, global CDMO specializing in cell and gene therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, OmniaBio leverages over a decade of expertise in regenerative medicine and advanced therapies developed in partnership with CCRM. Committed to digital transformation, OmniaBio integrates automation, robotics, and artificial intelligence into its operations to drive efficiency, enhance quality, and increase throughput. This innovative approach supports end-to-end CDMO services—from development through GMP manufacturing and scale-up—helping clients accelerate the path to market for transformative treatments. OmniaBio focuses on immune cell-based therapies, induced pluripotent stem cell therapies, and lentiviral vectors, positioning itself as a leader in advancing and maturing cell and gene therapy manufacturing. With a strategic vision to meet the surging global demand, OmniaBio aims to enable broad access to cutting‑edge therapies worldwide. Visit www.omniabio.com to learn more.
Position Summary:
The Director of Project Management is a project management professional who leads the project management process including governance, team leadership, tracking and monitoring, prioritization, communication, and quality controls. The Director of Project Management directs the project management office (PMO) and provides guidance and support to executives, project managers, and staff.
As the operational leader of the PMO, this role is responsible for the day-to-day management and implementation of processes and methodologies. They lead project managers and ensure that projects are delivered on time, within budget, according to quality standards and the satisfaction of our clients.
The initial focus of the PMO will be on client projects where this role will lead by example in driving customer satisfaction by maintaining our reputation of reliability, integrity, flexibility/collaboration, and on-time delivery.
Responsibilities:
Governance Framework
Defines the PMO’s purpose, scope, and authority within the organization.
Implements and executes the PMO, by helping establish a clear vision including interim milestones and long-term measures of success / key performance indicators.
Defines the appropriate standards of governance and ownership of the project delivery lifecycles including decision-making processes.
Develops systems for project selection and prioritization aligned with the organizational goals.
Project Management Methodology
Standardizes Project Management systems and processes by creating new or improving current processes and coordinates organizational procedures for optimized efficiency and productivity.
Develops the PMO tools and resources to adaptably manage a portfolio of transformational projects with predictable consistency, efficiency, and success.
Consults with clients and internal cross‑functional teams to review project proposals, statements of work, change orders, issue resolution etc. to determine scope, goals, timeframes, budget, staffing requirements and project constraints.
Drives the adoption and implementation of project and program management methodologies.
Resource Management
Builds and leads the PMO structure, program, and team within OmniaBio, spanning multiple manufacturing facilities.
Provide training to project managers to ensure standards are maintained at all times.
Works collaboratively with the Business Development Team and internal stakeholders
Establishes resource allocation processes ensuring optimal utilization of human and financial resources.
All other duties as assigned.
Qualifications:
Bachelor’s degree in Business, Management or a related field
Experience in Project Management within a PMO structure.
Experience in Project Management in a Health Sciences field.
10+ years managing a PMO.
10+ years in Project Management
10+ years leading and managing teams.
PMP certification required.
Client management experience required; global client management experience an asset.
Desired Characteristics:
Excellent communication skills
Excellent planning and organization skills to be able to operate at both a strategic and operational level.
Experience managing complex teams.
Experience managing a wide range of projects and programs.
OmniaBio is a developing organization and represents a fluid working environment. Flexibility and adaptability are essential, and duties will be influenced by the needs of the organization.
Applicants must be legally eligible to work in Canada.
An applicant’s compensation package is finalized once the interview process is concluded and accounts for the nature of the role as well as the experience, competencies (job knowledge, skills and abilities) of the applicant and internal equity.
OmniaBio is committed to accessibility, diversity, and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process, providing the applicant has met the bona fide requirements for the open position. Applicants should make their requirements known once contacted to schedule an interview, or when the job offer has been made.
#J-18808-Ljbffr
OmniaBio: Director, Quality Compliance (12-month contract)
Hamilton, ON, Canada
Job Description
Posted Tuesday, April 14, 2026 at 4:00 AM
About OmniaBio
OmniaBio Inc. is a technology‑driven, global CDMO specializing in cell and gene therapies, with a mission to transform biomanufacturing with AI and automation. Located at McMaster Innovation Park in Hamilton, Ontario, OmniaBio leverages over a decade of expertise in regenerative medicine and advanced therapies developed in partnership with CCRM. Committed to digital transformation, OmniaBio integrates automation, robotics, and artificial intelligence into its operations to drive efficiency, enhance quality, and increase throughput. This innovative approach supports end‑to‑end CDMO services—from development through GMP manufacturing and scale‑up—helping clients accelerate the path to market for transformative treatments. OmniaBio focuses on immune cell‑based therapies, induced pluripotent stem cell therapies, and lentiviral vectors, positioning itself as a leader in advancing and maturing cell and gene therapy manufacturing. With a strategic vision to meet the surging global demand, OmniaBio aims to enable broad access to cutting‑edge therapies worldwide. Visitwww.omniabio.com to learn more.
Active Vacancy
Position Summary
As Director, Quality Compliance, at OmniaBio, you will be responsible for 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 Manufacturing Practices (GMP) environment, along with external stakeholders and regulators. You will be a key member of the Quality Management team.
Responsibilities
Maintains a high level of expertise in GMP compliance with respect to cell and gene therapy manufacture and well as all aspects of GMP compliance.
Oversee and accountable for the corrective and preventive action (CAPA) program.
Oversee and accountable the manufacturing change control program.
Oversee and accountable for the training program to enhance OmniaBio’s right to operate and delivery to patients.
Oversee and accountable for the customer complaints program.
Accountable for the product recall program.
As a key member of the Quality team, owns and delivers the management review of the quality program and provides status updates to senior management on the overall health of the compliance program.
Oversee and accountable for the documentation program.
Implements and Accountable for the audit program (internal audits, client audits and health authority inspections).
Collaborates with IT business partners to implement the computer validation program.
Oversee and accountable for the data integrity program.
Manages the quality compliance team.
Hosts health authority and client audits.
Reviews and approves deviations, CAPA, change controls, and other quality‑related documents as required.
Ensures GMP is embedded in all manufacturing‑related tasks.
Maintains current understanding of GMPs and evolving regulations, and owns OmniaBio’s compliance standards.
Engages and supports the OmniaBio Operating Model continuous improvement philosophy.
Requirements
Bachelor of science degree in science or engineering.
10-20 years of equivalent industry experience.
Must have knowledge of compliance aspects of cell and gene production, sterile manufacture and overall GMP knowledge.
Practitioner of risk management and comfortable in the use of risk analysis tools.
Must have working experience in the delivery of biological products for commercial supply.
Excellent understanding of Health Canada/U.S. Food and Drug Administration GMP regulations and QA principles.
Desired Characteristics
Capable of managing multiple projects.
Strong presentation skills and English written and oral communication skills.
Experienced in driving results by influencing others in a highly cross‑functional environment.
Demonstrates a collaborative and enabling management style.
OmniaBio is a developing organization and represents a fluid working environment. Flexibility and adaptability are essential, and duties will be influenced by the needs of the organization.
Applicants must be legally eligible to work in Canada.
An applicant’s compensation package is finalized once the interview process is concluded and accounts for the nature of the role as well as the experience, competencies (job knowledge, skills and abilities) of the applicant and internal equity.
OmniaBio is committed to accessibility, diversity, and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process, providing the applicant has met the bona fide requirements for the open position. Applicants should make their requirements known once contacted to schedule an interview, or when the job offer has been made.
#J-18808-Ljbffr
Champion compliance excellence in cell and gene therapy manufacturing. Manage strategic programs to ensure GMP adherence and improve operational efficiencies.
As the Director of Quality Compliance, you will oversee compliance initiatives in a dynamic biomanufacturing setting. This leadership role focuses on managing external audits, CAPA programs, and employee training in line with GMP standards. Your collaboration with various stakeholders will ensure quality and safety in every aspect of production.
Key Responsibilities:
• Direct the CAPA and change control processes
• Manage complaints and product recall systems
• Lead the documentation and training programs
• Implement validation and audit strategies
• Facilitate health authority and client audits
Requirements:
• Bachelor’s degree in science or engineering
• 10–20 years of relevant experience required
• Strong knowledge of compliance in biological production
• Expertise in Health Canada and FDA regulations
• Proficient in risk management strategies
Drive compliance advancements in cell and gene therapies, optimizing quality management practices for better outcomes.
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