Director of Internships

3 weeks ago

Hamilton ON, Canada OmniaBio Full time

Reports to: Vice President, Quality Assurance and Regulatory Compliance
Department: Quality

ca), a leader in developing and commercializing regenerative medicine-based technologies and cell and gene therapies. OmniaBio’s facility will be Canada’s first commercial-scale contract development and manufacturing organization (CDMO) dedicated to cell and gene therapies and is expected to be the largest facility of its kind in Canada.

Based at McMaster Innovation Park in Hamilton, Ontario, OmniaBio will anchor a biomanufacturing centre of excellence and open in three phases between 2024 and 2026. Benefitting from CCRM’s existing expertise and business practices, OmniaBio currently has established process and analytical development teams and contract manufacturing capabilities. The vision is to provide focused support for clients with late clinical-stage manufacturing and commercial supply needs, in addition to early-stage development and first in-human clinical trial material services. 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. You will be a key member of the Quality Management team.

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.
Designs, creates, implements and maintains the manufacturing change control program.
Designs and delivers training to appropriate personnel as required to enhance OmniaBio’s right to operate and delivery to patients.
Designs, creates, implements and maintains the customer complaints program.
As a key member of the Quality Assurance (QA) 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.
Designs, creates, implements and maintains the product documentation and training programs.
Collaborates with IT business partners to implement the computer validation program.
Designs, creates, implements and maintains the data integrity program.
Manages the quality compliance team.
Reviews and approves deviations, CAPA, change controls, and other quality-related documents as required.
Maintains current understanding of GMPs and evolving regulations, and owns OmniaBio’s compliance standards.
Bachelor of science degree in science or engineering.
~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.
~ Food and Drug Administration GMP regulations and QA principles.


Capable of managing multiple projects.
Strong presentation skills and English written and oral communication skills.
Demonstrates a collaborative and enabling management style.

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.

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