• Delivers quality control-related services, including sample management, testing, method development, optimization, qualification and validation, stability program, data review and equipment management.
• Complies with all standard operating procedures (SOPs) and work practices.
• Maintains the materials specification program, as directed.
• Releases materials, as directed.
• Manages the retain and reference standard program, as directed.
• Adheres to the QC documentation quality management system program, including SOPs, logbook and associated forms.
• Maintains the sample management program, including sample identification, storage and retention.
• Performs material testing in compliance with approved and current specifications, including but not limited to, incoming materials, in-process materials, drug substance materials, drug product materials, environmental monitoring samples, and stability samples, as required.
• Participates in internal audits and/or supplier audits, as required.
• Participates in client audits and health authority audits, as required.
• Collaborates with the Facilities and Engineering team to ensure that facilities are available for production, including but not limited to, room readiness and environmental monitoring data.
• Reviews and assesses deviations, corrective and preventative actions, change controls, etc.
• Continuously grows and adapts in a fast-moving field to keep yourself and the organization at the forefront of the cell and gene therapy and regenerative medicine fields.
• Ensures GMP is embedded in all manufacturing related tasks.
• Engages and supports the OmniaBio Operating Model continuous improvement philosophy.

Requirements

• High school diploma, college diploma preferred.
• 1-2 years of experience in cell therapy/viral quality control department supporting GMP production, or similar within the pharmaceutical, medical technologies, biologics or similar industries.
• Experience working for a CDMO, a third-party testing facility or a biotechnology company performing similar activities.
• Strong understanding of cell manufacture processes and technologies.
• Excellent understanding of Health Canada/US Food and Drug Administration GMP regulations and quality assurance principles.

Desired Characteristics

• Sound knowledge of applicable regulatory frameworks and requirements for cell and gene therapy and regenerative medicine, such as GMP, ISO, or medical device development.
• Independent, detail-oriented self-starter with excellent analytical skills and able to multitask and succeed in a team environment.
• Experience establishing customer-facing organizations and service models.
• Demonstrated initiative and the ability to deliver high-quality outcomes.

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.