Hamilton On Biotechnology Jobs – 11 Openings This Week

OmniaBio: Microbiologist
Centre for Commercialization of Regenerative Medicine —Hamilton, ON
- $65,000–$75,000 a year
- Full-time
- Analysis skills
- Bachelor's
Quick apply
14d
QC Analyst
AtomVie Global Radiopharma Inc. —Hamilton, ON
- From $60,000 a year
- Weekends as needed
- Microsoft Excel
- Heavy lifting
- English
- Dental care
- Employee assistance program
Quick apply
Analytical Development Chemist
AtomVie Global Radiopharma Inc. —Hamilton, ON
- $70,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Doctoral degree
- Dental care
- Employee assistance program
Quick apply
Sr. Embryologist
True Care Fertility —Hamilton, ON
- Weekends as needed
- Laboratory experience
- Master's degree
- Supervising experience
Quick apply
Healthcare CANADA Quality Assurance & Regulatory Affairs Senior Director
UPS —Burlington, ON
- Up to $237,000 a year
- Full-time
- Project management
- Bachelor's
- Travel
Sourcing Specialist
Thermo Fisher Scientific —Burlington, ON
- $76,400–$114,575 a year
- Full-time
- Microsoft Excel
- Inventory management
- ERP systems
Trial Delivery Management (Advanced)
ICON Plc —Burlington, ON
- Full-time
- Project management
- Bachelor's
- Travel
- Disability insurance
- Dental care
1d
Enterprise Architect (Business Technology Architect) - Life Sciences
Capgemini —Burlington, ON
- $98,497–$255,000 a year
- Azure
- Computer Science
- Engineering
- Disability insurance
- Dental care
1d
Account Manager
AtomVie Global Radiopharma Inc. —Hamilton, ON
- From $100,000 a year
- Full-time
- PMP
- Sales
- Writing skills
- Dental care
- Employee assistance program
Quick apply
Associate Director, Clinical Operations (Study Startup)
Everest Clinical Research —Canada
- $165,000–$210,000 a year
- Remote
- Management
- Up to 50% travel
- Master's degree
- Disability insurance
- Dental care
Quick apply

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Quality Engineer/ Analyst
AVL Manufacturing Inc. —Hamilton, ON
Strong understanding of mechanical drawings and specifications. Ability to interpret engineering drawings and standards. Root Cause & Corrective Action.
$70,000–$85,000 a year
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Quality Control Analyst
Quantum Management Services —Brantford, ON
Experience with OOS investigations, deviations, and SOP development/review. Strong knowledge of GMP and regulatory compliance requirements.
$30 an hour
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6d

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Clinical Trial Assistant I
Everest Clinical Research —Markham, ON
Interact with study Sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high-quality operationalization of clinical…
$45,000–$65,000 a year
Quick apply
Clinical Data Management Specialist
Everest Clinical Research —Markham, ON
A Bachelors’ or Masters’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields.
$45,000–$70,000 a year
Quick apply

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OmniaBio: Microbiologist

Centre for Commercialization of Regenerative Medicine -
Hamilton, ON

Quick apply

Job details

Full-time
$65,000–$75,000 a year
14 days ago

Qualifications

Analysis skills
Bachelor's

Full job description

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:
As the Microbiologist at OmniaBio, you are an experienced individual in the field of Microbiology for Good Manufacturing Practices (GMP) manufacturing. The Microbiology EM team is responsible for all aspect of quality for the organization with respect to Environmental Monitoring and Aseptic Process Simulation (APS) visual inspection. Microbiologist will be required to work across the entire range of activities, including but not limited to maintaining the environmental conditions in our clean rooms by performing environmental monitoring, testing, sample management, equipment qualification, method suitability and data review and APS visual inspection and growth promotion. You will demonstrate flexibility within the quality and larger organization, flowing to work priorities as required. Environmental monitoring (EM) is an enabling function and as such this role will support production and facility needs to ensure product supply to patients. You will ensure the high-quality delivery of contract services.

Responsibilities:

Deliver quality control microbiology related services including, environmental monitoring, sample management, testing, method suitability, data review and equipment management.
Collaborate with Production, Manufacturing Science and Technology (MSAT), Facilities and QC in the preparation of environmental monitoring strategy and execution.
Maintain the EM schedule.
Perform 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.
Design, organize and maintain the Standard Operating Procedures (SOPs) that describe our equipment’s key functions including operations and maintenance procedures.
Facilitate the training of end-users on sampling requirements, sample handling and other quality procedures (if applicable).
Create equipment log-books/records and a Preventative Maintenance (PM) schedule for applicable equipment.
Review and approve Microbiology documentation as required.
Maintain the sample management program, including sample identification, storage and retention.
Facilitate the third-party testing by our approved partners and support the qualification processes (as needed) of third-party laboratories.
Perform aseptic gowning qualification and maintain personnel qualifications.
Provide in-suite and on the floor support for OmniaBio’s manufacturing teams, ensuring a compliant and fast to patient mindset. Plan and execute EM sampling for all in-suite activities. Collaborate with production, QC and Facility peers, to co-create solutions to remediate compliance and quality issues.
Perform room status update, in collaboration with client, ensure all EM documentation is complete and available for approval.
Participate in Client audits and Health Authority audits as required.
Prepare, review and assess deviations, corrective and preventative actions (CAPA), Change Controls, etc.
Provide quality support for clients and third-party contract services when needed.
Ensure GMP is embedded in all manufacturing related tasks.
Engage and support the OmniaBio Operating Model (OBOM) continuous improvement philosophy.
Continuously grow and adapt in a fast-moving field to keep yourself and the organization at the forefront of the cell and gene therapy and regenerative medicine fields.
Represent OmniaBio and promote its mission and capabilities to the cell and gene therapy field through participation at conferences, symposia, other venues and customer visits. Requirements:
Bachelor’s degree in science (bioengineering, bioprocess, biotechnology, cell biology, microbiology, etc.). Microbiology background preferred.
6+ years of experience in cell therapy/viral quality department supporting GMP production, or similar within the pharmaceutical, medical technologies, biologics, or similar industries.
Strong understanding of aseptic / sterile environment and technologies.
Excellent understanding of Health Canada/US Food and Drug Administration Good Manufacturing Practices (GMP) regulations and QA principles.
Ability to meet Visual Exam Requirements

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 the ability to multitask and succeed in a team environment.
Experience establishing customer-facing organizations and service models.
Demonstrate initiative and the ability to deliver high quality outcomes in dynamic siutations.

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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Refine Your Search

biotechnology jobs in hamilton on

OmniaBio: Microbiologist

QC Analyst

Analytical Development Chemist

Sr. Embryologist

Healthcare CANADA Quality Assurance & Regulatory Affairs Senior Director

Sourcing Specialist

Trial Delivery Management (Advanced)

Enterprise Architect (Business Technology Architect) - Life Sciences

Account Manager

Associate Director, Clinical Operations (Study Startup)

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