Current jobs related to Quality Control Associate I - Toronto - CCRM
-
Quality Control Associate I, Reagents
4 months ago
Toronto, Canada DiaSorin Full time**Job Title**: Quality Control Associate I, Reagents - Toronto JOB SUMMARY - Executing core Quality Control (QC) processes associated with reagent consumable and bioassay production, reagent stability program, and controlled storage monitoring. - Assisting with incoming quality control, departmental calibration and maintenance and the retention program. -...
-
Quality Control Associate I, Reagents
3 months ago
Toronto, Canada DiaSorin Full timeDiasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the...
-
Quality Control Associate
2 weeks ago
Toronto, Canada Pharma Medica Research Inc. Full timePharma Medica Research is a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special and patient populations. We're currently searching for a Clinical QC Associate I to join our growing team!The function of the Clinical QC Associate I is to ensure all prepared study source documents...
-
Quality Control Associate Ii
3 months ago
Toronto, Canada Centre for Commercialization of Regenerative Medicine Full time**About CCRM**: Deliver - GMP Contract Manufacturing - Quality Control Associate II **Position Summary**: As a Quality Control Associate II at CCRM, you will be part of a diverse bioengineering team focused on designing and implementing a quality management program within the cell and gene therapy and regenerative medicine fields. You will provide technical...
-
Project Control Officer
2 weeks ago
Old Toronto, Ontario, Canada S I Systems Full timeProject Control Officer - Banking**Job Summary**S I Systems is seeking a highly skilled Project Control Officer to join our team. As a Project Control Officer, you will be responsible for ensuring the successful delivery of projects within the Banking sector.**Key Responsibilities**Maintain accurate and up-to-date project budgets, including auditing and...
-
Project Control Officer
2 weeks ago
Old Toronto, Ontario, Canada S I Systems Full timeProject Control Officer - Banking**Job Summary**S I Systems is seeking a highly skilled Project Control Officer to join our team. As a Project Control Officer, you will be responsible for ensuring the successful delivery of projects within the Banking sector.**Key Responsibilities**Maintain accurate and up-to-date project budgets, including auditing and...
-
Pharmacovigilance Associate I
2 weeks ago
Toronto, Ontario, Canada CB Canada Full timeAbout the RoleWe are seeking a highly motivated and detail-oriented Pharmacovigilance Associate I to join our team at CB Canada. As a key member of our Pharmacovigilance department, you will play a critical role in ensuring the safety and efficacy of our pharmaceutical products.Key ResponsibilitiesInformation Management: Receive, scan, and document all...
-
Pharmacovigilance Associate I
2 weeks ago
Toronto, Ontario, Canada CB Canada Full timeAbout the RoleWe are seeking a highly motivated and detail-oriented Pharmacovigilance Associate I to join our team at CB Canada. As a key member of our Pharmacovigilance department, you will play a critical role in ensuring the safety and efficacy of our pharmaceutical products.Key ResponsibilitiesInformation Management: Receive, scan, and document all...
-
Quality Control Associate
4 months ago
Toronto, Canada Printful Full timePrintful is an on-demand printing and fulfillment company that helps people turn their ideas into brands and products. We fulfill and ship custom clothing, accessories, and home & living items for online businesses. Since its founding in 2013, Printful has scaled to a vast team of experts across fulfillment centers worldwide and has become the first company...
-
Pharmacovigilance Associate I
2 weeks ago
Toronto, Ontario, Canada CB Canada Full timeAbout the RoleWe are seeking a highly skilled and detail-oriented Pharmacovigilance Associate I to join our team at CB Canada. As a key member of our Pharmacovigilance department, you will play a critical role in ensuring the safety and efficacy of our pharmaceutical products.Key ResponsibilitiesInformation Management and Pharmacovigilance: Receive, scan,...
-
Pharmacovigilance Associate I
2 weeks ago
Toronto, Ontario, Canada CB Canada Full timeAbout the RoleWe are seeking a highly skilled and detail-oriented Pharmacovigilance Associate I to join our team at CB Canada. As a key member of our Pharmacovigilance department, you will play a critical role in ensuring the safety and efficacy of our pharmaceutical products.Key ResponsibilitiesInformation Management and Pharmacovigilance: Receive, scan,...
-
Quality Control/ Quality Assurance Associate
4 months ago
Toronto, Canada Thornhill Medical Full timeABOUT THORNHILL MEDICAL:Thornhill Medical’s ground-breaking products are designed to be used globally by emergency health care providers, humanitarian, and military medical teams. Thornhill’s oxygen-focused research and applications are transforming patient care in extreme circumstances, while inspiring and enabling other new technologies to unlock vital...
-
Quality Inspectors
4 months ago
Toronto, Canada TRIGO Global Quality Solutions Full timeQuality Inspectors Paid Sick Days, Safety Wear Allowance, Paid OT after 40 hrs. worked in a week, Referral Bonuses and Shift Premium (aft and night shifts), (all offered after meeting the eligibility requirements). We also offer Employee Perks and Discounts, Advancement Opportunities and Travel Opportunities, Flexible hours and more!TRIGO has several...
-
Compliance Associate I
3 months ago
Toronto, Canada Centre for Commercialization of Regenerative Medicine Full time**About CCRM**: As a Compliance Associate I at CCRM, you will be part of the field of Good Manufacturing Practices (GMP) in the manufacturing of regulated products and driven by the opportunity to enable clinical translation of cell and gene therapies. You will help support CCRM’s Quality Assurance and Quality Control teams to deliver on client demands,...
-
Infection Control Practitioner I
3 weeks ago
Toronto, Ontario, Canada University Health Network Full timeJob Title: Infection Control Practitioner I Company: University Health Network (UHN) UHN is a leading research teaching hospital, bringing together over 16,000 employees, more than 1,200 physicians, 8,000+ students, and many volunteers. Our mission is to transform lives and communities through excellence in care, discovery, and learning. Job Description This...
-
Scientific Associate I
4 months ago
Toronto, Canada University Health Network Full time**Position: Scientific Associate I** **Location: MaRS Centre, Toronto** **Department: PanCuRx** **Reports To: Director, PanCuRx** **Salary: Commensurate with level of experience** **Hours: 35 hours/week** **Job Type: Hybrid** **Status: Full-Time, Permanent** The Ontario Institute for Cancer Research (OICR) is seeking a Scientific Associate I to join the...
-
Research Associate I
2 weeks ago
Toronto, Ontario, Canada University Health Network Full timeJob Title: Research Associate IAt the University Health Network, we are seeking a highly skilled Research Associate I to join our team in the Princess Margaret Genomics Centre. As a key member of our research team, you will be responsible for managing projects, coordinating collaborations, and ensuring the successful execution of grant-funded activities.Key...
-
Research Associate I
2 weeks ago
Toronto, Ontario, Canada University Health Network Full timeJob Title: Research Associate IAt the University Health Network, we are seeking a highly skilled Research Associate I to join our team in the Princess Margaret Genomics Centre. As a key member of our research team, you will be responsible for managing projects, coordinating collaborations, and ensuring the successful execution of grant-funded activities.Key...
-
Toronto, Ontario, Canada Control Risks Full timeJob Title: Associate Director of Project Management ServicesWe are seeking a highly skilled and experienced Associate Director to join our team at Control Risks. As a key member of our leadership, you will be responsible for managing and executing complex investigative projects, leading a team of researchers, and developing business development...
-
Toronto, Ontario, Canada Control Risks Full timeJob Title: Associate Director of Project Management ServicesWe are seeking a highly skilled and experienced Associate Director to join our team at Control Risks. As a key member of our leadership, you will be responsible for managing and executing complex investigative projects, leading a team of researchers, and developing business development...
Quality Control Associate I
3 months ago
**Position Summary**:
As a Quality Control Associate I (Microbiology) at CCRM, you will be part of a diverse bioengineering team focused on designing and implementing a quality management program within the cell and gene therapy and regenerative medicine fields. You will provide technical expertise and will work within the team to define and execute project tasks, as well as day-to-day operational duties. You will be a Quality Control (QC) team member who helps to bring new and innovative products to market to enable life-saving advances in cell and gene therapy and regenerative medicine. As a QC Microbiology team member, you will be responsible for an environmental monitoring (EM) program in the facility, as well as QC testing for batch release.
**Responsibilities**:
- Maintains a level of expertise in the QC Microbiology team regarding equipment and operations to support manufacturing for CCRM and its clients.
- Provides technical support to help create and revise an aseptic strategy policy for manufacturing to implement in the Centre for Cell and Vector Production (CCVP) and all CCRM-managed sites.
- Designs, organizes and maintains the standard operating procedures (SOPs) that describe equipment’s key functions including, but not limited to, the operations and maintenance procedures.
- Provides recommendations in the areas of microbiology, aseptic processing and contamination control program and mitigation planning.
- Analyzes existing EM and other QC-related SOPs for content.
- Conducts EM to support current and future operations.
- Maintains documentation for the EM program and studies data trending for the facility, at regular intervals. Plans corrective action if any deviation is observed.
- Facilitates the training of end-users on EM sampling requirements, sample handling and other quality procedures, if applicable.
- Creates equipment log books/records and a preventative maintenance schedule for applicable equipment.
- Maintains equipment, monitors process areas and ensures they are prepared for use.
- Supports the monitoring of deviations for the manufacturing facilities and, if they are above alert/action limit, liaises with other departments for timely resolution.
- Supports third-party testing by our approved partners.
- Performs aseptic gowning qualification and maintains personnel qualifications.
- Performs QC microbiology testing and supports any outsourced testing for lot release/stability studies.
- Conducts troubleshooting when testing failures occur.
- Writes protocols, tests, methods and technical reports, as required.
- Responsible for other process-related tasks that may arise.
- Enforces Good Manufacturing Practices (GMP) in everyday tasks.
- Demonstrates CCRM’s values of purpose, integrity, excellence, accountability and collaboration, and motivates others to do the same.
- Continuously grows and adapts in a fast-moving industry to keep yourself and the organization at the forefront of the cell and gene therapy and regenerative medicine fields.
**Requirements**:
- Bachelor of Science degree in microbiology or biology preferred.
- 1-3 years previous related experience in a GMP environment.
- Strong presentation skills and English written and oral communication skills.
**Desired Characteristics**:
- Understands Health Canada/U.S. Food and Drug Administration GMP regulations and quality assurance principles.
- Proven experience writing GMP documents (i.e. SOPs, validation procedures).
- Able to deliver high-quality work with attention to detail.
- Able to quickly grasp complex technical concepts and make them easily understandable in text and pictures.
- Excellent communication and interpersonal skills with assertive, responsible and accountable attitude.
- Strong working knowledge of Microsoft Office.
- Basic familiarity with an electronic quality management system, laboratory information management system and manufacturing execution systems.
Revision Number**: CCRMQCAIMB-20240613
