Operations Associate I (Contract)

at  Centre for Commercialization of Regenerative Medicine

ABOUT CCRM:

CCRM, based in Toronto, Canada, is a public-private partnership that is developing and commercializing cell and gene therapies and regenerative medicine-based technologies. We are leveraging our network of academics, industry partners and investors to tackle significant industry challenges and advance our most promising technologies to the market to meet the needs of patients. For more information about CCRM, please visit our website at ccrm.ca.
This is a contract role.
Department: Deliver

POSITION SUMMARY:

As an Operations Associate I at CCRM, you will be part of a diverse bioengineering team focused on designing and implementing good manufacturing practices (GMP) production projects for CCRM’s GMP facility. You will provide technical expertise and will work with the team to define and execute project tasks. You will be an operations leader in bringing new and innovative products to market to enable life-saving advances in cell and gene therapy and regenerative medicine.

QUALIFICATIONS:

• BSc in Biological or Life Sciences, Biotechnology or Microbiology or equivalent industry experience.
• 1+ years of experience in biopharmaceutical based GMP manufacturing operations/Cell Therapy/Human Cell Cultivation.
• Hands-on experience working in a cGMP environment preferred
• Strong English written and verbal communication skills.
• Proven track record of writing GMP documents (i.e., SOPs, validation procedures).

• This position will have responsibilities in CCRM’s GMP facilities.
• Extract information from equipment manuals and other source documents, and write easy-to-understand, simple, user-friendly standard operating procedures (SOPs) that describe the equipment, key operating parameters, maintenance, and cleaning procedures.
• Responsible for cleaning, maintenance, and documentation of equipment in the cleanroom for use.
• Responsible to perform process validation, process optimization and process development as required.
• Responsible to assist in the design/execution of the production batch records or other high-
• quality documents (i.e., HVAC validation) that meet applicable standards and are appropriate for the intended audience.
• Responsible to ensure that the controlled Grade A and B manufacturing areas are clean and remain in a state of control.
• Support the development and execution of appropriate Safety, Training, Gowning, Material Movement, Cleaning, and Scheduling.
• Complete Batch Records (BRs), Logbooks, Forms, etc. under cGMP, and documents in detail through the use of SOPs and BRs for the processes and manufacturing steps
• Responsible to write and update standard operating procedures and master batch records.
• Adhere to GMPs and GDPs (good documentation practices).
• Operate pilot-scale bioprocessing and interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Quality Assurance and Logistical counterparts.
• Collaborate with the Process Development and Manufacturing Sciences and Technology group to transfer new projects into GMP
• Implement a program to monitor and control operations from an employee safety perspective.
• Other process related tasks that may arise.