Manufacturing Technologist, Upstream
About The Position
The Biologics Manufacturing Center (BMC) Inc. is a new biomanufacturing facility created in response to the pandemic. A not-for-profit organization, the BMC aims to better meet the biopharmaceutical needs of Canadians. The BMC helps support projects of public interest, actively contributes to the overall growth and resilience of the Canadian life sciences industry and fosters industry development and innovation through Canadian production. Backed by a committed and innovative team of employees, the BMC fosters a culture of agility and transparency, with a collaborative, result-oriented approach. We are looking for a Manufacturing Technologist to join our upstream team. At the heart of manufacturing operations, this individual will be part of a small, highly technical team responsible for preparing, executing, and documenting manufacturing activities for biological products and vaccines.
Requirements
- You hold at least a post-secondary diploma in a life sciences-related discipline.
- You have a minimum of three (3) years of experience in preparing, executing, and documenting GMP manufacturing activities in the biopharmaceutical or biotechnology industry.
- You have practical experience with cell culture, aseptic techniques and bioreactor operations.
- The regular schedule is daytime, Monday to Friday; however, based on manufacturing cycles, overtime may be required, including nights, weekends, and holidays.
- You must be able to handle and lift up to 10 kilograms.
Nice To Haves
- A combination of relevant education and experience may be considered.
Responsibilities
- Carry out cell culture activities in a highly regulated environment, strictly adhering to GMP guidelines.
- Operate single-use bioreactors to grow and monitor cells under controlled conditions, including seed culture and inoculum preparation.
- Execute key production steps such as cell expansion and scale-up, virus amplification and infection, as well as harvesting, sampling and primary recovery operations.
- Contribute to data analysis, complete batch record documentation, and support the cleaning and maintenance of the facility.
- Maintain accurate and up-to-date documentation, including technical logs, records and inventories.
- Follow clearly defined processes in compliance with GMP requirements and customer-specific protocols.
- Ensure the safe handling and disposal of single-use bags and biohazardous materials, including those involving pathogenic organisms.
- Support continuous improvement by updating quality documentation, including Standard Operating Procedures (SOPs) and work instructions.
Benefits
- A flexible schedule
- A culture of transparency, notably with our monthly corporate meetings
- A respectful and friendly work environment
- A new building with state-of-the-art equipment
- A competitive salary commensurate with your skills
- An attractive vacation and leave program
- A group RRSP with a generous contribution from the BMC
- A comprehensive insurance plan including telemedicine
- An opportunity to participate in our various life committees (social club, employee committee, OHS committee, etc.)
- A host of activities throughout the year to socialize with your colleagues, recognize team successes and improve your knowledge.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
