Technologist I, Upstream Manufacturing - Biologics - Eurofins CDMO Alphora, Inc.

Kickstart Your Biologics Career. Grow Your Skills. Make an Impact in GMP Manufacturing.

Are you ready to launch your career in biologics while working hands‑on with cutting‑edge upstream technologies? As a Technologist I in Upstream Processing, you’ll play an essential role in supporting GMP manufacturing activities—from preparing and operating bioreactors to maintaining cleanroom readiness and contributing to process development.

This is the perfect opportunity for someone who is passionate about cell culture, eager to learn, and excited to work in a dynamic, fast‑paced biologics environment. You’ll gain exposure to GMP operations, process development, scale‑up, and technology transfer—all while supporting the production of life‑changing therapeutics.

 The Technologist I in the Upstream Processing team is accountable for executing and reporting on upstream Good Manufacturing Practices (GMP) activities, including support with drafting of Bath Production Records (BPRs) and Standard Operating Procedures (SOPs), preparation and staging for cleanroom activities, equipment and room qualification, cell passaging/cultivation, and play a supporting role in the operation of small-to-large-scale bioreactors within the Biologics Business Unit.  In addition to hands-on cleanroom activities, the ideal candidate will be involved in the assisting of technology transfer, process development, scale-up design, and writing of experimental reports.

At Eurofins CDMO Alphora Inc., our mission is to harness the power of biotechnology and bioprocessing to create innovative complex medicines that will improve the lives of patients worldwide. With a dedicated team of experienced scientists, motivated technologists, and state-of-the-art process development (PD) facility, we are thrilled to be at the forefront of the biopharmaceutical CDMO industry in Canada. Join us on this exciting journey as we push the boundaries of scientific research and provide hope to our most vulnerable.

 What You’ll Be Doing

Reporting to the Manager, Upstream Process Development, you will support upstream activities across both PD and GMP manufacturing, contributing to scientific operations, documentation, and day‑to‑day suite readiness.

Hands-On Upstream Operations

• Assist with planning, staging, and executing upstream GMP runs.
• Operate and perform basic maintenance on key upstream equipment including SU bioreactors, shaker incubators, cell counters, peristaltic pumps, and mixers.
• Execute upstream tasks such as vial thaws, seed expansion, media/buffer prep, bioreactor setup, and harvest depth filtration.
• Apply strong aseptic technique during all cleanroom and cell culture activities.

Documentation & Technical Support

• Support drafting of Batch Production Records (BPRs), SOPs, and equipment qualification documents.
• Prepare sample vials and run routine analytical tests (cell counts, metabolite/nutrient analysis, pH/conductivity).
• Document raw data accurately (GDP/GLP) and assist in evaluating results and planning next‑step experiments.
• Participate in writing experimental reports and supporting technology transfer and scale‑up work.

🏭 Cleanroom & GMP Suite Readiness

• Clean GMP cleanrooms and pilot suites as needed.
• Help maintain an always‑inspection‑ready environment for audits and regulatory visits.
• Follow cleanroom PPE requirements and ergonomic best practices when handling equipment or biohazardous materials.
• Maintain manufacturing and PD areas in accordance with CL2 and cGMP standards.

Materials & Equipment Coordination

• Assist with ordering consumables and equipment needed for PD and GMP operations.
• Support equipment and room qualification activities.

Scientific Growth

• Apply foundational knowledge of upstream processing, mammalian cell physiology, and bioprocess engineering.
• Work closely with experienced scientists and engineers to broaden your technical skill set.

Why This Role Is a Great Fit for You

• You want hands‑on experience in cell culture and GMP manufacturing.
• You’re excited to learn bioprocessing fundamentals from experts in the field.
• You’re detail‑oriented, safety‑focused, and eager to contribute to meaningful scientific work.
• You thrive in environments where teamwork, precision, and continuous improvement matter.