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

Job Description

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.

Qualifications

• BSc in Biotechnology (or similar field) with up to one (1) year of relevant industry experience is preferred.
• Demonstrated experience in upstream bioprocessing is an asset.
• Experience in SOP drafting and previous involvement in GMP runs is an asset.
• Strong interpersonal skills and ability to work collaboratively as a member of a cross-functional team.
• Excellent communication, GMP documentation, and organizational skills.
• Strong problem-solving skills with the ability to work under minimal supervision.
• Strong interpersonal skills and ability to work collaboratively as a member of a cross-functional team.

The starting annual base compensation for this position is $65,000 CAD. The actual offer, reflecting the total compensation package plus benefits, will be determined by a number of factors which include but are not limited to the applicant’s experience, knowledge, skills, and abilities.

Disclaimer: Salary information posted on sites other than the official careers page does not reflect the organization’s compensation and may represent estimated ranges provided by third-party job boards. The organization offers competitive wages and a comprehensive total rewards package, which will be discussed during the interview process.

At Eurofins CDMO Alphora, we leverage artificial intelligence (AI) technology to support our recruitment process, including preliminary screening of applications and resumes. All hiring decisions are made by human reviewers.

This posting is for a current vacancy and the successful candidate will start as soon as possible.

Additional Information

At Eurofins we offer excellent full-time benefits including health & dental coverage, life and disability insurance, RRSP with 3% company match, paid holidays, paid time off.

Accommodation: Persons with disabilities who need accommodation in the application process, or those needing job postings in an alternative format, may e-mail a request via the website at .

As a Eurofins employee, you will become part of a company that has received international recognition as a great place to work. To learn more about Eurofins, please explore our website at

We thank all applicants within commuting distance of GTA, Ontario for showing an interest in this position. Only those selected for an interview will be contacted.

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