Job DescriptionKickstart Your Biologics Career. Grow Your Skills. Make an Impact in GMP Manufacturing.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 prospect for someone who is passionate about cell culture, eager to learn, and excited to work in a dynamic, fast‑paced biologics environment.What You’ll Be DoingReporting 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 OperationsAssist 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 SupportSupport 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 ReadinessClean 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 CoordinationAssist with ordering consumables and equipment needed for PD and GMP operations.Support equipment and room qualification activities.Scientific GrowthApply 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 YouYou 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.QualificationsBSc 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.SalaryThe 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.Additional InformationAt 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 www.Eurofins.Ca.#J-18808-Ljbffr

📌 Technologist I, Upstream Manufacturing - Biologics - Eurofins Cdmo Alphora, Inc. - C$65,000 A Year (Winnipeg)
🏢 Eurofins CDMO Alphora
📍 Winnipeg