Eurofins CDMO Alphora Inc. is a leading contract development and manufacturing organization specializing in complex active pharmaceutical ingredients (APIs). We are looking for a driven Process Specialist to join our Technology Transfer team and play a key role in bringing innovative chemical processes from development to full-scale GMP manufacturing. This is an exciting opportunity for an early-career professional who is passionate about pharmaceutical manufacturing, thrives in a fast-paced technical workplace, and loves collaborating across diverse scientific and operational teams. About the Role As a Process Specialist, you will serve as a critical bridge between our R&D; teams, Operations, and our clients. Working under the guidance of senior team members, you will help design, implement, and support safe, scalable, and compliant manufacturing processes within our cGMP facilities. This client-facing, cross-functional role offers hands‑on exposure to every stage of the manufacturing lifecycle—from process design and batch record generation to on-the-floor support and production troubleshooting. It’s the perfect entry point for someone eager to grow into a technical operations, technology transfer, or manufacturing leadership path. What You’ll Do Be a Key Contributor to Process Scale-Up & Technology Transfer Collaborate with stakeholders across R&D;, QC, QA, Operations, Supply Chain, and Engineering to design safe, scalable processes from gram to multi‑kilogram scale. Support the generation, review, and execution of Master Batch Records (MBRs), Production Batch Records (PBRs), and Executed Batch Records (EBRs). Provide technical support during manufacturing campaigns, spending required time “on the floor” to guide batch execution. Drive Operational Readiness & Project Success Participate in batch scheduling, readiness checks, material availability reviews, and daily Operations activities. Support Material Readiness by coordinating bills of materials (BOMs) and maintaining tracking tools. Contribute to Campaign Summary Reports and process data trending to support continuous improvement. Serve as the Operations Point of Contact Represent Operations in internal and external project meetings. Provide timely production updates to clients and help maintain strong communication throughout each project. Assist in managing process deviations, amendments, SOP updates, and other quality-related activities. Contribute to a Culture of Safety & Compliance Uphold cGMP, Environmental Health & Safety (EHS), Good Documentation Practices, and internal procedures. Ensure accurate,



timely documentation and elevate any incidents or concerns. Participate in On-Call Support (as per rotation) Provide after-hours support to resolve processing issues, report IPCs, and collaborate with QA, R&D;, and Ops leadership when needed. What You Bring A degree in chemistry, chemical engineering, life sciences, or a related discipline. Strong attention to detail and commitment to safety and compliance. Excellent communication and collaboration skills. An eagerness to learn, ask questions, and grow within a high-performing technical environment. A passion for solving problems and supporting complex chemical manufacturing processes. Why Join Eurofins CDMO Alphora? Work at the intersection of science, manufacturing, and client engagement. Gain hands‑on experience with cGMP manufacturing and technical transfer. Collaborate with industry experts and contribute to impactful pharmaceutical projects. Grow your career within the global Eurofins network—home to more than 61,000 employees worldwide. Qualifications: STEAM Degree with preference for BSc/MSc Strong teamwork, communication, and problem‑solving skills Ability to work effectively in a regulated environment 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. WHO ARE WE? Eurofins CDMO Alphora Inc.



provides a fully integrated suite of services to support drug substance and drug product development from the IND enabling development stage, through to phase II & III supply, and commercial validation and manufacturing for niche APIs. In addition to a continuing flow of interesting and challenging projects for global pharmaceutical and biotech companies, Eurofins CDMO Alphora Inc. is committed to growing its state‑of‑the‑art organization, with continued investments in its people, modern facilities, equipment, and instrumentation. COMPANY DESCRIPTION

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralized and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years. 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 atwww.eurofins.ca . 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 atwww.eurofins.ca

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📌 Process Specialist (Technology Transfer) (Winnipeg)
🏢 BioTalent Canada
📍 Winnipeg