Job 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 decentralised 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 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Eurofins CDMO Alphora Inc. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients -“API’s”) as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its state-of-the-art organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths.

We are seeking a motivated and technically driven Scientist I, Downstream Process Development to join our growing Process Development team. In this role, you will contribute to the design and optimization of purification and bioconjugation processes for a wide variety of therapeutic proteins and novel biologics.

Working closely with senior scientists and cross‑functional partners, you will support key laboratory studies involving chromatography, tangential flow filtration (TFF), filtration, and nanofiltration, while also helping scale processes toward larger‑volume operations. This is an exceptional opportunity for someone early in their career who is passionate about bioprocessing, enjoys hands‑on lab work, and wants to play a direct role in advancing innovative therapeutics from concept to clinic.

The Scientist I - Downstream Process Development, is involved in the development of novel biologics and therapeutics by assuming a crucial role in the design of purification and bioconjugation processes for a wide range of proteins. The successful candidate will play a key role in laboratory studies for the development of a range of downstream processing steps including chromatography, tangential flow filtration (TFF), filtration, and nanofiltration amongst other steps while being able to communicate progress to internal stakeholders. The ideal candidate will also play key roles in scaling up processes.

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 Do

As a Scientist I, you will be a key contributor to downstream development activities and process innovation:

• Serve as a Subject Matter Expert (SME) in downstream processing principles and best practices.
• Apply bioprocess engineering and protein chemistry knowledge to design and optimize chromatography, TFF, and filtration studies.
• Contribute to the design and execution of protein bioconjugation development activities.
• Draft and review technical documents, including batch records, experimental procedures, data summaries, and scientific reports.
• Communicate research findings clearly and confidently to internal teams and project stakeholders.
• Support continuous improvement initiatives to deliver robust, scalable, and cost‑effective downstream processes for clients.
• Perform hands‑on laboratory execution of planned studies, from buffer preparation to purification runs.
• Record raw data in accordance with GDP/GLP standards, analyze results, and help refine experimental designs.
• Write and review SOPs related to downstream process equipment, unit operations, and batch record documentation, following industry guidelines (GMP, HSE, IP).
• Collaborate across functional teams—including analytical, upstream, engineering, and quality—to advance projects and support equipment qualification activities.
• Independently plan, troubleshoot, and report on laboratory work with minimal supervision.
• Assist in maintaining a well‑run laboratory by performing basic equipment upkeep and ordering consumables.

Why Work Here

Joining our team gives you the chance to grow, contribute, and make a real impact in the development of life‑changing biologics:

⭐ Meaningful Scientific Impact

Your work directly contributes to developing purification strategies and bioconjugation workflows that enable innovative therapeutics.

⭐ Hands‑On Technical Growth

You’ll gain experience with industry‑relevant downstream technologies—including chromatography systems, TFF skids, and advanced filtration techniques.

⭐ A Collaborative, Mentorship‑Driven Environment

Work closely with experienced scientists who are invested in your development and ready to support your learning journey.

⭐ Ownership & Independence

You’ll have the opportunity to plan and execute your own experiments, troubleshoot challenges, and help shape downstream development strategies.

⭐ A Culture of Innovation & Continuous Improvement

We value curiosity, new ideas, and scientific rigor—and we empower you to apply them.

⭐ Career Path for Advancement

This role is designed to support your growth toward Scientist II and beyond, with exposure to scale‑up, tech transfer, and cross‑functional operations.

Qualifications

• Minimum Master’s degree with 3+ years of experience or PhD
• Working knowledge of protein chemistry and protein purification along with self-directed learning and a willingness to grow one’s knowledge.
• Experience with development and execution of chromatography process steps using UNICORN control software.
• Experience with carrying out ultrafiltration and diafiltration studies using TFF.
• Experience in and understanding of aseptic techniques in laboratory setting.
• Knowledge in bioprocess engineering principles underlying effective scale-up design.
• Knowledge of filtration and clarification steps in development and optimization.
• Knowledge of protein bioconjugation (this would be considered an asset).
• Understanding of how to implement Design of Experiments (DoE) and Quality by Design (QbD) in the development of unit operations.
• Understanding of Current Good Manufacturing Practices (cGMP) in biomanufacturing.
• Being a key point of contact and Subject Matter Expert (SME) for scientific studies in the PD lab, communicating scientific information succinctly to a range of audiences.
• 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.

The starting annual base compensation for this position is $80,000 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 www.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 at www.eurofins.ca

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.

NO AGENCIES, CALLS OR EMAILS PLEASE