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 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.

Job Description

Join Our Team and Help Shape the Future of Biologics!

Are you passionate about advancing innovative biologic therapies? Do you thrive in a dynamic environment where scientific rigor, collaboration, and problem‑solving are at the forefront?
We're looking for an Analyst II, Analytical Development to support technology transfer, method development, qualification, and validation activities within our growing biopharmaceutical analytics group.

The Analyst II, Analytical Development, is accountable for supporting technology transfer, method development, qualification, and validation of analytical methods for the characterization and analytical testing of biologics. The successful candidate will play a key role in planning and executing experimental work to generate data and prepare technical reports for early-stage research, preclinical development, or late-stage CMC programs across various drug modalities.

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 novel 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 Will Achieve in This Role

In this position, you will:

• Become a key contributor to analytical strategies supporting cutting-edge biologic programs.
• Build deep expertise in method development, validation, and the analytical characterization of complex molecules.
• Lead analytical activities that directly inform decisions in process development, regulatory submissions, and tech transfers.
• Strengthen cross-functional collaboration by working closely with QC, Formulations, Process Development, and external partners.
• Help shape best practices, drive continuous improvement, and influence the evolution of Analytical Development capabilities within the organization.
• Advance your career through hands-on technical challenge, exposure to diverse modalities, and mentorship opportunities.

This role is perfect for someone who wants to see their work make a measurable impact across the full lifecycle of biologic development.

Core Responsibilities

• Apply a strong understanding of analytical methodologies to support the testing and characterization of biopharmaceuticals, including monoclonal antibodies, ADCs, fusion proteins, and recombinant proteins.
• Lead and execute analytical method transfers, method development, and validation for drug substance and drug product.
• Plan, conduct, troubleshoot, and document laboratory studies independently while ensuring scientific integrity and quality.
• Clearly communicate data, insights, and recommendations to project teams and larger audiences; contribute to experimental design discussions.
• Develop, optimize, and validate robust analytical separation methods and bioassays to characterize and quantify biologics.
• Collaborate with internal and external partners to support biophysical characterization activities.
• Adhere to GMP and GDP standards in all analytical work.
• Write and review SOPs and work instructions for analytical and lab-related activities.
• Work cross-functionally to drive project timelines and deliverables.
• Contribute to continuous improvement initiatives and provide technical insight to resolve project challenges.
• Mentor junior team members through training, guidance, and feedback.
• Follow EHS guidelines, ensuring safe laboratory operations.
• Support lab operations including equipment maintenance, supply management, and sample shipments.

⭐ Why You'll Be a Great Fit

You will excel in this role if you:

• Bring strong foundational knowledge in analytical characterization of biologics (e.g., mAbs, ADCs, fusion proteins, recombinant proteins).
• Enjoy solving complex scientific problems and designing efficient laboratory strategies.
• Communicate clearly and confidently, both in writing and when presenting data to broader teams.
• Thrive in a fast-paced environment where adaptability, organization, and attention to detail matter.
• Are a collaborative team player who enjoys sharing knowledge, mentoring others, and contributing to a positive lab culture.
• Take pride in high-quality documentation and compliance, understanding the importance of GMP/GDP in biologics development.
• Are proactive, curious, motivated by continuous improvement, and eager to push projects forward.

If you are someone who enjoys taking ownership, driving innovation, and applying critical thinking to real-world therapeutic challenges, you'll feel right at home here.

Videos To Watch