We are seeking an experienced and motivated Scientist II (Separation Science) to join our Analytical Development team. In this role, you will support the development, optimization, and validation of analytical methods used to characterize biologics across R&D, preclinical, and GMP environments. Reporting to the Senior Manager, Analytical Development, you will play a key role in shaping analytical strategy, collaborating across functions, and delivering high鈥憅uality data that enables the successful advancement of diverse biologic programs. This is an excellent opportunity for a scientist who thrives in a dynamic environment, enjoys technical problem鈥憇olving, and wants to contribute meaningfully to innovative therapeutic development.
The Scientist II, Analytical Development, is accountable for supporting technology transfer, method development, qualification, and validation of analytical methods for the characterization, R&D testing, and GMP testing of biologics. The successful candidate will play a key role in planning the analytical strategy and will collaborate with other team members to execute experimental work, generate data, and prepare technical reports for early-stage research, preclinical development, or late-stage CMC programs in support of 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鈥檒l Do
As a Scientist II, you will apply your expertise in separation science and biologics characterization to provide technical leadership and drive analytical excellence:
- Apply strong analytical understanding to support the testing and characterization of biopharmaceuticals, including monoclonal antibodies, ADCs, fusion proteins, and recombinant proteins.
- Serve as a Subject Matter Expert (SME) in analytical development and testing, offering strategic and technical guidance.
- Lead and perform analytical method transfer, method development, and method validation for both drug substances and drug products.
- Independently plan, execute, troubleshoot, and report laboratory work with minimal supervision.
- Clearly communicate results to internal teams and external clients, and actively support the design of subsequent studies.
- Develop, optimize, and validate robust analytical separation methods to quantify and characterize biologics.
- Manage internal collaborations and external partners responsible for biophysical characterization activities.
- Ensure all analytical activities adhere to GMP and GDP standards with strong documentation practices.
- Write, review, and approve SOPs and work instructions related to analytical procedures and laboratory operations.
- Lead or participate in quality event investigations (planned and unplanned), recommending effective corrective and preventive actions.
- Collaborate across multidisciplinary teams to advance projects and provide analytical expertise.
- Drive continuous improvement initiatives and contribute to timely resolution of analytical issues or gaps.
- Train, mentor, and support junior team members through knowledge transfer, hands鈥憃n training, and clear guidance.
- Support daily laboratory operations, including equipment maintenance, supply ordering, and coordinating shipments of materials or samples.
Why Work Here
Joining our team means becoming part of a collaborative, science鈥慸riven environment where your expertise truly makes an impact. Here鈥檚 what you can expect:
- High鈥慽mpact work: Your analyses directly influence decision鈥憁aking across early research, development, and CMC stages.
- Meaningful scientific contribution: You鈥檒l work on diverse biologic modalities and cutting鈥慹dge technologies.
- Growth and development: Exposure to a wide range of analytical techniques, mentorship opportunities, and cross鈥慺unctional project involvement.
- Supportive team culture: Work alongside skilled scientists who value collaboration, learning, and continuous improvement.
- Autonomy and ownership: You will have the freedom to lead methods, drive investigations, and shape analytical strategy.
- Commitment to quality: A strong GMP environment where scientific excellence and compliance go hand in hand.