Analyst II, Method Transfer Sciences; Biochemistry
Listed on 2026-10-17
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Research/Development
Biotech Research, Regulatory Compliance Specialist, Pharmaceutical Science/ Research, Research Scientist
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Location:
Winnipeg, MB, CA, R3T 5Y3
Preparedness today, safer tomorrow.
Emergent is a leading public health company that delivers protective and life‑saving solutions to communities around the world. Here, you will join passionate professionals where our culture is informed by our values and commitment to protecting and saving lives.
Job SummaryAnalyst II, Method Transfer Sciences (Biochemistry) serves as a technical resource supporting the transfer, validation, verification, and continuous improvement of analytical and biological test methods within a regulated laboratory environment.
The role supports a range of technologies including mass spectrometry, bioassays, immunological methods, and other analytical platforms while collaborating cross‑functionally to ensure methods are fit for purpose and compliant with regulatory expectations.
ResponsibilitiesReasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions.
- Scientifically and practically evaluate analytical and biological methods, procedural changes, and validation strategies to ensure appropriate methodology is applied.
- Support implementation of new technologies and approaches that improve assay performance, sensitivity, robustness, and efficiency.
- Participate in transfer, verification, validation, and optimization of bioassays and immunological methods.
- Support execution of biological testing techniques including ELISA, ligand‑binding assays, cell‑based assays, flow cytometry, and related immunological methodologies where applicable.
- Interpret complex biological and analytical data and communicate conclusions effectively to stakeholders.
- Lead or independently execute analytical method validations, method improvements, and investigations, ensuring accurate documentation and regulatory compliance.
- Collaborate cross‑functionally to communicate scientific rationale, validation approaches, and data interpretation clearly and effectively.
- Apply advanced knowledge of analytical, biological, and compendial methodologies with a strong understanding of applicable regulatory requirements.
- Contribute technical insight and innovative ideas to troubleshooting efforts and root‑cause investigations.
- Maintain complete, accurate, and contemporaneous laboratory records in accordance with Good Manufacturing Practices (GMP) and internal procedures.
- Have strong communication skills; ability to articulate effectively in both written and verbal forms.
- Have strong organizational and interpersonal skills and the ability to work collaboratively with others.
- Strong leadership capabilities, independence, and initiative.
- Ability to successfully complete a pre‑employment medical assessment.
- Able to work flexible hours or shifts.
- Master's degree in Immunology, Biochemistry, Biology, Biotechnology, Pharmaceutical Sciences, Analytical Chemistry, or a related scientific discipline with relevant laboratory experience.
- Bachelor of Science (BSc) in Immunology, Biology, Biochemistry, Biotechnology, Pharmaceutical Sciences, Chemistry, or related field with a minimum of five (5) years of relevant analytical, bioassay, immunology, or biopharmaceutical laboratory experience
- Demonstrated expertise in analytical and/or biological method validation, method transfer, qualification, and regulated laboratory environments.
- Experience with bioassays, immunological assays, cell‑based methods, or biologics testing is strongly preferred.
- Knowledge of ELISA, MSD, flow cytometry, ligand‑binding assays, cell culture, potency testing, or…
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