Scientist I: Bioconjugation - Discovery Sciences

iQ BiosciencesAlameda, CA
Onsite

About The Position

The Scientist I – Bioconjugation is a hands-on scientist responsible for the execution, analysis, and scientific support of bioconjugation studies across client-sponsored and internal research projects. Working closely as the technical lead with Project Management and cross-functional scientific teams, the Scientist I will independently execute complex laboratory workflows, interpret experimental data, troubleshoot moderately complex technical issues, and contribute to experimental design and study planning. The Scientist I is expected to apply sound scientific judgment to assigned work, independently plan routine experiments and optimization activities, adapt established methods to project-specific variables, and recommend appropriate next steps based on experimental results. More complex study design, novel method development, and higher-risk scientific decisions are generally made in consultation with more senior scientific staff. This is a highly hands-on laboratory role suited to a scientist who is ready to move beyond technical execution and take increasing ownership of experimental reasoning, study outcomes, and scientific communication.

Requirements

  • Ph.D. with approximately 0–2 years of relevant post-degree experience; or M.S. with approximately 3+ years of relevant experience; or B.S. with approximately 5–6+ years of progressively responsible relevant experience.
  • Degree in Chemistry, Biochemistry, Chemical Biology, Pharmaceutical Sciences, or a related scientific discipline.
  • Demonstrated experience independently executing, troubleshooting, and interpreting complex laboratory experiments.
  • Industry experience in biotechnology, pharmaceutical, CRO, or a similarly deadline-driven research environment preferred.
  • Hands-on experience with antibody/protein bioconjugation, protein modification, or closely related laboratory workflows.
  • Experience with conjugation chemistries such as maleimide, NHS ester, or comparable approaches.
  • Familiarity with lysine- and cysteine-based conjugation and an understanding of how conjugation chemistry and site may affect distribution, homogeneity, and downstream performance.
  • Strong protein-handling fundamentals, including concentration measurement and careful handling of limited or valuable biological material.
  • Experience with one or more conjugate-characterization methods such as SEC, HIC, UV-Vis, SDS-PAGE, HPLC, or related techniques.
  • Working knowledge of purification principles and chromatography; AKTA/FPLC experience preferred.
  • Demonstrated ability to interpret data, troubleshoot experiments, maintain strong laboratory records, and manage multiple assignments.
  • Competency with data-analysis tools such as GraphPad Prism and Excel.
  • Strong written and verbal scientific communication skills.

Nice To Haves

  • Direct experience with ADCs or other antibody/protein conjugates.
  • Familiarity with DAR measurement and linker-payload chemistry.
  • Exposure to site-specific conjugation approaches.
  • Experience with AKTA or FPLC systems.
  • Experience adapting or optimizing established conjugation, purification, or analytical methods.
  • Experience with multiple antibody isotypes or diverse protein formats.
  • Experience in a CRO or client-service research environment managing concurrent assignments.
  • Experience with LIMS, electronic laboratory notebooks, or project-management systems such as Zoho.
  • Experience providing technical guidance or training to junior laboratory staff.
  • Experience with sterile technique or mammalian cell culture is a plus.

Responsibilities

  • Independently execute antibody and protein bioconjugation reactions using established chemical and/or enzymatic approaches, including maleimide-, NHS ester-, and comparable protein-modification chemistries.
  • Perform purification and buffer-exchange workflows using techniques such as desalting, tangential flow filtration, size-exclusion chromatography, Protein A, and AKTA/FPLC-based systems.
  • Characterize conjugates using analytical methods such as SEC, HIC, UV-Vis, SDS-PAGE, concentration assays, and other appropriate methods; mass spectrometry experience is a plus.
  • Independently execute complex established workflows and adapt experimental execution based on project-specific variables and approved scientific rationale.
  • Plan and perform routine pilot, comparison, optimization, and confirmation experiments.
  • Apply working knowledge of protein chemistry, buffer composition, pH, protein handling, and storage conditions to maintain sample quality and identify potential technical risks.
  • Work carefully and economically with limited, high-value, or client-provided biological materials.
  • Maintain complete, accurate, and timely experimental records and study documentation.
  • Contribute to study design and independently plan routine experiments within defined project objectives.
  • Identify important experimental variables and recommend focused experiments to evaluate routine technical questions.
  • Adapt established conjugation, purification, or analytical methods based on project variables, prior experience, and experimental results.
  • Develop scientific rationale for routine experimental decisions and communicate that rationale clearly to the technical lead and project team.
  • Evaluate whether experimental results adequately address the immediate study question and recommend reasonable follow-up work.
  • Review relevant scientific literature and technical references to inform experimental planning and troubleshooting.
  • Recognize when an experimental question or proposed approach exceeds the scope of routine decision-making and seek appropriate scientific review.
  • Independently troubleshoot moderately complex conjugation, purification, and analytical issues using scientific principles and prior experience.
  • Develop reasonable hypotheses for unexpected results and recommend appropriate follow-up experiments or method adjustments.
  • Perform root-cause analysis for routine or moderately complex experimental problems and escalate novel, high-risk, or broader scientific issues as appropriate.
  • Analyze experimental data using tools such as GraphPad Prism, Excel, or comparable software.
  • Interpret data in the context of study objectives, experimental conditions, and known technical limitations.
  • Identify trends, inconsistencies, deviations, and potential sources of experimental variability.
  • Draw scientific conclusions from assigned work and recommend next steps with appropriate review.
  • Clearly communicate experimental limitations, uncertainties, and technical risks.
  • Take ownership of routine studies or defined scientific components of larger client projects.
  • Coordinate experimental activities and sequencing for assigned work to support project timelines.
  • Manage multiple concurrent studies or workstreams while maintaining accuracy, documentation quality, and responsiveness.
  • Work closely with Project Management to communicate progress, scientific risks, material needs, and potential timeline impacts.
  • Track assigned study activities and proactively identify issues that could affect project execution.
  • Coordinate supporting experimental work performed by Research Associates when appropriate.
  • Ensure assigned experimental work is completed according to iQ scientific and quality expectations.
  • Communicate experimental plans, rationale, results, and recommended next steps clearly to the technical lead, Project Management, and internal scientific teams.
  • Prepare study summaries, figures, tables, reports, and other client deliverables.
  • Participate in technical discussions, data-review meetings, and internal project meetings.
  • Participate in client-facing technical updates or data-review discussions as appropriate to study needs and experience.
  • Answer routine technical questions related to assigned work and escalate significant scientific or strategic issues when appropriate.
  • Surface technical issues, blockers, uncertainties, or changes in project timing promptly.
  • Collaborate effectively with other scientific, project management, laboratory operations, and commercial team members.
  • Adapt and improve established bioconjugation, purification, and analytical methods based on experimental observations and project needs.
  • Contribute to method optimization, transfer, and standardization activities.
  • Draft and revise methods, SOPs, and technical procedures.
  • Identify opportunities to improve reproducibility, efficiency, material utilization, and laboratory workflow.
  • Support evaluation of new reagents, techniques, or equipment relevant to assigned work.
  • Stay current with developments in bioconjugation, ADC technologies, protein chemistry, and analytical characterization.
  • Contribute technical knowledge to internal R&D and capability-development projects.
  • Provide technical guidance to Research Associates working on related studies.
  • Train team members on established methods, laboratory techniques, and equipment when qualified to do so.
  • Review experimental observations or data with junior team members and help reinforce sound technical practices.
  • Contribute to internal scientific discussions and knowledge-sharing.
  • Serve as a reliable technical resource within assigned areas of expertise.

Benefits

  • Medical
  • dental
  • vision
  • 401(k) with employer match after the introductory period
  • paid holidays
  • paid time off
  • EAP
  • life and long-term disability insurance
  • FSA with employer contribution
  • company-provided lunch and snacks
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