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Senior Protein Scientist

Job in Portage, Kalamazoo County, Michigan, 49002, USA
Listing for: Northern Bio
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
  • Research/Development
    Research Scientist, Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

2 days ago Be among the first 25 applicants

Role Summary

Primarily responsible for planning, conducting, and analyzing protein assay method development, qualification, and validation experiments with a specialized focus in Anti-Drug Antibody ADA and pharmacokinetic (PK) bioanalysis
. Uses fundamental concepts, practices, and procedures of protein biology to perform scientific research tasks requiring the application of established bioanalytical techniques, procedures, and criteria. May also act as the Principal Investigator responsible for overall planning and conduct of the study in accordance with applicable regulatory guidelines and contemporary scientific practice.

Must Have Qualifications
  • Strong understanding of biomarker and anti-drug-antibody (ADA) analysis
  • Strong understanding of the FDA ADA guidance for Immunogenicity Testing of Therapeutic Protein Products.
  • Strong understanding of the ICH M10 guideline for bioanalytical method validation and analysis of study samples
Role Responsibilities
  • Ability to develop, optimize, qualify, and validate new ADA assays in both pre‑clinical and clinical laboratory environments.
  • Ability to develop, optimize, qualify, and validate new assays to assess the pharmacokinetics of large‑molecule drug candidates in both pre‑clinical and clinical laboratory environments.
  • The scientist must possess a strong understanding of biomarker and anti‑drug‑antibody (ADA) analysis and be able to execute assays within these areas under the guidance of the Study Director/Principal Investigator, in collaboration with other scientific staff leading the method development and validation procedures.
  • Strong understanding of the FDA ADA guidance for Immunogenicity Testing of Therapeutic Protein Products. Must possess the ability to design assays that meet, or exceed, testing requirements outlined in the available guidance documents and provide scientific justification for deviating from the regulatory testing requirements.
  • Strong understanding of the ICH M10 guideline for bioanalytical method validation and analysis of study samples. Must possess the ability to design assays that meet, or exceed, testing requirements outlined in the available guidance documents and provide scientific justification for deviating from the regulatory testing requirements.
  • Conduct sample analysis of various biological matrices in support of pre‑clinical and clinical studies for ADA, PK, and biomarker assays
  • Lead the department in onboarding new instrumentation and applications. This includes, but is not limited to, developing IQOQ documents and working with IT personnel on Computer System Validation (CSV) script development and execution, while simultaneously implementing SOPs and procedures on operation and maintenance
  • Study monitoring as a lead scientist and data review, as needed. The Senior Scientist is expected to have a full understanding of progress and status of method development and validation studies in their purview and relay this information to management and study directors in a timely and comprehensive manner.
  • Ensures that unforeseen circumstances that may affect the quality and integrity of the laboratory study are noted when they occur, and corrective action is taken and documented.
  • Interfacing with Sponsors, Vendors, Contributing Scientists, and Principal Investigators, as needed.
  • Establish relationships with clients and secure trust through high quality scientific execution, with timely and accurate updates provided through sponsors meetings, method development summaries, and presentations. Responsible for providing scientific guidance and direction during interactions with clients, when necessary.
  • Drive efficiencies through automation/new technologies in assay development, validation, sample preparation, analysis, and reporting
  • Write and review reports, methods, and SOPs
  • Maintain laboratory and freezer inventory, manage instrumentation maintenance and troubleshooting
  • Mentor and guide junior scientists and technicians
  • May serve as the Principal Investigator or Study Director for internal and external studies. Maintains the overall responsibility for the technical conduct of the study,…
Position Requirements
10+ Years work experience
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