$93,673–$112,950 Per Year
Analysis Skills, Antibodies, Assay Development, Assays, Biology, Biotech and Pharmaceutical, Cancer, Clinical Research, Clinical Validation, Cross-Functional, Detail Oriented, Disease, Document Management, Documentation, Experiment Design, IP (Internet Protocol), Identify Issues, Laboratory, Laboratory Information Management System (LIMS), Laboratory Notebook, Leadership, Manufacturing/Industrial Processes, Medicine, Microscopy, Microsoft Excel, Microsoft PowerPoint, Microsoft Word, Molecular Biology, Patents, Phlebotomy, Prism, Product Development, Product Lifecycle, Project Planning, Protein Purification, Quality Control, Real-time PCR (qPCR), Record Keeping, Root Cause Analysis, Spectroscopy, United States Department of Energy (DOE), Writing Skills
Scientist, Development - Mercy BioAnalytics
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Scientist, Development
Mercy BioAnalytics, Inc., is a biotechnology company dedicated to reducing suffering and saving lives through the early detection of cancer. Backed by extensive clinical validation, we are advancing one of the most important innovations in modern medicine: detecting cancer at its earliest, most treatable stages through a simple blood draw.
We are looking for a passionate and experienced Scientist to join our Early Development team. The successful candidate will design, execute, and analyze experiments related to assay optimization, analyte and reagent characterization, and novel assay development. In addition, this role will also contribute to Mercy's IP portfolio through innovative and creative thinking and experimentation. This role is ideal for an expert in characterization, validation, and troubleshooting, with a deep understanding of antibody-based detection systems and a proven track record of developing high-performance assays for research or clinical use for the early detection of disease.
Candidates for this position must enjoy working for a fast-paced, cutting-edge company and demonstrate exemplary situational leadership capabilities and a passion for contributing to our life-saving mission.
Responsibilities:
- Responsible for reagent development within a design-controlled organization
- Responsible for drafting and managing documentation associated with the production and characterization of reagents
- Independently design and execute reagent characterization and qualification experiments for improved assay function, robustness, and QC method development
- Lead and execute design of experiments (DOE) for reference material and reagent optimization and guard-banding
- Accountable for data and root cause analysis during product development lifecycle
- Establish project plans to meet milestones based on company goals
- Author design-controlled documentation during product development
- Work as a key member within a cross functional team to identify improved methods, workflows, and reagent manufacturing processes
- Maintain accurate records of experiments in line with quality requirements
- Collaborate and communicate within a matrixed cross functional environment including status updates to broader team
- Present data at external scientific meetings, proactively publish and patent
Requirements:
- BSc/MS life science degree + 5 years' industry experience or a PhD.
- Minimum 3+ years of laboratory experience in assay or product development in a biotech or pharma setting is required.
- Experience with mammalian tissue culture is required
- Proficiency with standard bioanalytical and molecular biology techniques including Flow Cytometry, ELISA, qPCR, absorbance spectroscopy, pH and conductivity.
- Previous experience purifying extracellular vesicles, knowledge of protein purification techniques and novel high-resolution microscopy methods is preferred.
- Previous experience with protein bioconjugation techniques and familiarity with bioconjugate purification methods is strongly preferred.
- The ability to follow established controlled documentation with strict attention to detail.
- Proficiency in collecting and accurately documenting experimental procedures and results is essential. Familiarity with electronic lab notebook (ELN) or laboratory information management systems (LIMS) is strongly preferred.
- The ability to work effectively and efficiently with other team members in a fast-paced and dynamic environment is essential.
- Proficiency in software applications like PRISM, Microsoft Word, Excel, and PowerPoint is required.
- Ability to work in a fast-paced environment and adapt to changing priorities
Hiring Manager: Sr. Director, Development
Location: In Person - Waltham, MA
Status: Full-Time
JOB ID: DEV011
Base Salary Range: $93,673 - $112,950
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