Technical lead for development of NGS sample prep and other workflows on Volta’s digital fluidics platform. Volta is building a suite of genomics applications for its disruptive digital fluidics sample prep automation platform.

Author and execute study protocols governing bioanalytical studies to support in vivo studies and sample analysis. In addition: What you will do: The functions of this Scientist position will include bioanalytical/analytical LC-MS sample analysis, LC-MS method development and validation, study design and execution, and data analysis with critical thinking.

Provide technical skills training to the research community in support of IACUC-approved research protocols, e.g. animal handling and restraint, weaning, tail snips, ear tagging, blood and other tissues sample collection, injections, treatments, surgical preparation, pre-, peri-, and post-operative observations, euthanasia, and assists with research procedures as directed.

This role is a commercial and outward facing role and will participate in pre-sales activities including, but not limited to, presentation of the technology and its applications in addition to assay demo through sample testing.

Building off of this core technology, Volta has created a product that streamlines DNA sequencing sample prep. Volta Labs is an MIT spin-off that has unlocked powerful new DNA sequencing capabilities by developing novel fluidic technology.

Experienced in tissue sample processing for molecular biology biomarkers such as DNA, RNA extraction. The Senior Research Associate will be a key player in driving genomic medicine pipeline project through target validation, candidate selection and IND-enabling phases using in vitro, in vivo and ex vivo studies.

Conduct comprehensive training sessions for customers, focusing on microscopy-guided proteomics applications, sample preparation techniques, and image analysis methodologies. Job Summary: As a Field Application Scientist specializing in Advanced Microscopy Applications for Cell and Tissue Biology, you will be at the forefront of translating cutting-edge microscopy technologies into impactful solutions for researchers in life sciences.

Responsibilities: Lead biological projects related to Alzheimer's Disease (AD) through experimental design, sample preparation for mass spectrometry proteomics, and data analysis & interpretation as a subject matter expert.

Interacts on a technical level with CROs in the areas of PK /ADA assay development, with an eye towards validation, and sample processing. A deep understanding of PK and ADA assay development principles and techniques (ELISA, MSD, BLI, SPR, MS, %recovery) with precision and accuracy.

About the Job The Molecular Technologist II position is a key member of the clinical diagnostic laboratory operationsstaff responsible for performing all aspects of complex patient sample testing, solution and reagentpreparation, equipment maintenance and tasks that pertain to the handling and testing of patientspecimens.

Provide ongoing management, education, and support of patients in all phases of treatment including nursing visits; medication management; storage, monitoring, and administering controlled medications; administration and interpretation of urine toxicology screens, integration with primary care and behavioral health, linkage and coordination with external programs, medication teaching, supportive counseling, and medication refills.

However, the applicant will also be responsible for literature reviews, study design, IRB submission, sample testing, medical record reviews, statistical analysis, and manuscript preparation. The clinical laboratory at BWH utilizes innovative technologies and dedicated staff to perform over 7 million tests per year for our patients at BWH and Dana Farber Cancer Institute, both affiliates of Harvard Medical School.

The candidate will work closely with clinical laboratory leadership (Drs. Melanson, Tanasijevic, and Tolan (detailed background and publication history can be found on Harvard Catalyst profiles ) and other clinical colleagues including internal medicine, primary care, nephrology, emergency medicine and palliative care.

As a Metallurgical Engineering Co-Op, you will be responsible for performing materials sample preparation, characterization, and analysis for the Anode Development Team. This role will offer exposure to alloy development, process engineering, and manufacturing of inert anodes to be used in aggressive Metal Oxide Electrolysis (MOE) cell environments.

The Sr Manager, GCP Quality Assurance coordinates GCP Compliance activities with Clinical Operations, Regulatory Affairs, Clinical Supply & Logistics, Sample Management and Pharmacovigilance as well as varied vendors supporting Clinical Studies.