87 Results for

Bioanalytical Scientist Jobs in the United States

Jobs

New!

Boston, MAToday

$137,000–$215,270 Per Year

This role contributes to critical function delivery as follows: Accelerates Discovery through Automation and AI-Integrated DMTA: Designs and executes bioanalytical assays in 384- and 1,536-well formats on fully automated, robotic platforms with integrated workflows, enabling rapid, high-throughput testing and iterative optimization. The Senior Scientist will partner closely with DMPK, medicinal chemistry, data sciences, and automation engineering to translate complex bioanalytical data into actionable insights that accelerate portfolio progression and enable data-driven decision-making.

New!

Boston, MAToday

$103,500–$162,690 Per Year

This role contributes to critical function delivery: Accelerates Discovery Through Automation & AI Integration: Implements and operates fully automated, end-to-end assay workflows integrated with AI-enabled analytics to increase throughput, reduce variability, and shorten DMTA cycle times. Ensures Data Quality & Scientific Rigor: Applies statistical methodologies to evaluate assay performance (e.g., Z’, variability metrics, curve-fit confidence) and ensures high-integrity data that directly informs compound progression and portfolio decisions.

Rahway, NJ26 days ago

Temporary
Contractor
Full-time

D. degree in chemistry, biochemistry or related scientific discipline with 5 years of industrial experience, OR Master of Science degree in chemistry, biochemistry or related scientific discipline with at least 10 years of industrial experience, preferably in a bioanalytical laboratory. Develop, validate and implement LC-MS/MS assays for the analysis of tissue, plasma and other biological samples to support pharmacokinetic, toxicokinetic, clinical efficacy and/or human food safety studies in a GLP environment.

New!

South Plainfield, NJToday

$70,000–$80,000 Per Year

Founded over 20 years ago and based in South Plainfield, NJ, we are an FDA-registered, cGMP-compliant analytical testing laboratory specializing in OTC drugs, pharmaceuticals, cosmetics, dietary supplements, and botanical products. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.

New!

Oakdale, MN4 days ago

$60,000–$70,000 Per Year

Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field with 3-5 years of relevant experience in a GxP regulated laboratory environment; or a Master's degree with 1-3 years of relevant experience. This role contributes to the development and validation of analytical methods, executes testing plans, and interprets data to support pharmaceutical and biopharmaceutical product development and quality control.

New!

Waltham, MA2 days ago

$90,000–$97,000 Per Year

See Pace Analytical Privacy Policy at https://www.pacelabs.com/privacy-policy/ and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions. A successful candidate will be able to quickly learn and independently operate instruments following training while contributing to efficient and reliable data acquisition.

New!

Indianapolis, IN6 days ago

$70,000–$100,000 Per Year

The QC Chemist will support all technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation and daily cleaning and maintenance activities, sample management and QC testing, and documentation completion and review in full compliance with GMP regulation, procedures, and product specifications. • Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow up and implementation, and Change Control management, including procedure and form revisions .

South San Francisco, CA30+ days ago

$98,000–$175,000

This model supports scientific entrepreneurs from the initial idea to clinical proof of concept (PoC) by combining a dedicated fund (TCG Labs) with our independent, evergreen R&D center led by a top-tier scientific team (Soleil). TCG Labs-Soleil does not accept unsolicited agency resumes and will not pay fees to any third-party agency or firm that doesn’t have a signed agreement with TCG Labs-Soleil.

Indianapolis, IN30+ days ago

Full-time

You will lead bioanalytical strategy, assay development, and execution for early research and development programs, providing critical data that advances Elanco’s innovation pipeline. Serve as the bioanalytical lead on cross-functional project teams, providing scientific and strategic guidance from early research through clinical development.

Waltham, MA29 days ago

Full-time

This LC–MS-focused role involves generating and interpreting data on oligonucleotide exposure, stability, metabolism, protein binding, and structural integrity to answer DMPK-relevant questions and link analytical findings with PK/PD and biological activity. Exposure & Disposition: Apply LC–MS and other methods to assess oligonucleotide–protein interactions, binding, and disposition, interpreting how stability, metabolism, and chemical modifications influence systemic and tissue exposure.

Cambridge, MA30+ days ago

Develop and oversee ligand-binding immunoassays (ELISA, MSD, Luminex or similar platforms) for the detection of translated proteins and anti-drug or anti-protein antibodies, including screening, confirmatory, and neutralizing antibody assays in accordance with regulatory guidance. You will be a subject matter expert in nucleic acid and protein bioanalysis, working to generate critical data that informs decision-making across preclinical and clinical development.

Durham, NC30+ days ago

Full-time

Cooperation: Displays positive outlook and pleasant manner; Establishes and maintains effective relations; Exhibits tact and consideration; Offers assistance and support to co-workers; Works actively to resolve conflicts; Works cooperatively in groups. · To perform the job successfully, an individual should demonstrate the following: · Communication: Exhibits good listening and comprehension; Expresses ideas and thoughts in written form; Expresses ideas and thoughts verbally; Keeps others adequately informed; Selects and uses appropriate communication methods.

New!

New Haven, CT4 days ago

Contractor

D. in Life Sciences or related field with 8 years of relevant laboratory experience or Bachelors/Masters degree in relevant scientific discipline with 15+ years relevant laboratory experience Good understanding of bioanalytical assay development, validation, and associated data analysis Working knowledge of regulatory guidance documents that pertain to the bioanalytical discipline Experience with immunoanalytical methods, LCMS based methods and cell culture technique based assays for discovery support Experience performing method development using Design of Experiments (DOE) and lab automation Experience in organizing and managing multiple bioanalytical projects in the laboratory setting Scientifically independent - design, execute, analyze, interpret results, and reaches correct conclusions Well organized, motivated, team player, and works with a sense of urgency Experience in transferring assays to CROs, monitoring development/validation, and sample analysis Good writing and oral communication skills including good presentation skills Managing colleagues, working effectively in project teams and providing technical input to colleagues Can lead an inter-department project or initiative involving other contributors Some duties of this role are conducted in an lab environment. The primary responsibilities include: (1) Lead an inter-department project or initiative involving other contributors; (2) Design and execution of innovative scientific experiments for development, validation and implementation of robust bioanalytical methods on various technology platforms in clinical and nonclinical study samples; (3) Develop and implement new and Client protocols to address specific issues and/or troubleshoot and improve current existing assay platforms towards being more robust and transferable.

Cambridge, MA17 days ago

$270,000–$300,000

This highly visible role will be accountable for the preclinical bioanalytical strategy, biomarker strategy, data quality, and regulatory readiness, ensuring successful EDIT-401 IND submission and Clinical Trial execution. As the Senior Director, Bioanalytical and Biomarker Development, you will: Lead assay development, qualification, validation, and execution for measuring drug product components, immunogenicity, biomarkers, and other analytes in biological matrices.

New!

Durham, NC5 days ago

Full-time

The Lab Technician will support the bioanalytical laboratory by performing routine sample preparation, assisting with day-to-day laboratory operations, and helping maintain a safe, organized, and compliant lab environment. Computer Skills: Microsoft Office (Word, Excel, PowerPoint, Access, Publisher, Outlook, Internet Explorer) No additional computer skills required.

Redmond, WA30+ days ago

Full-time

SystImmune is seeking an experienced and visionary Associate Director/Director of Bioanalytical Laboratories to lead, expand, and inspire our bioanalytical capabilities supporting preclinical and clinical programs in biologics and ADC development. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs).

Los Alamos, NM20 days ago

Due to federal restrictions contained in the current National Defense Authorization Act, citizens of the People's Republic of China-including the special administrative regions of Hong Kong and Macau-as well as citizens of the Islamic Republic of Iran, the Democratic People's Republic of Korea (North Korea), and the Russian Federation, who are not Lawful Permanent Residents ("green card" holders) are prohibited from accessing facilities that support the mission, functions, and operations of national security laboratories and nuclear weapons production facilities, which includes Los Alamos National Laboratory. The successful candidate will work with a team of scientists, technicians, and students on multiple projects ranging from characterizing chemical exposure, understanding biological effects of chemical/non-chemical stressors, and developing bio-sample analysis including method development, data acquisition, and data processing.

Los Alamos, NM20 days ago

Due to federal restrictions contained in the current National Defense Authorization Act, citizens of the People's Republic of China-including the special administrative regions of Hong Kong and Macau-as well as citizens of the Islamic Republic of Iran, the Democratic People's Republic of Korea (North Korea), and the Russian Federation, who are not Lawful Permanent Residents ("green card" holders) are prohibited from accessing facilities that support the mission, functions, and operations of national security laboratories and nuclear weapons production facilities, which includes Los Alamos National Laboratory. The successful candidate will work with a team of scientists, technicians, and students on multiple projects ranging from characterizing chemical exposure, understanding biological effects of chemical/non-chemical stressors, and developing biosample analysis including method development, data acquisition, and data processing.

Redwood City, CA30+ days ago

Full-time

This individual will play a key role in advancing preclinical oncology and immunology programs by designing, executing, and analyzing in vivo studies and mechanistic ex vivo assays to support target validation, candidate selection, and translational strategy.  . Perform and analyze multi-parameter flow cytometry experiments, including panel design, staining optimization, acquisition, and advanced data analysis to characterize immune and tumor cell populations  .

West Point, PA30+ days ago

D. in chemistry, biochemistry, or related scientific discipline with at least 3 years of industrial experience, or a Masters degree with a minimum of 7 years of relevant industry experience, preferably in a bioanalytical setting . Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies.

Rahway, NJ25 days ago

Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies. D. in chemistry, biochemistry, or related scientific discipline with at least 5 years of industry experience, or a Masters degree with 10+ years of relevant experience.

Waltham, MA30+ days ago

Full-time

You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. Collaborate: Work closely with internal/external partners on drug discovery projects to ensure studies are executed to meet scientific goals and timelines.

Natick, Massachusetts30+ days ago

$125,000–$155,000 Per Year

You will be responsible for: Analyzing scientific information to address microbiological, biological, and material science matters related to microbiological contamination root cause analysis, forensics, and product development, but also including a wide range of topics from medical devices and pharmaceuticals to consumer products and electronics. A strong theoretical and practical knowledge of various microbiological and biological assays (such as nucleic acid amplification tests, immunoassays, bacterial culture, protein quantification, and enzyme assays) and how material interactions can impact those techniques.

Cincinnati, Ohio24 days ago

Responsibilities : Develop and validate LC-MS/MS, GC-MS, ICP-MS, HPLC methods for small molecule drugs or drug metabolites and biomarkers; Draft study protocols/plans, acquisition methods, and study reports; Supervise all phases of bioassays to support pre-clinical and clinical pharmacokinetics, PD Biomarkers; Supervise technicians for performing method development, validation, and sample analysis; Communicate with internal and external resources for sample receiving, quality control, quality assurance, sponsor correspondence etc. Qualifications : PhD in Chemistry, Biochemistry, Pharmaceutical Sciences or related field; Previous experience with small molecule drug and drug metabolites analysis; Strong project management, compliance, communication, and people skills; Experience with various extraction procedures, such as LLE, SPE, SLE+, immune-capture hybrid extraction, etc.

Ridgefield, CT30+ days ago

$115,000–$181,000 Per Year

Experimental Medicine, BDS, CBOs, Clinical Operations, NCS Study Directors, and DMPK leads) for protocol development and review, sample handing, sample analysis plans, data transfers, milestones, report timelines, accurate budgeting, and other clinical/nonclinical requirements. Additionally, this role is responsible for the scientific monitoring and outsourcing of clinical and nonclinical bioanalytical studies, serving as the primary key contact and liason between DMPK, clinical trial teams, Nonclinical Safety, and bioanalytical CROs.

New Haven, CT30+ days ago

$90,900–$151,500 Per Year

Contribute to study design from the perspective of sample collection and processing through the following: Critical review and contribution to clinical protocols; Interaction with external study teams and/or the biomarker clinical assay lead (BCAL) to identify and resolve issues before study start; Management of resources to efficiently support studies and on the scheduled timelines. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.

Thousand Oaks, CA18 days ago

This group performs assays for small molecule and peptide analysis using LC-MS/MS, ELISA assays using MSD and Spectrmax readers and Immunogenicity assays that are Anti-drug antibody and Neutralizing Antibody assays using MSD, Spectramax, Envision and Vicell type readers. You will work closely with the global Pharmacokinetics and Drug Metabolism Bioanalytical Sciences (PKDM BA) team, collaborating with colleagues across sites in California and Germany, as well as with software vendors and internal subject matter experts.

Kansas City, KS25 days ago

Full-time

Our Mass Spec Bioanalysis Development team uses LCMS (Liquid Chromatography Mass Spectrometry) techniques to conduct sophisticated sample preparation to meet bioanalytical needs for drug discovery, preclinical, and clinical studies, including bioanalysis of drugs and metabolites, biomarkers, and active endogenous compounds in biological fluids and tissues. When you work as a Scientist II in the Mass Spec Bioanalysis Development group at KCAS, you get to further our mission by leveraging your knowledge in bioanalytical and scientific principles to independently execute defined aspects of studies, from study setup through data generation, as well as support development activities.

Kansas City, KS25 days ago

Full-time

Our Mass Spec Bioanalysis Development team uses LCMS (Liquid Chromatography Mass Spectrometry) techniques to conduct sophisticated sample preparation to meet bioanalytical needs for drug discovery, preclinical, and clinical studies, including bioanalysis of drugs and metabolites, biomarkers, and active endogenous compounds in biological fluids and tissues. When you work as a Sr Scientist in the Mass Spec Bioanalysis Development group at KCAS, you get to further our mission by leveraging your knowledge in bioanalytical and scientific principles to be responsible carrying out all aspects of a study, from study setup through reporting, as well as development.

Devens, MA30+ days ago

$124,590–$151,000 Per Year

Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Build effective relationships/partnerships and work cross-functionally with internal and external stakeholders to implement novel integrated automated systems to streamline execution and analysis of cell therapy assays.

Pearl River, NY30+ days ago

$90,900–$151,500 Per Year

Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Key responsibilities include designing and executing experiments in membrane filtration and column chromatography to purify diverse proteins, testing scale-up, ensuring the manufacturability of the process, and technology transfer.

Madison, NJ30+ days ago

$125,000–$153,000 Per Year

Full time Regular Colleague Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. The successful candidate will be primarily responsible for designing, conducting, analyzing, and interpreting in vivo PK/PD studies in multiple species in support of biotherapeutics (protein therapeutics) projects from early research through late-stage development.

Cambridge, MA30+ days ago

$152,730–$185,100 Per Year

In this role, you will represent the Dev DMPK function on cross-functional development project teams; oversee developmental drug metabolism and disposition, and non-clinical pharmacokinetics activities of multiple projects; be responsible for preparation of regulatory dossier / submissions; and assist in developing strategy for the group. Within the Pharmaceutical Candidate Optimization (PCO) organization at BMS, the Development DMPK Team provides ADME (absorption, distribution, metabolism, and excretion), DDI (drug-drug interactions) and PK (pharmacokinetics) support for all pipeline assets throughout clinical development, from candidate nomination through registration and lifecycle management.

Malvern, PA30 days ago

Full-time

The candidate's primary responsibilities will include but are not limited to the production, testing, inventory, and supply of Master, Working, and development Cell Banks for clinical, and commercial production as well as analytical testing for J&J biopharmaceutical and cell therapy products. Position Summary: The role of an Associate Scientist, BioTD-API Cell Banking will be to perform Cell Banking for the Cell Culture processes and/or bio-analytical testing within the API Large Molecule Process Development group in Malvern PA.

New!

Michigan5 days ago

Zoetis, a global leader in animal health, seeks an enthusiastic colleague to join our Veterinary Medicine Research and Development (VMRD) PK/PD Scientist Team to discover and develop novel therapeutics for veterinary medicine. The successful candidate will be primarily responsible for designing, conducting, analyzing, and interpreting in vivo PK/PD studies in multiple species in support of projects from early research through late-stage development.

Burlington, Massachusetts30+ days ago

$80,000–$95,000

Why This Role Matters:This position plays a critical role in advancing technologies that recover and reuse critical materials (e.g., lithium, rare earths), helping reduce reliance on traditional mining and enabling a more sustainable future. We are the heart of metals processing; we are the crucial step that profitably separates critical minerals from other elements, transforming them into production-grade feedstocks for the energy transition.

Kansas City, KS25 days ago

Full-time

nOur Mass Spec Bioanalysis Development team uses LCMS (Liquid Chromatography Mass Spectrometry) techniques to conduct sophisticated sample preparation to meet bioanalytical needs for drug discovery, preclinical, and clinical studies, including bioanalysis of drugs and metabolites, biomarkers, and active endogenous compounds in biological fluids and tissues. When you work as an Associate Scientist in the Mass Spec Bioanalysis Development group at KCAS, you get to further our mission by applying your knowledge in bioanalytical and scientific principles to support study execution and development activities with increasing independence.

Kansas City, KS30+ days ago

Full-time

As a Senior Scientist at KCAS Bio, you will serve as a lead technical contributor on complex bioanalytical studies, with the ability to independently execute and/or oversee all phases from study setup through final reporting, including method development and validation. In this role, you will act as a trusted internal expert, contributing to the advancement of scientific quality and operational efficiency while mentoring and developing less experienced scientific staff.

Kansas City, KS30+ days ago

Full-time

In this role, you will act as a recognized subject matter expert, shaping scientific strategy, establishing best practices, advancing innovation, and mentoring the next generation of scientific leaders, while representing KCAS Bio as a trusted scientific partner to clients, sponsors, and the broader scientific community. As a Principal Scientist at KCAS Bio, you will serve as the senior scientific authority within the assigned business unit, providing strategic leadership and ultimate accountability for the scientific quality and integrity of all assigned studies.

New!

San Diego, California5 days ago

$69,036–$89,570 Per Year

Responsibilities: Perform and be in charge of complex in vivo pharmacology experiments utilizing tumor models (syngeneic, xenograft tumor models and humanized mouse models) in both immunocompetent and immunocompromised mice; responsible for project execution, data update/presentation, and study report preparation. sterile cell culture techniques, and rodent handling experience (animal dosing (IV, PO, IP, SC), tumor implantation, blood/tissue collection, etc.) in academic or industry laboratory environment .

Seattle, WA30+ days ago

The successful candidate must have extensive hands-on experience in assay development and possess excellent communication skills in order to work on projects requiring close collaboration with other groups, such as discovery research, product sciences, process development, and QC. The Scientist will be responsible for developing impactful methods, including QC methods for lot release testing as well as characterization methods that support process development and comparability assessments.

New!

South San Francisco, CA2 days ago

Full-time

Lead context-of-use validation (in-house or through CLIA-certified laboratories or clinical CROs) of clinical biomarker assays suitable for use in recommended phase 2 dosing selection and/or regulatory submission. Liaise with nonclinical pharmacology and discovery immunology teams to establish proof-of-concept/proof-of-mechanism biomarker strategies suitable for use in NHPs and FIH studies.

New!

South San Francisco, CA2 days ago

Full-time

Familiarity with animal handling, survival blood draws (lateral tail vein, facial/maxilliary/submandibular), terminal blood draws (cardiac puncture), and dosing methods including i.v., s.c., i.p., and p.o. a must. Requirements: Bachelors degree with a minimum of 8 years of experience or Masters degree with a minimum of 6 years of experience in Immunology or other relevant life sciences (2 years must be in biotech or industry setting).

Oklahoma City, OK30+ days ago

PhD degree with no prior experience or Master’s Degree (in biochemistry, chemistry, microbiology, or other life-science discipline) with at least 2 years of relevant experience will be given consideration. Position Overview: Wheeler Bio is seeking a motivated analytical mind with a passion for problem solving, fast-paced environments, and expertise in protein mass spectrometry to join the analytical team.

Seattle, WA30+ days ago

The successful candidate must have hands on experience with various bioanalytical techniques including ELISA, qPCR, ddPCR and flow cytometry and the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Cell Therapy Product and Analytical Development (P&AD) is seeking an enthusiastic, self-driven (Senior) Associate Scientist to join its Critical Reagent Management team that values data quality, high productivity, and teamwork.

Milford, Massachusetts27 days ago

New!

Sterling, VA5 days ago

BluePath Labs is a fast-growing research and consulting company committed to solving complex problems for federal, state, and local government clients. BluePath's extensive experience in Government, Military, Commercial, and Academic environments is unique among small businesses and a core differentiator of our solutions.

Michigan23 days ago

The successful candidate will be primarily responsible for designing, conducting, analyzing, and interpreting in vivo PK/PD studies in multiple species in support of projects from early research through late-stage development. Zoetis, a global leader in animal health, seeks an enthusiastic colleague to join our Veterinary Medicine Research and Development (VMRD) PK/PD Team to discover and develop novel therapeutics for veterinary medicine.

Lawrence, KS30+ days ago

This position is responsible for support of CMC activities as well as working with Scientists and management for specific compound development at CritiTech in support of CritiTech product development and associated affiliates/partners for the global development and regulatory approval of New Chemical Entities (NCE’s), Active Pharmaceutical Ingredients (APIs) and support of research and development of any/all product activities. Communication Skills – ability to express one’s self clearly and concisely to CritiTech personnel over the phone or with others within the team; documents issues and/or concerns concisely and comprehensively; adjusts language and/or terminology appropriate for the audience.

Ayer, MA30+ days ago

100% Onsite! o Support in-process analytical testing for monoclonal antibodies, fusion proteins and AAVs, including HPLC/UPLC, isoelectric focusing, capillary electrophoresis, ELISA, qPCR, etc. o Authors and reviews technical documents and protocols; follows written scientific methods and experimental protocols, documents results, authors, and reviews summary reports.

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Bioanalytical Scientist Jobs in the United States

Jobs

Senior Scientist, High-Throughput Mass Spectrometry (Automation)Takeda Pharmaceutical

Associate Scientist, High-Throughput Mass Spectrometry (Automation)Takeda Pharmaceutical

Scientist - II (Associate)Genesis10

Chemist II – Analytical Chemistry (HPLC/GC, cGMP)Jobot

Experienced Analytical Chemist (Pharma)Pace Analytical Life Sciences

LC and LC/MS Analytical Chemist (Pharma)Pace Analytical Life Sciences

Lab Technician/ QC chemist/ Downstream Purification Technician/ Analytical ChemistSpectraforce Technologies Inc

Scientist, Bioanalytical and Translational Sciences (PK, ADA, Biomarkers)Soleil Labs, LLC

Principal Research Scientist, Bioanalytical (Large Molecule)Elanco

Scientist / Senior Scientist, Bioanalytical LC–MS – OligonucleotideAlloy Therapeutics

Senior Scientist, Bioanalytical SciencesCEDENT

Scientist/Senior Scientist- BioanalyticalMedPharm

Scientist II Bioanalytical DevelopmentIntegrated Resources, Inc

Senior Director, Bioanalytical and Biomarker DevelopmentEditas Medicine

Lab Technician I, BioanalyticalMedPharm

Associate Director/Director, Bioanalytical LaboratorySystimmune

Bioanalytical Chemistry and Mass Spectrometry Post-Bachelor StudentLos Alamos National Laboratory

Bioanalytical Chemistry and Mass Spectrometry Post-Master's StudentLos Alamos National Laboratory

Senior ScientistImmunEdge, Inc

Scientist IIJohnson Service Group

Scientist - II (Associate)Johnson Service Group

Research Associate / Associate Scientist – Oligonucleotide DiscoveryAlloy Therapeutics

Scientist (Ph. D.)Exponent Inc.

Small Molecule Bioanalysis ScientistMedpace, Inc.

Scientist IV, Drug Metabolism and PharmacokineticsBoehringer Ingelheim

Senior Scientist, Biomarker AssayPfizer

Associate ScientistThe Steely Group

Scientist II - Mass Spec DevelopmentIntegris BioServices, LLC dba KCAS Bioanalytical and Biomarker Services

Sr. Scientist - Mass Spec DevelopmentIntegris BioServices, LLC dba KCAS Bioanalytical and Biomarker Services

Principal Scientist, QC Assay Automation, Cell Therapy in Devens, MABristol Myers Squibb

Senior Scientist, Protein PurificationPfizer

PK/PD Principal ScientistZoetis

Senior Principal Scientist, Development DMPKBristol Myers Squibb

Associate Scientist, BioTD-API Cell BankingJohnson and Johnson

PK/PD Principal ScientistZoetis US

Analytical Chemist Materials ScientistNth Cycle

Associate Scientist - Mass Spec DevelopmentIntegris BioServices, LLC dba KCAS Bioanalytical and Biomarker Services

Sr Scientist - Mass Spec Bioanalysis Production (LC-MS/MS)Integris BioServices, LLC dba KCAS Bioanalytical and Biomarker Services

Principal Scientist - Mass Spec Bioanalysis Production (LC-MS/MS)Integris BioServices, LLC dba KCAS Bioanalytical and Biomarker Services

Scientist IWuXi AppTec

Scientific - Bio Analytical ScientistTechDigital Corporation

Senior Scientist, Translational ImmunologyParvus Therapeutics

Associate Scientist, In Vivo PharmacologyParvus Therapeutics

Analytical Development ScientistWheeler Bio, Inc.

Engineering - Assistant/Associate ScientistTechDigital Corporation

Senior Scientist PharmaWaters Corporation

Senior Scientist (Forensic/Analytical Chemist) - CBP (Onsite)BluePath Labs

PK/PD Senior ScientistZoetis US

Scientist I/Analytical ChemistCRITITECH PARTICLE ENGINEERING SOLUTIONS

Assistant/Associate ScientistTechDigital Corporation

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