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  • Senior Principal Applied Scientist - Telecommute

    UnitedHealth Group is a company that's on the rise. Optum Labs is looking for a Senior Principal Machine Learning Scientist with deep subject matter expertise in the area of image processing, NLU and SLU (Natural language understanding and Spoken Language Understanding) who will lead the technical development and inventions that allow Optum machine learning products drive positive impact in the healthcare business. (sm) Optum Labs is the research and development arm of UnitedHealth Group.
    $113.5k-218.1k yearly60d+ ago
  • Scientist I, Biomarker Assay Development, Translational Science

    At Horizon Therapeutics, we define success by the number of lives touched, lives changed, and lives saved.
    $58k-88k yearly est.5d ago
  • Vulnerability Research and Development - US Citizens

    Zetier hires skilled engineers and non-technical experts that are driven by mission success. To prevent limiting world-class talent to a single project, technical domain, or target space at Zetier we consider your full potential, background, and interests and align that to an engineering grade of Junior, Journeyman, Senior, xor Principal. Desired Technical Domains at Zetier:
    $74k-105k yearly est.23d ago
  • Principal, Research - Remote

    * Learn and execute Gartner's proven methodology for conducting world-class research that helps identify best practice solutions to many of today's biggest customer service challenges, including cross topics such as service and support strategy, talent, customer experience (CX), and digital channels Gartner Researchers support the discovery of actionable business ideas while bringing best practices, and research models to life across a broad range of world-leading clients.
    $103k-128k yearly est.38d ago
  • Principal Research Scientist - Health Care Policy Research - Remote or Hybrid

    NORC at the University of Chicago seeks a qualified Principal Research Scientist to direct program and policy projects related to Medicare and/or Medicaid, including projects involving policy analysis, focus groups, literature reviews, structured interviews with stakeholders including health care providers, insurers, policymakers, and patients, and quantitative analysis.
    $72k-102k yearly est.60d+ ago
  • URGENT Formulation Scientist

    Job DescriptionDescription: JOB SUMMARY Under general supervision, performs formulation activities as required for, but not limited to, oral, transdermal, topical, oral, nasal, and ophthalmic route projects. Carries out laboratory work to support product formulation and development, stability work, excipient, and packaging sourcing. Job Responsibilities: * Developing complex pharmaceutical products, leading to successful ANDA filings and approval in a timely manner. * Managing and scheduling multiple projects, setting objectives, prioritizing activities to meet the milestones in a fast pace environment. * Designing, formulation and process development for various drug from project initiation to commercialization by following appropriate GMP regulations and safety requirements. * Participate in the set-up and operation of pilot scale equipment and instrumentation for the completion of small production runs in collaboration with the R&D technician. * Design and conduct pre-formulation and formulation studies, process development and optimization of prescription dosage form designs and ANDA oral Dosage forms using DOE * Perform Literature search and Evaluate patents to develop non-infringing strategies * Preparation of product manufacturing, batch records and protocols for different product development stages, including from R&D prototype formulations to process validations following SOPs and procedures, ensuring the detailed record and data keeping. * Utilize formulation techniques, processing equipment and unit operations including Wurster Coating, Tablet Coating, Compression, Blending, Encapsulation, HPLC, Spectrophotometry, Dissolution, Viscometer to develop Bio-Equivalent products * Review Analytical Data, draft SOP's, Process Evaluation protocols, IQ, OQ, PQ protocols and GMP Manufacturing Batch records, Packaging Batch Records. * Characterization of APIs, excipients and in process products; analysis of in-process samples or in-process products based on protocols and QbD concept, preparing various formulation samples to support cross-functional programs as needs. * Setting-up and cleaning equipment for experiments by following the SOPs, maintaining formulation Lab in a clean and safe working environment. * Establishing documentation management systems for CMC development and meeting FDA GMP, regulatory requirement, and FDA onsite inspections. * Comprehensive knowledge of Quality by Design (QbD) and Design of Experiments (DOE). * Professional knowledge of manufacturing principles, theories, and techniques. * Ensuring all regulatory documents in compliance with SOPs, FDA Regulations, and cGMP policy where applicable. OTHER or ADDITIONAL RESPONSIBILITIES Documentation * Completes documentation associated with manufacturing processes (e.g. batch record, protocols, and logbooks) with detail and accuracy. * Meets requirements for entries on all applicable Batch Production pages, completion and attachment of all dispensary and weight verification tickets. * Verifies the manufacturing process on BPR in an accurate and timely manner. * Provides status updates and operational challenges on status boards. Continuous Improvement * Assists in troubleshooting process issues; refers deviations from standard procedure to the supervisor. * Typically participates in at least one continuous improvement project of a moderate scope and complexity. Safety & Compliance * Adheres to all cGMP compliance/regulatory mandates and quality requirements. * Participates in safety teams, start-up discussions, incident debriefing sessions, etc. * Ensures compliance with SOPs, policies and procedures as required by the Company and regulatory agencies. * Maintain a clean, organized, work area. Training * Conforms to all training requirements, including company required and machine-specific training. Teamwork & Collaboration * Contributes to team and project success by sharing previously acquired knowledge. * Collaborates typically within own cross-functional work unit and occasionally with contacts outside own unit or department. Preferred Knowledge & Skills: * Knowledge of manufacturing regulatory programs and objectives (cGMP, CFR 210 and 211). * Maintaining formulation development notebook document work. * Maintaining compliance with GMP, SOPs and DEA regulations. * Coordinate with Regulatory Affairs, Operations, QC/QA, and Supply Departments to ensure that projects are planned and executed in a timely manner. Education & Experience: * BS or MS in Chemistry, Pharmacy, Biochemistry, Biology or Bio-technology or related field. * 2-3 years of experience in core formulation development and analytical instrument techniques. Physical Requirements/Working Environment: * Must be able to stand for long periods of time (up to 12 hour shifts), maneuver at least 50 pounds, climb ladders, wear a respirator and pass associated respirator tests and/or requirements, and be able to wear all required PPE, including safety glasses, ear plugs, and safety shoes * Stand, W
    $69k-103k yearly est.29d ago
  • Sr Principal, Semiconductor Packaging

    MITRE Engenuity is a non-for-profit tech foundation created by the MITRE Corporation to undertake complex challenges that neither government nor industry can solve on their own. If this sounds like the choice you want to make, then choose MITRE-and make a difference with us. At MITRE, you can have both. MITRE is different from most technology companies. That's because MITRE people are committed to tackling our nation's toughest challenges-and we're committed to the long-term well-being of our employees. * Analyzing and developing strategic proposals in support of MITRE Engenuity initiatives in semiconductors, spanning business models, technology, investments, and innovation.
    $166k-207.5k yearly17d ago
  • Force Development Scientist & Engineer (S&E) Manager

    Job DescriptionQED Enterprises (QED) was founded on the principles that we provide Quality services to our clients; we strive for Excellence in all that we do; and we are Driven to meet our customers' missions on time, within budget, and with the exceptional attention to detail our customers have come to expect of QED. QED Enterprises, Inc. (QED) is an SBA certified 8(a) small business and a Department of Veterans Affairs Center for Verification and Evaluation (CVE) certified service-disabled veteran-owned small-business (SDVOSB). Title: Force Development Scientist & Engineer (S&E) Manager - Subject Matter Expert Location: Arlington, VA *** MUST BE WILLING TO WORK ON SITE EVERY DAY *** Clearance Level: Secret Summary/Description: This position supports overarching acquisition workforce management as well as career field management for scientists, development engineers and program managers.
    $73k-106k yearly est.33d ago
  • Downstream Scientist - mRNA purification

    Site Name: USA - Maryland - Rockville, USA - Delaware - Dover , USA - Delaware - Wilmington, USA - Virginia - Arlington, Washington DC
    $55k-82k yearly est.40d ago
  • Lead Scientist I - Immunochemistry (Hybrid Work Model)

    **Schedule:** This position will allow for the majority of the work week to be remote based with an on site presence in Chantilly 1 day out of the week following initial training/onboarding. The **Lead Scientist** supports the Immunochemistry team within the Bioanalysis division in Chantilly, VA. This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner, as Labcorp Drug Development has helped pharmaceutical and biotech companies develop one-third of all prescriptions medicines in the market today. At Labcorp, we offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. **What Labcorp Drug Development can offer you:** As the Lead Scientist, you will act as the Study Director, Responsible Scientist, or Principle Investigator for non-regulated, GLP-regulated, and GCP-regulated bioanalysis studies.
    $93k-118k yearly est.60d+ ago
  • Principal Research Scientist (Systems Tactics and Forces Development)

    2. Operate as a recognized expert in a specific field/research area within CNA; leverage that expertise to enhance CNA's reputation with existing clients/sponsors. Operate as a senior researcher at CNA HQ or in the field. Play a lead role in enhancing CNA's reputation as an organization. Play a lead role in efforts to enhance CNA's reputation via publishing and outreach activities.
    $114k-147k yearly est.40d ago
  • Chief Scientist, Artificial Intelligence and Machine Learning

    The Chief Scientist will engage with universities to identify relevant emerging new technologies, promote research directions aligned with LM strategic roadmaps, create new partnerships with faculty for joint research projects, and strengthen future talent pipeline for ATL. The Chief Scientist will also engage with US Gov. The Chief Scientist for Artificial Intelligence and Machine Learning .AI/ML. will drive creation of relevant long.term technology roadmaps for ATL, propose internal investments to build new capabilities, create new strategic partnerships with universities, commercial companies, and US government R&D organizations, and support acquisition of new business. It is expected that initial focus of the Chief Scientist will be on Neuro.Symbolic Reasoning applied to sense making in autonomy and battle management. To ensure alignment with LM Business Area .BA. strategies, the Chief Scientist will work closely with senior technical staff .including LM Fellows. from ATL, LM Artificial Intelligence Center .LAIC., and LM BA R&D organizations to create long.term AI/ML roadmaps. **Description:** The Advanced Technology Laboratories .ATL. is a Lockheed Martin applied research and development center. To help build new AI/ML capabilities within ATL, the Chief Scientist will lead definition of the technical content for strategic AI/ML internal R&D projects and be responsible for the quality of their execution.
    $74k-113k yearly est.60d ago
  • Clinical Application Scientist

    CooperSurgical is a leader in manufacturing and marketing multiple trusted and innovative brands that assist clinicians in improving the health of women, babies and families worldwide. * Support the Global scientific communication profile with inputs to White papers and ART Scientific * Work closely as part of the global Medical Affairs team, to ensure alignment of activities and sharing of global best practices. For U.S. locations that require disclosure of compensation, the starting base pay for this role is between $$110,000 and $180,000. * Participate in the global online training program offering by Medical Affairs * Run local workshops and training in collaboration with the Account Managers, senior CAS, Marketing and Medical Affairs * Bring back insights from clinic visits to Marketing to help the Commercial team identify opportunities for improved partnership with clinics All resumes submitted by search firms/employment agencies to any employee at CooperSurgical via-email, the internet or in any form and/or method will be deemed the sole property of CooperSurgical, unless such search firms/employment agencies were engaged by CooperSurgical for this position and a valid agreement with CooperSurgical is in place. The actual base pay includes many factors, and is subject to change and modification in the future. * Work closely with the Americas Marketing team to ensure alignment of activities and time allocation/prioritization with broader business priorities.
    $110k-180k yearly7d ago
  • Scientist I, Biomarker Assay Development, Translational Science

    At Horizon Therapeutics, we define success by the number of lives touched, lives changed, and lives saved.
    $58k-88k yearly est.1d ago
  • Staff Applications Scientist

    This role is based in Guardant Health's San Diego office. The Guardant Health oncology platform leverages capabilities to drive commercial adoption, improve patient clinical outcomes and lower healthcare costs across all stages of the cancer care continuum. Additional Information Hybrid Work Model : At Guardant Health, we have defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. Guardant Health is a leading precision oncology company focused on helping conquer cancer globally through use of its proprietary tests, vast data sets and advanced analytics. The Guardant Health screening portfolio, including the Shield test, aims to address the needs of individuals eligible for cancer screening. Guardant Health has commercially launched Guardant360 , Guardant360 CDx, Guardant360 TissueNext , Guardant360 Response , and GuardantOMNI tests for advanced stage cancer patients, and Guardant Reveal for early-stage cancer patients. About the Role: As a Staff Application Scientist, you will be responsible for validating and improving the 'sample to reporting' workflow on the newly launched Guardant Infinity platform to serve the needs of GH lab customers. Job Description Department Summary- The Global Technology transfer team is focused on implementing Guardant Health workflows at leading cancer centers in the EU and AMEA through licensing its technology and supporting patients/biopharma companies from that region.
    $139k-188k yearly1d ago
  • Senior Associate Data Scientist (US - Remote)

    The Biosimilars Business Unit Process Development (BBU-PD) is a dynamic group that works with a diverse range of cross-functional groups to develop Amgen biosimilar products by evaluating them for analytical similarity, a foundation of the biosimilar regulatory pathway. At Amgen, our shared mission-to serve patients-drives all that we do.
    $97.7k-125.4k yearly49m ago
  • Head of Product Growth (Mobile Games Live Ops) (f/m/d)

    We receive immense support to achieve this goal through the AppLike Group.
    $72k-99k yearly est.19d ago
  • Scientist 3 - Protein Biochemistry

    Genentech requires all new hires to be fully vaccinated against COVID-19 as of their start date. The expected salary range for this position based on the primary location of South San Francisco, CA is $98,200 and max of $182,400. The Department of Physiological Chemistry at Genentech is seeking a talented and motivated protein biochemist to drive structure-function studies of challenging membrane proteins involved in cell death and inflammation.
    $98.2k-182.4k yearly19m ago
  • Force Development Scientist & Engineer (S&E) Manager

    * Supporting the Air Force career field management and force development processes for the civilian and officer program management, scientist, and engineer career fields.
    $67k-93k yearly est.39d ago
  • Scientist 2, Enterprise Data Analytics & Data Intelligence

    Comcast Technology Solutions is a fantastic place for bright minds and forward-thinkers looking to innovate and evolve with a company they can be proud of. (In most cases, Comcast prefers to have employees on-site collaborating unless the team has been designated as virtual due to the nature of their work. Make your mark at Comcast -- a Fortune 30 global media and technology company. Comcast Technology Solutions, a division of one of the world's leading media and technology companies, brings Comcast Corporation's proven technologies to an evolving list of industries worldwide. You'll do the best work of your career right here at Comcast. Our roots - and our hearts - are in broadcast and digital video, but as part of Comcast NBCUniversal, we are so much more.
    $87.9k-131.8k yearly16d ago

Average Salary For a Senior Food Scientist

Based on recent jobs postings on Zippia, the average salary in the U.S. for a Senior Food Scientist is $72,882 per year or $35 per hour. The highest paying Senior Food Scientist jobs have a salary over $120,000 per year while the lowest paying Senior Food Scientist jobs pay $43,000 per year

Updated June 6, 2023
Average Senior Food Scientist Salary
$56,188 yearly
$35 hourly

1 Common Career Paths For a Senior Food Scientist

Product Development Manager

A product development manager spearheads the development of new products within a company. Most of the time, their responsibilities revolve around conducting marketing research and analysis to determine consumers' needs, coordinating with the product development team to come up with new ideas, proposing business plans to the executives, and creating prototypes. A product development manager must also present a cost analysis, produce progress reports, and address inquiries and concerns. Furthermore, as a manager, it is essential to lead and encourage the staff, all while adhering to the company's policies and regulations.

Illustrated Career Paths For a Senior Food Scientist