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Job Description Contract: 2 Years (Renewable) Compensation: Location: Summit, NJ – Hybrid – Onsite 2-3 days a week. Job ID: 749 Pay Rate: $35/hr. W2 Team: Product Development Team Office based role This role will require knowledge of product development from a regulatory perspective. The role will be shortlisted on Monday. Top Skills: 1. Collaborate with cross functional teams and pull data, 2. Organize and follow up Interview Process: 1. First round will be virtual, 2. Second round will be a panel. This worker will report to a Scientist on a team so the 2nd round will include the report-to manager and 3 other team members We are seeking an independent and motivated Scientist to join the Product Development R&D team. This role will report into Product Development in the US and will be responsible for launches in Canada. This role focuses on the technical evaluation and execution of products in the Canadian market. The Senior Scientist will have full responsibility for documentation and product development activities of mid-to-low complexity projects. The ideal candidate will have a background in formulation science, process development, and experience in GxP (e.g. GDP, GMP, GCP) compliance. Key Responsibilities: · Act as the Product Development representative for regional projects, attend meetings and answer questions as the technical point of contact for PD Canada. · Contribute to project planning, timeline management, and project milestone deliverables to ensure successful project. · Work closely with cross-functional teams, including other R&D functions, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals. · Conduct product feasibility for Canada, review existing data and determine if any gaps, connect with EM sites or US teams on formulation options · Generate documentation and specifications needed for regulatory clearance and product launch. · Prepare and maintain detailed documentation for product development processes, including experimental protocols, and technical reports in compliance with Good Documentation Practices (GDP) Degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related field. · trong knowledge of formulation science, ingredients functionality and compliance, and consumer product market. . Understanding of regulatory landscape and requirements for personal care products. · Excellent written and verbal communication skills, with the ability to present complex information clearly and concisely. · Ability to work collaboratively within multidisciplinary teams and matrixed organization. · Strong analytical and problem-solving skills, with high attention to detail . Education/Experience: Ph.D. in Pharmaceutical Sciences +0-2yr, M.S. with 3+ years of relevant experience, or Bachelor’s Degree Experience in product and process development within the consumer health industry. Demonstrated ability to manage multiple projects and work effectively in a fast-paced environment. · Proficient Excel skills Company Descriptionwww.techdataservice.comwww.techdataservice.com

Job DescriptionAbout Dyania Health Dyania Health is a venture-backed company founded in 2019 which has developed Synapsis AI, an end-to-end system that combines a medically post-trained LLM with a physician-driven algorithmic reasoning engine to understand and assess clinical characteristics in electronic medical records. Synapsis AI is designed for installation within the healthcare system's computing environment or on healthcare system private clouds to automate manual chart review of EMRs without removing any data from the healthcare system. Synapsis AI completes pre-screening on both unstructured and structured patient data, deploying medical logic with temporal sensitivity to dynamically match changing patient characteristics to complex clinical trial criteria within the exact window when a given EMR may qualify for study protocol criteria. The Role We are seeking a Staff or Senior Staff Research Scientist to lead the design, development, and implementation of advanced AI/ML and LLM-based models for clinical data understanding. This is a senior, hands-on research role. You will build and customize models, design architectures, and drive ML innovation from concept through production. This is not a data science or analytics role—we are looking for someone who deeply understands how models work internally and can independently solve complex, open-ended problems. Leveling is based on experience: • Staff Research Scientist: 7+ years of relevant experience, • Senior Staff Research Scientist: 10+ years, including technical leadership responsibilities What We’re Looking For • A senior researcher who builds models, not dashboards, • A hands-on technologist who understands model architecture, training, and optimization, • Someone who can define strategy, lead initiatives, and still write production-quality code, • A strong independent problem solver comfortable with ambiguity and research-driven development, • A technical leader who can mentor others while delivering individually Key ResponsibilitiesResearch, Development & Implementation • Design, build, train, and deploy AI/ML and LLM-based models, • Own the full model lifecycle: problem definition, research, prototyping, training, evaluation, and deployment, • Apply strong understanding of ML and AI fundamentals to real-world biomedical problems, • Develop and optimize models using Python and modern ML frameworks, • Research emerging techniques and propose innovative solutions aligned with product and business needs Problem Solving & Strategy, • Independently analyze complex, ambiguous problems and determine appropriate modeling approaches, • Evaluate and recommend technical solutions and system architectures, • Translate research concepts into scalable, production-ready systems, • Contribute to long-term ML and AI strategy and technical vision Leadership, • Lead cross-project research and development initiatives, • Provide technical mentorship and guidance to junior researchers and engineers, • Establish best practices for experimentation, model development, and deployment, • Influence technical roadmaps and architectural decisions Requirements Required Qualifications • 7+ years (Staff) or 10+ years (Senior Staff) of experience in AI/ML research or ML engineering, • Graduate degree in Computer Science, Engineering, or a related technical field, • Strong hands-on experience building, training, and deploying ML and AI models, including LLMs, • Deep understanding of model fundamentals and architecture design, • Proven ability to solve problems end-to-end, from research through implementation, • Advanced proficiency in Python for model development and training, • Experience customizing models rather than relying solely on pre-built solutions, • Ability to independently research, evaluate, and propose technical approaches Preferred Qualifications • Publication record in top-tier AI, NLP, or ML conferences, • Experience working with EMR or other complex clinical datasets, • Experience with multi-modal AI systems, • Prior senior or lead-level technical experience, • Familiarity with regulatory considerations for clinical AI systems, • Experience contributing to long-term technical strategy or system architecture, • PhD is welcome but not required Team Culture: • We lead with empathy for patients and our teammates, • We value small egos, self-awareness, and humility in our teammates, • We appreciate flexible and adaptive attitudes towards solving problems, as strategic priorities may shift, • We love diversity of thought, perspective, working style, skill set, knowledge, and interests amongst our team, • We value open dialogue and brainstorming across multidisciplinary teams Dyania Health is an equal opportunity employer that is committed to workplace diversity and inclusion. We do not discriminate on the basis of race, gender, gender identity, color, religion, national origin, sexual orientation, or any other legally protected characteristic as outlined by federal, state, or local laws. Benefits • Competitive Salary, • Health Care Plan (Medical, Dental & Vision), • Retirement Plan (401k, IRA), • Generous Paid Time Off (Vacation, Sick & Public Holidays), • Family Leave (Maternity, Paternity), • Training & Professional Development Support, • Remote work

Job Description Job Title: Sr Scientist Product Development R&D Location: Summit NJ 07901 Duration: 05/26/2026 to 05/24/2028 Role Overview: This is a technical role within the Product Development Formulation team, focused primarily on documentation and compliance support rather than laboratory or formulation work. Key Responsibilities: • Work closely with the Lab and Product Development teams, • Review, read, and understand product development documentation, • Handle extensive documentation and paperwork activities, • Prepare product development reports, • Update specifications, SKUs, and related product documentation, • Support documentation requirements for the Canadian market, • Ensure coordination with cross-functional teams, • Perform data analysis, identify data gaps, and ensure compliance with Canadian regulations, • Participate in project planning and team meetings, • Support multiple brands/segments Required Background: • Technical background preferred, • Experience with product launch documentation strongly preferred, • Strong understanding of product development documentation processes, • Knowledge of Canadian industry regulations and compliance requirements Important Notes: • This role is documentation focused and does not involve formulation or lab wor Description: • We are seeking an independent and motivated Scientist to join the Product Development R&D team., • This role will report into Product Development in the US and will be responsible for launches in Canada. This role focuses on the technical evaluation and execution of products in the Canadian market., • The Senior Scientist will have full responsibility for documentation and product development activities of mid-to-low complexity projects. The ideal candidate will have a background in formulation science, process development, and experience in GxP (e.g. GDP, GMP, GCP) compliance. Key Responsibilities: • Act as the Product Development representative for regional projects, attend meetings and answer questions as the technical point of contact for PD Canada., • Contribute to project planning, timeline management, and project milestone deliverables to ensure successful project., • Work closely with cross-functional teams, including other R&D functions, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals., • Conduct product feasibility for Canada, review existing data and determine if any gaps, connect with EM sites or US teams on formulation options, • Generate documentation and specifications needed for regulatory clearance and product launch., • Prepare and maintain detailed documentation for product development processes, including experimental protocols, and technical reports in compliance with Good Documentation Practices (GDP), • Degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related field. ·, • Strong knowledge of formulation science, ingredients functionality and compliance, and consumer product market., • Understanding of regulatory landscape and requirements for personal care products., • Excellent written and verbal communication skills, with the ability to present complex information clearly and concisely., • Ability to work collaboratively within multidisciplinary teams and matrixed organization., • Strong analytical and problem-solving skills, with high attention to detail . Education: • Ph.D. in Pharmaceutical Sciences +0-2yr, M.S. with 3+ years of relevant experience, or Bachelor’s Degree, • Experience in product and process development within the consumer health industry., • Demonstrated ability to manage multiple projects and work effectively in a fast-paced environment. ·, • Proficient Excel skills

Job Description Kenvue is currently recruiting for a: Senior Scientist Product Development What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role reports to: RESEARCH MANAGER Location: North America, United States, New Jersey, Summit Work Location: Hybrid What you will do We are seeking a motivated and experienced Senior Scientist to join Self-Care Product Development team. Reporting directly to a Manager in the Product Development team, this role focuses on supporting the development and optimization of consumer health products, with an emphasis on over-the-counter (OTC) medications and supplements. The Senior Scientist will play a critical role in ensuring product efficacy, safety, and compliance with regulatory standards. The ideal candidate will have a strong background in formulation science, process development, and experience in GxP (e.g. GDP, GMP, GCP) compliance. Key Responsibilities Lead consumer centric formulation and development of consumer health products, including OTC medications, dietary supplements, and personal care items, ensuring they meet quality and efficacy standards. Exercise considerable latitude in determining technical objectives and in selecting techniques and evaluation criteria for obtaining resolution to complex and dynamic problems in consultation with manager. Identify and resolve technical challenges in product and process development, utilizing sound scientific principles and experimental data under general guidance. Support the optimization of manufacturing processes to enhance efficiency, scalability, and robustness. Contribute to project planning, timeline management, and project milestone deliverables to ensure successful project. Work closely with cross-functional teams, including R&D, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals. Stay up-to-date with the latest scientific advancements and incorporate them into research projects Prepare and maintain detailed documentation for product development processes, including experimental protocols, batch records, and technical reports in compliance with Good Documentation Practices (GDP) What We Are Looking For Required Qualifications Degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Materials Engineering, Biomedical Engineering, Biophysics, or a related field. Ph.D. in Pharmaceutical Sciences +0-2yr, M.S. with 3+ years of relevant experience, or Bachelor’s Degree with 4+ years of relevant experience. Experience in solid dose formulation and manufacturing (tablets). Experience in formulation of liquid for ingestion. Strong knowledge of formulation science, process development, and foundational understanding of regulatory requirements for OTC medications and dietary supplements. Proficiency in analytical techniques and methods used in product development and quality control. Excellent written and verbal communication skills, with the ability to present complex information clearly and concisely. Ability to work collaboratively within a multidisciplinary team and across various functions. Strong analytical and problem-solving skills. Desired Qualifications Experience in product and process development within the consumer health industry. Experience in solid dose formulation and manufacturing (capsules, soft chews, gummies). Experience in formulation of semi-solids for ingestion, topical, and/or nasal application. Demonstrated ability to manage multiple projects and work effectively in a fast-paced environment. Proficiency in project management skills, including timeline management, budget oversight, and team coordination. What’s in it for you Annual base salary for new hires in this position ranges: $105,400.00 - $148,800.00 This takes into account a number of factors including work location, the candidate’s skills, experience, education level & other job-related factors. Competitive Benefit Package* Paid Company Holidays, Paid Vacation, Volunteer Time & More! Learning & Development Opportunities Kenvuer Impact Networks This list could vary based on location/region *Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on merit without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Job Description Summary: PLEASE NOTE - This is NOT a technical role for a Data Analyst, Data Scientist or someone with an IT background. Candidates MUST have experience in the Market Data realm and be able to administer Market Data contracts. Please read the description before you apply The Market Data Analyst at S4 Market Data will oversee client projects and be responsible for the overall service delivery of our managed services with respective clients. This position will manage market data service inquiries and projects from clients as well as manage a market data administrator within the projects to ensure administrative tasks are being completed in an accurate and timely manner. The ideal candidate will have market data vendor management and administrative experience; sourcing and negotiating contracts, managing procurement/sourcing requests throughout the spend life cycle, speaking with internal business units and stakeholders (legal, finance, IT, etc.) to procure goods/services for our clients. The candidate needs to be located in the US, this is a fully remote position. Responsibilities: • Handle day-to-day demand management or vendor management and administrative inquiries from internal business units, including but not limited to; data/sourcing requests, contract negotiation, entitlement administration, exchange reporting, moves/adds/changes requests, inventory management, procurement/legal approval, expense allocation, invoices reconciliation, and spend reporting., • Interact with the client’s various internal stakeholders and business units; technology, legal, accounting/finance, human resources, and investment managers., • Oversee the inventory management process of leavers/joiners, ensure current inventory is accurate and up-to-date. Oversee the reconciliation invoices and validation of monthly allocations/expenses., • Conduct monthly/quarterly exchange reporting and ensure exchange policies and data compliance across the client’s end-users and applications. Administer their datafeeds (EMRS, DACS, Etc.), • Review spend and enact cost savings and avoidance initiatives. Provide respective business units with an overview for their costs; understand their products/services and respond to any inquires as needed. Maintain reports on costs and identify ways to consolidate spend., • Conducts regular internal team meetings to report on client SLA’s and to ensure all client service deliverables are being met and completed. Qualifications: • Bachelor’s degree in MIS, Business, or related degree and 3-5 years of relevant experience in financial services or market data. Relevant work experience in consulting is preferred., • Experience working with Market Data vendors such as Bloomberg, FactSet, Exchanges (NYSE, ICE, etc.)., • Knowledge of FITS and MDSL inventory systems is preferred., • Excellent communication and project management skills and experience in working closely with internal client business units and senior stakeholders., • An entrepreneurial and self-regulating mind-set. Display a high level of time management skills to manage multiple and elaborate requests simultaneously., • Have high energy and be a self-starter with the ability to work independently and as part of a team. Powered by JazzHR CqzWdPMF1h

Amazon is hiring a Principal Applied Scientist in Newark, NJ, to design and deploy data-driven models for machine learning applications.

Job Overview Join the Device Development & Technology (DD&T) Team focused on the design, development, and commercialization of novel biologic/drug/vaccine-device combination products. The Associate Principal Scientist will provide end-to-end technical and project leadership for the definition, integration, and execution of comprehensive testing strategies. This role emphasizes design verification while covering test method development, analytical transfers, incoming testing, in-process, release testing, and readiness activities to support successful clinical introduction and commercialization. Principal Responsibilities • Lead, set direction, align with key stakeholders, and successfully execute design verification strategies for assigned drug-device combination product programs for clinical introduction and market approval., • Define design input(s)/output(s) and lead the associated design verification plan, protocols, and reports that demonstrate design output(s) meet design input(s)., • Lead establishment of test methodologies, including method development and validation, internally or externally, per the design verification strategy., • Lead strategy and execution of accelerated and real-time aging studies, including bridging studies at the device component, subassembly, in-process material, and combination product levels., • Lead testing readiness and execution for critical activities such as stability studies, drug product filling process validation, combination product final assembly process validation, and shipping studies., • Support establishment of incoming and release tests at the component and combination product levels with key functional areas., • Oversee design verification activities performed by external partners., • Proactively anticipate and resolve project obstacles; communicate complex technical challenges, timelines, milestones, and risks within the company and with external partners., • Author and review relevant portions of regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs under your leadership., • Lead or support clinical supplies production with respect to device component and combination product testing., • Maintain a high level of engagement with cross-functional team members to implement and execute design verification strategies., • Stay current with new device technologies, worldwide regulations, standards, and share this knowledge with others., • Enhance the Company's professional image and competitive advantage through publications, presentations, patents, and professional activities. Qualifications • B.S. in Mechanical Engineering (or equivalent) + 8 years of combination product development experience; M.S. + 5 years; or Ph.D. + 3 years., • Leadership experience of combination product design verification programs and leading cross-disciplinary project teams., • Comprehensive knowledge of device development aspects and their interdependencies with design verification, including design controls, risk management, materials & molding, process development and validation, secondary packaging, and design validation., • Comprehensive understanding of drug product development in addition to device development expertise., • Strong familiarity with regulatory landscape associated with drug-delivery combination products and design verification requirements., • Strong working knowledge of relevant standards (ISO 11608, ISO 11040, ISO 80369, etc.) and performance tests related to container closure integrity and dose accuracy., • Proven track record of applying analytical skills in product test method design, development, and validation., • Working knowledge of analytical test method technology transfer processes., • Skilled in laboratory good documentation practices and electronic documentation systems., • Self-motivated ability to work independently., • Proven ability to lead teams across multiple disciplines and backgrounds., • Strong interpersonal skills and strategic thinking; ability to influence without formal authority and present ideas to senior leadership., • Excellent communication, prioritization, presentation, negotiation, project management, and organizational skills. Preferred Experiences • Experience with combination product drug delivery device components (plastic, metal, glass, elastomeric) and characterization methods such as fracture, stress-strain response, friction, hardness, surface roughness, and surface energy., • Experience with sub-assemblies (including electro-mechanical) and system tear-down analysis, gear-ratio optimization, weakest-link component identification, and optimization., • Material characterization and failure mode analysis integrated with risk management., • Stress-strain testing of different materials under varied environmental conditions (temperature, humidity)., • Eagerness to identify laboratory capability gaps, drive procurement of new equipment, and train others., • Experience with analytical or numerical simulation., • Excellent collaboration and ideation skills, including facilitation of brainstorming, proof-of-concept development, and feasibility data generation., • Familiarity with compression/tensile testing instruments and metrology/non-destructive inspection techniques., • Experience in 3D CAD (SolidWorks) and rapid manufacturing techniques for fixture development and device redesign. Salary & Benefits The salary range for this role is $142,400.00 – $224,100.00. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. Benefits include medical, dental, vision, retirement (401(k)), paid holidays, vacation, and other standard insurance and wellness programs. Equal Employment Opportunity As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other protected characteristics. We are a federal contractor and comply with all affirmative action requirements for protected veterans and individuals with disabilities. #J-18808-Ljbffr

You will work closely with experimentalists and engineers to ensure data integrity for robust modeling activities.

Senior Lead, Principal Data Scientist / Associate Director - Data Science. Work closely with cross‑functional teams, including data scientists, data engineers, product managers, and business experts to ensure smooth development of RGM models and translate outcomes to business stakeholders. Princip

MSD Malaysia is looking for a Senior Specialist in Data Science for their Clinical Data Science Realization Team in Rahway, NJ. This role combines hands-on data science delivery with stakeholder interaction, requiring expertise in Python and machine learning.

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing your opi

Follow procedural instructions to ensure data accuracy and reliability.

We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies.Earn up to $750 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing y

Data analysis and reporting tools (SQL, Power BI, Tableau). Experience with financial platforms or data sources (Bloomberg, FactSet, etc.

Design non‑interventional and data synthesis studies; author study protocols, develop questionnaires, case report forms, data analysis plans, final reports, scientific presentations, and publications. Under the guidance of a senior leader, this individual will support the V&I Outcomes Research tea

TBG | The Bachrach Group is seeking a Project Manager in Maplewood, New Jersey, to oversee civil construction projects from preconstruction through closeout.This role is high-impact within a well-established firm known for delivering complex projects on time and on budget.The ideal candidate will ma

Job Overview The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new medicines in the Oncology Asset therapeutic area. Required Experience and Skills Experience in industry or as senior faculty in aca

Stevens Institute of Technology is seeking a Research Scientist in Hoboken, NJ.

We are seeking an experienced Senior Software Business Analyst to support the delivery of business-critical software solutions.

Analyzing data and forecasting usage will be key components of this role. Onboarding New Retail Items: Manage data and publish items for new retail products using systems like One World Sync. Data Analysis: Draft and submit accurate forecasts for wholesalers finished products for key grocery retail

Domain Knowledge: Solid understanding of Wealth Management Operations processes, including areas like trade processing, settlements, reconciliations, client reporting, reference data, and exception management.

Project Manager – Automated Storage & Retrieval Systems.JBAndrews is partnered exclusively with a leading engineering and manufacturing business specialising in high-bay warehouse (HBW) and ASRS solutions, supporting major customers across cold chain, manufacturing, and retail sectors.Due to conti

EVOS Construction Turnkey, a division of All Season Global Solutions, is seeking an experienced and driven professional to join our growing team.We specialize in delivering fully integrated, turnkey construction solutions from concept through completion, with a focus on quality, efficiency, and clie

Drive data migration, system integration, testing, and user training activities. Knowledge of system integrations, cloud ERP solutions, and data migration frameworks.

Our growing client in Morris County, NJ is seeking a.Lean/Six Sigma production environment.This role is responsible for delivering projects that enhance capacity, improve equipment reliability, and support long-term operational performance.You will partner closely with internal teams and external ve

Ability to create customer-facing dashboards and data visualizations.

The Senior Project Manager is a senior level position within the field services group of StructureCare. The Senior Project Manager primary responsibilities include:. In addition, the Senior Project Manager will assist with research and development, and other special projects as assigned.

Construction Project Manager - Solar PV.This position will be staffed out of Soltage’s headquarters in Jersey City, New Jersey.This is a hybrid role, which requires on-site attendance at our Jersey City, New Jersey headquarters 3 days per week.Soltage is a leader in the development, financing, and

We are seeking an individual with a strong background in managing.This individual will be responsible for overseeing all aspects of construction projects, including budgeting, subcontractor coordination, permitting, and client communication.Assistant Project Manager or Project Manager Required .De

Advanced SQL skills with the ability to work hands-on with data. Solid understanding of fixed income instruments and related data structures. Experience working in cross-functional, data-intensive environments.

BCI is looking to a fast-learning associate level Business Analyst for a hybrid role with our direct client.Will be a 6 month contract to start.Required to be in the client office located in Jersey City, NJ 2 days a week.You will be involved in traditional BA duties as well as handling some product

Our client is seeking an experienced Senior Environmental Planner / Project Manager to support a broad range of environmental consulting and permitting initiatives across infrastructure, development, and capital improvement projects.

Programming and data visualization skills (e. Proficiency in Excel and some experience working with large datasets is required. Work/Life Resources to help support topics such as parenting, housing, senior care, finances, pets, legal matters, education, emotional and mental health, and career develo

Associate Gifting & Merchandise Project Manager.World Finer Foods is a full-service sales, marketing and distribution company for specialty food and personal care brands.With over $250 million in annual sales, World Finer Foods sells over 35 brands and over 500 products from around the world.Today w