Scientist jobs in New Jersey

Develop, optimize, and qualify/validate molecular and cell-based assays, including multi-parameter flow cytometry, cell phenotyping, functional assays, cytokine assays (ELISA/MSD/Luminex), qPCR/dd PCR, VCN analysis, and related potency methods. Culture and maintain primary human immune cells and engineered cell products; perform isolation, activation, expansion, and transduction/transfection workflows. Independently design, execute, and analyze experiments; document results in ELNs; interpret data and present findings to cross-functional groups. Support tech transfer of analytical methods into manufacturing/QC, including authoring SOPs, protocols, and technical reports. Collaborate cross-functionally to support product characterization, comparability, process development, release testing, stability studies, and assay troubleshooting. Dexian stands at the forefront of Talent + Technology solutions with a presence spanning more than 70 locations worldwide and a team exceeding 10,000 professionals. As one of the largest technology and professional staffing companies and one of the largest minority-owned staffing companies in the United States, Dexian combines over 30 years of industry expertise with cutting-edge technologies to deliver comprehensive global services and support. Dexian connects the right talent and the right technology with the right organizations to deliver trajectory-changing results that help everyone achieve their ambitions and goals. To learn more, please visit ******************** Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.

Onsite in 909 River Road Piscataway, NJ 08854 Monday - Friday, 8am - 4pm (with some flexibility) Reason for request: Lab development, stability, data integration/analysis work JOB DESCRIPTION: Perform appropriate Lab practices and procedures for making product formulation and testing of products. Follow product stability protocols. Maintain, monitor, validate and calibrate lab equipment, as necessary. Prepare reports, collect data analysis, and communicate progress and completion of tests to leadership. Maintain good record keeping habits. Responsibilities include: Lead the development and implementation of new toothpaste formulas for North America - under the hello and Tom's of Maine brands. Be the R&D point of contact for commercial teams for hello and Tom's key innovation. Lead experimental designs to help identity launch formulations and production processes. Make lab and pilot batches of formulations for stability testing and customer sampling. Support Pilot Plant batches by preparing batch sheets, requesting raw materials, pre-weighing materials and batch execution. Support plant trial batches at various North America locations as needed. Manage multiple stability studies at the lab, pilot and plant scale, working with support groups (analytical, flavor, micro, etc) to deliver samples and follow up on results. Create/maintain all required R&D documentation to ensure flawless, high quality commercialization. This may include R&D project timelines, formula databases, tech transfer checklists, proof of claims documents, registration documents, NODs, change control documents and technical justifications. Manage independent projects and collaborate with cross-functional teams, leveraging diverse perspectives to achieve key project goals and influence beyond your network Create and maintain all required documentation under GMP/GLP per FDA/ICH guidelines as required. Validate new raw material suppliers and packaging as required. Maintain a clean and organized working environment. Work on multiple tasks with changing priorities. Make day-to-day recommendations and escalate issues regarding formula development. Stay abreast of supplier and competitor's new developments. Abide by and follow all company standard operating procedures (SOPs) including those for product development, regulatory and safety. Deliver effective presentations of technical data and project status. Required Qualifications Bachelor's or MS Degree in Chemistry, Chemical Engineering, Biochemistry, Food Science or related fields. 4+ years of experience developing and/or implementing consumer products. Experience scaling up formulations from the lab through pilot or manufacturing scale. Technical understanding of related chemistry and science (for example: active deliveries, emulsions, surfactants, rheology, liquid chemistry) Strong knowledge of ingredient chemistry to be able to understand how the interdependencies and interactions of raw material components affect formulation and process performance Able to multi-task and coordinate various simultaneous projects Strong oral and written communication skills Self-motivated but able to work well within a team environment Knowledge of cGMP /GMP and GLP Excellent computer skills (MS Office, Google suite, SAP, etc.) Preferred Qualifications Knowledge of equipment and procedures for making oral care formulations Experience running stability studies for OTC/Drug products Experience & understanding of producing formulations at the manufacturing scale. Experience with claim substantiation. Strong project planning and management experience Knowledge of Regulatory environment in North America and across the globe Knowledge of ICH/FDA guidelines for stability and testing of new drug products Other Required Experience/Qualifications: Previous laboratory experience preferred. Must have hands-on experience with laboratory instruments. Must be able to learn new procedures in a short period of time. Must be able to follow SOPs and obtain reliable and accurate data. Must be able to document data consistently and accurately. Must be able to perform routine tasks daily

Applications & Product Development Senior Scientist: Work directly for a Middlesex County, NJ area company that supplies high quality oils and specialty ingredients to the beverage industry. Seeking a detail-oriented and motivated individual to join our team as an Application and Product Development Senior Scientist specializing in dairy and alternative dairy protein beverage development. As a Senior Scientist, you will play a crucial role developing and implementing innovative protein-based beverages with knowledge and understanding of dairy beverage production equipment and processes. This role requires excellent communication skills to successfully collaborate across multiple departments to deliver results in a team-oriented setting. The Senior Scientist should be able to lead a team of Scientists and Technicians while meeting critical deadlines and delivering superior service to the clients. Essential Duties and Responsibilities: * Own and manage multiple projects developing stable cost-effective consumer products that meet customer expectations & project parameters including processing parameters, ingredient functionality, costs, regulatory constraints, and flavor tonality. * Formulate new dairy beverage recipes, innovating with new flavors and ingredients, and developing process improvements. * Develop protein beverage formulations from conceptualization to scale-up that meet taste, texture, stability, quality and process optimization. * Be the subject matter expert in training more junior staff. * Conduct routine laboratory tests to resolve technical challenges, ensure products meet performance, stability, quality and safety standards and communicate findings with R&D team and relevant stakeholders, including senior leadership. * Conduct sensory evaluations and prototype evaluations with Applications and Flavor Team to ensure product consistency and quality. * Accountable to monitor and maintain laboratory equipment and supplies, ensuring they are in proper working condition. * Aid in vetting new and alternative ingredients in finished products. * Leverage internal and external resources to bring insight, expertise, and efficiency into project executions and to improve team knowledge. * Scale up lab-scale processes to pilot and production levels. * Ability to travel both domestically and internationally to assist with scale up to support commercialization runs. Education and/or Work Experience and Other Requirements: * Bachelor's Degree in Food Science, Chemistry, or related field. Master's degree preferred. * 8-12 years of experience working as a Scientist in the food and beverage industry. * Strong knowledge of food science principles, regulations, and industry best practices. * Flexibility to adapt to changing priorities and tight deadlines. * Ability to work in a fast-paced and dynamic environment. * Extensive knowledge of food and beverage testing techniques, equipment, and procedures. * Knowledge of Good Manufacturing Practices (GMPs), food safety and quality control procedures. * Excellent analytical, problem-solving, and critical-thinking skills, with keen attention to detail and accurate record keeping. * Effective communication and interpersonal skills with the ability to effectively collaborate with team members and other departments, including outside clients and senior leadership. * Ability to work independently and collaborate in a team environment. Physical Requirements: * Ability to lift and carry objects (up to 50 lbs.) and stand for extended periods of time. Salary: $110-$120k plus benefits and bonus eligible Apply Directly on LinkedIn or through our Website: https://search5.smartsearchonline.com/synerfac/jobs/jobdetails.asp?jo_num=116372&apply=yes&job Title=Applications%20&%20Product%20Development&city Zip=NJ&proximity=25&

Job Title: Scientist I - pharmacovigilance Job Duration: 12 Months Contract - W2 Note: Backfill Onsite role Job Description: As a Scientist in our Post Market Safety & Cosmetovigilance team, your main responsibilities are: • Prioritization of workload for US OTC/Medical Devices (MD) & Hospital visit cases, data entry, MedDRA coding and completion of case narratives of incoming potential Health Related Complaints (HRCs) into the Post-marketing Safety (PMS) database while ensuring completeness and legibility. • Reconciliation of daily cases received from Consumer Care Center (CCC), identify missing cases, correct errors in the Salesforce database & notify CCC manager of discrepancies. • Provide feedback using discretion regarding database issues or with case details that are documented by CCC and communicate database discrepancies. • Support PMS team members with projects regarding completion of cases with missing data or formula numbers as needed and serve as a backup for preparing statistical reports. • Perform data extractions for global PMS analyses and validate data. • Provide ongoing training/feedback of operating tools coordinating with colleagues in France to ensure accuracy. • Provide prompt queries of vendor's database to review all AEs received, notify appropriate partner contacts, review for potential quality-related complaints, notification of manufacturing sites, while maintaining appropriate recording and archiving of information. • Conduct database and data entry training of PMS newcomers within the Americas zone. • Ensure documentation management of departmental work files, including organization of department training documents, Quality Investigations, and maintenance of FDA correspondence. • Review/update standard operating procedures (SOP) and work processes (WP) as needed. • Participate in department presentations to CCC or other métiers. • Ensures compliance with company policies, procedures, and standards. • Ensuring prioritization of data entry workload (OTC/Hospital/MD cases), data exploitation/validation working with colleagues in Global Data Management, ensure department document retention, while working with other Sr. Scientists, Vigilance Coordinators & Head of Post-Marketing Safety. To Succeed in this Position, You Have: • A completed BS or MS in biology or a related field preferred with case processing experience & relevant data exploitation experience in pharmacovigilance. • Minimum of 3-5 years of relevant experience. • Experience in MedDRA coding preferred. • Basic understanding of US Regulations pertaining to Post Marketing Safety preferred. • Knowledge of medical terminology preferred. • Excellent communication (verbal, written) and interpersonal skills required. • Well organized while handling multiple projects simultaneously. • Demonstrated skills in analyzing, reporting, and documenting information with strong attention to detail. • Ability to work independently with minimum supervision in a matrix environment.

6 month contract w/ renewal 3 days onsite in Jersey City, NJ We are seeking a Clinical Scientist Data Reviewer that will support the scientific planning efforts and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate technical skills and scientific acumen as part of a cross-functional clinical development team. You will be a key contributor and supporter in the clinical science activities of evidence generation for regulatory approval and/or engagement with physicians, including protocol development, study implementation, data analysis and reporting of results. This role will be focused on the detailed and critical safety data review efforts from study start-up through final CSR. The Clinical Scientist Data Reviewer is a crucial role in analyzing and interpreting clinical trial data to ensure accuracy, integrity, and compliance with regulatory requirements. There is additional room for growth and leadership opportunities in this role. Responsible for supporting specific aspects of clinical/scientific execution of clinical protocol(s). This may include: Serving as a supportive clinical scientist data reviewer focused on safety, efficacy and critical data deliveries as part of the clinical trial team Supporting the clinical study team as part of the clinical sciences functional line which is closely aligned with the medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with Clinical Research and Pharmacovigilance (as well as other functional areas in this matrix environment) Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); partnering with Clinical Operations on critical and key study deliverables Ensure CRF design supports data collection in alignment with the Protocol in collaboration with Clinical Data Management/Programming Collaborating cross-functionally to review clinical data to ensure quality, completeness, and integrity of trial conduct Potential to provide tactical/scientific mentorship to other clinical scientists and move into Clinical Scientist lead role as well as focus on scientific growth and development Responsible for assisting with the generation, analysis, and presentation of clinical data, including manuscripts, abstracts, and oral presentations (including authoring documents and slide preparation as appropriate) Apply proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; identifies risks and designs mitigation strategies Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs Qualifications 6+ years of experience with a Post Graduate Degree or 8+ years of experience with a Bachelor's degree in a relevant scientific discipline. Experience in clinical drug development experience, or a PhD, Pharm D, or RN degree is preferred. Experience within oncology preferred Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH) Ability to manage multiple competing priorities with good planning, time management and prioritization skills Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions Proficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents related to clinical trials, such as medical monitoring plan, SAPs, informed consent and clinical components of the Clinical Study Reports Interact with key stakeholders across Clinical Development functional areas Role requires proactive approach, strategic thinking and leadership in driving toward clinical study goals Influence opinions and decisions of internal and external customers / vendors, across functional areas Problem solving, prioritization, conflict resolution and critical thinking skills Strong communication, technical writing, and presentation skills experience

The Associate Scientist MSAT Advanced Therapies Validation is responsible for validating supporting processes, implementing improvements within commercial manufacturing, and managing the lifecycle of these processes. The Associate Scientist acts as a Subject Matter Expert for validation studies, particularly in optimizing commercial manufacturing of lentiviral vectors, and liaises with various stakeholder departments. Responsibilities: Contribute to Life Cycle Management (LCM) and New Technology Introduction for the site. Execute validation of supporting processes (e.g.,mixing, sterilization, thermal processing, bio-decontamination). Support the introduction of new technologies and digitalization projects through validation protocol execution. Support the introduction of new materials via execution of validation protocols. Validate process parameters (e.g., process hold times). Contribute to Life Cycle Management projects. Act as Subject Matter Expert for one or more validation categories. Leverage the global MSAT network to identify and implement best practices. Author and review well-documented protocols and reports for all processes to be qualified/validated, in accordance with corporate/site guidelines, procedures, regulatory requirements, and industry best practices. Coordinate and support the execution of validation studies that conform to site standards and client guidelines, while meeting quality requirements. Support the site change control program by performing validation impact assessments and delivering the resulting implementation plan. Investigate deviations associated with process validation activities and oversee pre-validation and validation activities resulting from technical changes. Propose and formalize enhancements to qualification and validation processes and procedures to support process validation throughout the lifecycle and ensure program sustainability. Assist with writing Quality Risk Assessments for existing and new or changed processes. Ensure integration of global standards into local production processes. Support complex investigations and risk assessments. Act as SME during internal and external audits and inspections. Experience: Minimum of 2 years of relevant Manufacturing, Science, & Technology experience in the pharmaceutical industry. Experience with cell therapy manufacturing or viral vector manufacturing. GMP manufacturing and/or validation experience in pharmaceuticals. Skills in communication, planning, documentation, risk management, root cause problem-solving, and knowledge management. Understanding of regulatory requirements and industry guidelines for validation (e.g., FDA, EMA, ICH, ASTM, ISO, ISPE, PDA, etc.). Affinity with process technology and digitalization in manufacturing. Capable of successful delivery of local small projects, regional project work streams, or departmental programs under supervision. Selects applicable engineering/scientific tactics. Works independently within scope, requiring general guidance. Skills: Stem Cell Therapy Good Manufacturing Practices (GMP) Drug Manufacturing Education: BSc in Biochemistry, Biotechnology, Chemical Engineering, or a related field. Advanced degree (MSc/PhD) in Biochemistry, Biotechnology, Chemical Engineering. About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: Azhar Email: **************************** Internal Id: 25-53773

Job Title: Analytical Scientist - Solid Oral Product Development The Analytical Development Department is dedicated to the successful and timely development of new pharmaceutical solid oral products by providing essential analytical development services to clients. The Analytical Scientist will offer analytical support for the team, contributing to the evaluation, development, and validation of analytical methods with limited supervision. The role also involves conducting routine analyses of active pharmaceutical ingredients (APIs) and finished products using advanced laboratory techniques and instrumentation. Specific Duties, Activities, and Responsibilities Perform hands-on method development, improvement, and validation using techniques including, but not limited to: HPLC, GC, Dissolution, UV-Vis Spectroscopy, FTIR, Microscopy, and Particle Size Distribution (PSD). Assist in complex analytical experiments such as unknown impurity identification and excipient compatibility studies. Effectively prioritize activities to provide timely analytical support to product development initiatives. Anticipate analytical challenges in the R&D development process and provide strategic long-term planning for method development and enhancement. Support formulation development and technology transfer activities for assigned projects. Investigate method performance and reliability, and conduct optimization studies as necessary. Collaborate in the preparation of technical documents, including validation protocols and reports, stability protocols and reports, and analytical test procedures. Education and Experience Bachelor's degree (BS) in Chemistry, Biochemistry, or a related discipline with 6-8 years of pharmaceutical industry experience, or Master's degree (MS) in Chemistry, Biochemistry, or a related discipline with 4+ years of pharmaceutical industry experience. Knowledge/Skills Solid working knowledge of GxP principles, regulatory (ICH) guidelines, and compendial (USP/EP/JP) requirements for generic product development.

Vantage Specialty Chemicals is seeking a highly skilled and results-driven Principal Scientist, Complex Fluids & Surfaces to lead a critical enabling platform that advances measurement science and mechanistic understanding across multiple business units. This high-impact senior role will apply fundamental colloid, interface, and surface science to drive technical excellence and deliver differentiated product solutions for consumer and industrial markets, including Personal Care, Food, and Surface Treatment. The Principal Scientist is a recognized technical authority responsible for independently leading, organizing, and executing complex research and development (R&D) projects with broad impact on organizational goals. Operating with substantial autonomy, this individual will develop novel methodologies, guide strategic scientific direction, and serve as the global subject matter expert in complex fluids and surfaces. Key Responsibilities Assume full technical responsibility for the design, execution, and coordination of major R&D projects and initiatives in colloid and surface science. Plan and lead research addressing novel, complex, or controversial scientific problems with significant impact on product portfolios and long-term business strategies. Act as global technical authority in measurement science, establishing worldwide liaison with internal and external experts to shape the company's strategic direction. Develop and apply advanced methods in rheology, interfacial and surface analysis, and particle characterization to provide deep mechanistic understanding of complex fluids and formulated products. Collaborate with R&D, process engineering, scale-up, and operations teams to apply measurement science to both product innovation and manufacturing process improvements. Serve as: Individual Contributor - Lead original, high-impact research, often resulting in new methodologies, inventions, or breakthrough innovations. Staff Specialist - Act as the company-wide expert in applying advanced scientific principles to facilities, products, and technologies. Translate measurement science into consumer-technical models linking physical properties of products with consumer experience and perception. Guide the design, commissioning, and operation of laboratories for advanced instrumentation; ensure scientific instrumentation is maintained, calibrated, and continuously improved. Train, mentor, and supervise junior scientists and technical staff in advanced methods and best practices. Evaluate project outcomes, recommend shifts in strategy, and monitor emerging scientific fields to identify new opportunities. Champion adherence to safety, compliance, and quality standards, while fostering an inclusive and collaborative culture of scientific excellence. Qualifications Ph.D. in Chemistry, Chemical Engineering, Polymer Science, or a related discipline; minimum 5-6 years of relevant industrial R&D experience. Proven track record of technical leadership, innovation, and significant contributions to scientific advancement in complex fluids and surfaces. Extensive hands-on experience with characterization of colloidal and multiphase systems, including viscoelastic surfactant solutions, polymer solutions, emulsions, microemulsions, dispersions, and lamellar liquid crystalline fluids. Expertise in measurement science techniques, with emphasis on rheology for characterizing complex fluids and supporting structure-property and sensory modeling. Familiarity with oscillatory and steady shear methods, viscoelastic behavior, and flow analysis is desirable. Additional experience in tribology, viscometry, surface/interfacial tensiometry, contact angle analysis, foam stability, particle size characterization, and microscopy (PLM, fluorescence, SEM, TEM) is also valued. Strong record of scientific impact through publications, patents, and professional engagement as a subject matter expert. Experience in laboratory design, instrumentation operation, maintenance, and upgrades. Demonstrated ability to mentor and develop junior technical talent. Strong written and verbal communication skills, with experience presenting to technical and business audiences. Authorized to work in the United States.

Title: Bioanalytical Senior Scientist Duration: 12+ months(Extendable) Pay Range: $45 -$53 per hour on W2. NOTES: Must be able to travel between Rahway, NJ site and West Point, PA site as needed. Travel up to 50% may be required. Qualifications: Minimum Educational Requirement: • Ph.D. degree in chemistry, biochemistry or related scientific discipline with 3 years of industrial experience, or Master of Science degree in chemistry, biochemistry or related scientific discipline with at least 7 years of industrial experience, preferably in a bioanalytical laboratory. Required Experience and Skills: • Experience in developing, validating and implementing ligand binding assays under GLP. • Possess excellent written and verbal communication skills. • Experience in Watson or other LIMS systems. • Proficiency with Microsoft Office products. Preferred Experience and Skills: • Highly motivated individual with the aspiration to learn and develop himself/herself. • Experience in LC-MS/MS assay. Responsibilities: Seeking a motivated individual to work as a senior bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a bioanalytical senior scientist position with primary duties in performing laboratory work, preparing reports, and interacting with internal and external partners. This position is a part of the Bioanalytical group, Global Preclinical Development, based in Rahway, New Jersey. Main responsibilities include: • Independently developing, optimizing and troubleshooting LBA methods to support projects with method quality and efficiency in mind; writing bioanalytical methods; assumption of project responsibility in delegated bioanalytical aspects. • Proficiently and independently implementing ligand binding assays (LBA) for the analysis of biological samples in a GLP environment, with duties inclusive of, but not limited to, sample preparation, setting up instruments, processing, and interpreting data; solving issues encountered during method implementation independently. • Establishing LBA capability within the team including equipment purchasing, setting up lab and LBA workflow. • Ensuring that all documentations are in real time, accurate and compliant with current GLP and departmental guidelines. • Preparing reports (sample analysis and validation) independently; Assembling all documents for regulatory submissions; Compliance with and maintenance of required training for company and departmental SOPs, safety-related guidance and other guidelines as relevant/applicable. • Adherence to short term goals, objectives and timelines agreed upon with management, via working independently (e.g., with little to no management oversite in this regard). • Interaction with partners in other functional lines, such as Drug Safety and Metabolism, Quality Assurance, and program management. • Any relevant/applicable additional BA assignments as directed by management. • Ability to multi-task and be a team player.

Job Title: Data Scientist Level 1 Duration: 12 months RTH As a Senior Data Scientist on the GRI Data Science team, you will partner with our diverse team of Engineers, Economists, Computer Scientists, Mathematicians, Physicists, Statisticians, and Actuaries tasked with mining our industry-leading internal data to develop new analytics capabilities for our businesses. The role requires a rare combination of sophisticated analytical expertise, business acumen, strategic mindset, client relationship skills, problem-solving, and a passion for generating business impact. This is an exciting opportunity to be a part of a strategic initiative that is evolving and growing over time! In addition to applied experience, you will bring excellent problem-solving, communication, and teamwork skills, along with agile ways of working, strong business insight, an inclusive leadership demeanor, and a continuous learning focus to all that you do. Here is what you can expect in a typical day: • Responsible for the hands-on development of sophisticated data science solutions comprising the portfolio developed by the Director of Data Science and the technical requirements specified by the Director of Data Science. • Perform hands-on data analysis, model development, model training, model testing, and model deployment. • Continuously research new methods for problem solution, including new algorithms, modeling techniques, and data analytics techniques. • Write production-level code and partner with machine learning engineers to push development code into production. • Partner with machine learning engineers to productionize machine learning models. Partner with data engineers to build data pipelines. Partner with software engineers to integrate solutions with business platforms. • Work closely with the business and data science lead to recommend and develop models for customer engagement and wellness use cases. • Manage external vendors in the execution of the data science development process. The Skills and expertise you bring: • Advanced degree (Master's, Ph.D.) in Mathematics, Statistics, Engineering, Econometrics, Physics, Computer Science, Actuarial, Data Science, or comparable quantitative disciplines. • Working on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results. • Knowledge of business concepts, tools, and processes that are needed for making sound decisions in the context of the company's business. Create and test hypotheses for customer engagement and wellness programs. • Experience in research, designing experiments (ex, A/B testing), working with claims and customer experience data. A behavior science background is preferred but not required. • Ability to learn creative skills and knowledge on an ongoing basis through self-initiative and solving challenges. • Excellent problem-solving, communication, and collaboration skills. Applied experience with several of the following: • Data Acquisition and Transformation: Acquiring data from disparate data sources using API's, SQL, and NoSQL. Transform data using SQL, NoSQL, and Python. Visualizing data using a diverse tool set, including but not limited to Python and R. • Database Management System: Knowledge of how databases are structured and function in order to use them efficiently may include multiple data environments, cloud/AWS, primary and foreign key relationships, table design, database schemas, etc. o Knowledge of how to work with data from (do not build) o SQL skills (relational) - CORE / Initial Proficiency o Unstructured (NoSQL) o Graph/ontology (DB Graph) • Model Deployment: Understanding of: MDLC (Model Development Life Cycle), CI/CD/CT pipelines (using tools like Jenkins, CloudBees, Harness etc.), A/B testing. Pipeline frameworks like MLFlow, AWS SageMaker pipeline, etc. model and data versioning. • Statistics and Computing: Exceptional understanding of: Calculus, Multivariable Calculus, Linear Algebra, Differential Equations, Probability, Statistics, Applied Probability, Applied Statistics, Computer Science (Programming Methodologies), and Cloud. Knowledge of statistical techniques such as the use of descriptive, inferential, Bayesian statistics, time series analysis, etc., to extract business insights and experimentation to solve business problems • Data Wrangling: Preparing data for further analysis; Redefining and mapping raw data to generate insights; Processing of large datasets (structured, unstructured). • Machine Learning: Understanding of machine learning theory, including the mathematics underlying machine learning algorithms. Expertise in the application of machine learning theory to building, training, testing, and monitoring machine learning models. Understanding and expertise in NLP (natural language processing). • Programming Languages: Python, R, SQL, Java or Scala, SQL, Cypher

Title: Data Scientist Duration: Direct Hire Schedule: Hybrid (Mon/Fri WFH, onsite Tues-Thurs) Interview Process: 2 rounds, virtual (2nd/final round is a case study) Salary Range: $95-120k/yr (with benefits) Must haves: 1yr min professional/post-grad Data Scientist experience, and knowledge across areas such as Machine Learning, NLP, LLMs, etc Proficiency in Python and SQL for data manipulation and pipeline development Strong communication skills for stakeholder engagement Bachelor's Degree Plusses Master's Degree Azure experience (and/or other MS tools) Experience working with healthcare data, preferably from Epic Strong skills in data visualization, dashboard design, and interpreting complex datasets Day to Day: We are seeking a Data Scientist to join our clients analytics team. This role focuses on leveraging advanced analytics techniques to drive clinical and business decision-making. You will work with healthcare data to build predictive models, apply machine learning and NLP methods, and optimize data pipelines. The ideal candidate combines strong technical skills with the ability to communicate insights effectively to stakeholders. Key Responsibilities Develop and implement machine learning models for predictive analytics and clinical decision support. Apply NLP and LLM techniques to extract insights from structured and unstructured data. Build and optimize data pipelines using Python and SQL for ETL processes. Preprocess and clean datasets to support analytics initiatives. Collaborate with stakeholders to understand data needs and deliver actionable insights. Interpret complex datasets and provide clear, data-driven recommendations.

Kelly is hiring a QC Analytical Chemist for a 6 -month Contract role with one of our prestigious clients based out in Dayton, NJ 08810. Job Title: QC Analytical Chemist Employment Type: 6-month contract Pay rate: $25-32/hr. Shift: 8 am - 4:30 pm It's an exciting time to be part of Quality Control team. In this position, you will assist with ensuring finished and raw materials are consistent with specifications through analytical testing. As part of the Quality Control department, you will perform wet chemistry analyses based on standard operating procedures as well as sample preparation, data acquisition, data interpretation, and reporting in support of production. You will spend your time… Calibrating and working with analytical equipment daily, including but not limited to: density meter, refractometer, pH meter, titratable acidity, spectrophotometer, moisture analyzer, KF titrator, chlorides titrator Performing tests on finished and raw materials and reporting results Preparing samples, acquiring data, interpreting results Critically thinking and assisting with the investigation of internal and external non-conformances Other duties as assigned Required Skills: Bachelor of Science Degree in Chemistry or Science related field Strong communication skills both written and verbal Knowledge of basic math and science Basic knowledge of computers and Microsoft Office Ability to multitask within the lab to efficiently maintain lab workflow If you believe you are a good fit for this opportunity, please submit your application through the job posting link. We also encourage you to share references if you have them.

Analytical Chemist will be engaged in the different laboratory testing using a range of analytical equipment and techniques within GMP laboratory. MAJOR DUTIES/RESPONSIBILITIES: Perform assigned testing including but not limited to the physical, chemical tests per in-house written procedures and compendial monograph for the raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemistry, physical and instrumental techniques such as LC, GC, UV-Vis Spectrophotometer, dissolution, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments. Document work clearly and perform tests accurately. Record data and results as specified in documentation procedures. Maintain proper laboratory logbooks, notebooks and other records all the time. Report and participate in the deviations and investigations. Comply with all regulatory/in-house requirements (may include but not limited to safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity. · Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by Standard Operating Procedures (SOPs). · Perform laboratory related other duties as assigned. MINIMUM/PREFERRED REQUIREMENTS: Education: Bachelor's Degree in Science/Chemistry Experience: Based on the position level, must require minimum 2-10 years prior experience working in the Quality Control Laboratory in a cGMP environment, preferably in pharmaceutical industry. Hands on Empower-3 experience is plus. QC experience in Generic Pharmaceutical industries would be preferable Knowledge in Good Documentation practices. Knowledge in USP/ FDA BENEFITS: Offers a comprehensive benefits package to employees

RWJBarnabas Health is seeking an experienced and dedicated Chief of Oncologic Quality to lead quality improvement initiatives across our health system's cancer programs. This physician leader will oversee, plan, and execute strategies to elevate patient outcomes, safety, and satisfaction while meeting national benchmarks for excellence. Responsibilities for this role will be split between .3 clinical and .7 administrative and academic involvement - fueled behind a mindset to push the boundaries and build on the improvements that enhance our national rankings, including U.S. News & World Report performance. Responsibilities: Provide leadership in quality improvement, clinical effectiveness, patient safety, and resource optimization across oncology services. Oversee national quality metrics, including U.S. News & World Report rankings and Vizient Oncology Hospital Quality and Accountability (Q&A) Scorecard performance. Implement and monitor initiatives that improve patient care value, outcomes, and operational efficiency across oncology services. Lead a team of direct reports in executing quality initiatives and achieving measurable success. Develop, refine, and support policies, protocols, and programs to enhance patient satisfaction and clinical outcomes. Drive excellence and certification in nationally recognized programs, including: American College of Surgeons (ACS) - Commission on Cancer (CoC) American College of Surgeons (ACS) - National Surgical Quality Improvement Program (NSQIP) American Society for Clinical Oncology (ASCO) - Quality Oncology Practice Initiative (QOPI) American Society for Radiation Oncology (ASTRO) Quality Certification Key Measures of Success: Advancement in national oncology rankings (e.g., U.S. News & World Report). High performance on the Vizient Oncology Q&A Scorecard. Improvement in patient satisfaction scores within oncology medical practices. Achievement of excellence in national oncology quality programs. Qualifications: Board-certified medical or surgical oncologist. Proven leadership experience in quality improvement initiatives. Strong track record in driving metrics-based clinical excellence. Commitment to improving oncology outcomes and patient experience. To learn more about this position, please contact Henry Fishbein, Physician Recruiter, directly via e-mail: ************************ The anticipated salary range for this position if hired to work is $450,000 to $650,000 per year. The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills, and professional experience.

The primary purpose of this position is to prepare samples and perform data collection activities using physics and X-ray based instrumentation at the Transportation Security Laboratory (TSL). Essential Duties & Responsibilities: Performs material characterization (e.g. microscope imaging, density measurements, rheological and mechanical properties). Prepares test samples for analyses Operates explosive detection systems (EDS) as well as analytical physics instrumentation (computed tomography, x-ray fluorescence, x-ray diffraction, etc.) for data collection. Performs troubleshooting, maintenance, and method development on EDS and analytical instrumentation. Safely handles explosive and other hazardous materials. Assembles test articles and bags per test specifications. Develops and uses code (MATLAB, Python, R) for data analysis. Analyzes, compiles, and reports data collection results for research and development and quality control testing events. Composes and reviews technical reports and standard operating procedures. Composes, reviews, and executes test plans. Performs literature reviews. Other duties as assigned. Required Knowledge, Skills and Abilities: Good interpersonal, verbal, and written communication skills. Good listening skills. Good working knowledge of scientific and analytical techniques. Good working skills of software and tools necessary for job functions including Microsoft Office suite, MATLAB, Python. Education/Experience: Incumbent should have a minimum of a bachelor's degree in chemistry, engineering, physics, or other core science and up to five years of experience. Clearance: The ability to obtain a Secret clearance and Department of Homeland Security suitability is required for this position. Supervisory Responsibilities: The incumbent professional has little to no supervisory responsibilities. Working Conditions/Experience: The incumbent is expected to work and/or be available during regular business hours. He/she should also generally be available via e-mail or phone during non-business hours as needed to address critical issues or emergencies. He/she may be required to travel on behalf of the company up to 25%. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions and perform any other related duties, as assigned by their supervisor. Powered by ExactHire:160579

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. Summary: The primary purpose of this position is to contribute to developing, validating, and implementing bioanalytical immunoassays for the measurement of pharmacokinetics (PK), anti-drug antibodies (ADA), and neutralizing antibodies (NAb) in biological samples to support drug development and regulatory filing. Essential Functions: • Develops, validates, and implements immunoassays for the analysis of clinical and non-clinical pharmacokinetic or toxicokinetic samples in a GLP-like or GLP environment with some level of guidance • Ensure assay performance meets regulatory expectations for specificity, sensitivity, precision, accuracy, and robustness. • Independently troubleshoot and optimize ligand binding PK and ADA assays to ensure robustness and reproducibility. • Maintain lab inventories and order lab supplies to ensure continuity of bioanalytical activities. • Utilize Watson LIMS and Electronic Lab Notebooks (ELN) for data processing, documentation, and reporting. • Ensures that electronic notebooks and other documentations are up to date as per departmental guidelines • Prepare or contributes to study reports following the departmental policies and procedures. • Ensures compliance with and maintains required training in BMS and departmental GLP, SOP, safety and other departmental guidelines • Achieves objectives in a manner consistent with the Core BMS Behaviors • Prepares and makes scientific presentations at internal and external meetings Knowledge, Skills, and Abilities: • Strong understanding of GLP-compliant bioanalytical workflows and method development. • In-depth knowledge of global regulatory expectations (FDA, ICH, EMA) for PK and immunogenicity testing. • Skilled in data interpretation and familiar with analytical/statistical software. • Solid foundation in bioanalytical principles including concentration units, calibration curves, and quality controls. • Proficient in laboratory operations: pipetting, balances, and digital tools. • Experience with biological sample handling and automated liquid handling systems (e.g., 96-well format). • Demonstrated expertise in ligand binding assay execution and troubleshooting. • Excellent written and verbal communication skills with a collaborative and solutions-focused mindset. • Strong organizational skills and ability to work effectively in a cross-functional team environment. Education/Experience/ Licenses/Certifications: • Bachelor's degree in relevant life sciences program field • AND 6-8 years of relevant experience Preferred: 4+ years in a CRO or GLP regulated laboratory environment In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Working Environment: Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! **************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Accessibility/Disability Access Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at ***************. Please include your contact information and specific details about your required accommodation to support you during the job application process. *This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

At Bayer we're visionaries, driven to solve the world's toughest challenges and striving for a world where 'Health for all Hunger for none' is no longer a dream, but a real possibility. We're doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining 'impossible'. There are so many reasons to join us. If you're hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there's only one choice. Associate Research Scientist Formulation Development Position Overview: As a Formulation Development Scientist, you will play a crucial role in executing formulation development activities under supervision. You will perform hands-on experiments in the laboratory, including prototyping, material characterization, accelerated stability studies, and initial process design. You will draft formulation development reports and help execute the formulation development strategy for assigned projects. Your role involves solving technical problems by applying scientific knowledge and creative thinking to create simple, cost-effective, and compliant solutions. You will test potential formulations, support laboratory activities, and participate in innovation activities by making prototypes for proposed ideas and concepts. You will contribute to innovation by leading ideations based on category innovation strategy or consumer insights, attending product research to understand consumer feedback, and actively searching for external new drug delivery technologies for new products. You will be instrumental in developing and testing the composition and physical attributes of new products for a stable and process-robust formulation. YOUR TASKS AND RESPONSIBILITIES: * Perform hands-on execution of experiments in the laboratory such as prototyping, material characterization, accelerated stability studies, quality by design - design of experiments execution, initial process design, and drafting formulation development reports; * Help execute formulation development strategy for assigned projects; * Solve technical problems by applying scientific knowledge and creative thinking, creating simple, cost-effective, and compliant solutions; * Clearly identify and escalate formulation issues to supervisor and project team; * Test potential formulations by working with cross-functional project teams to determine experimental and stability test requirements, and reviewing data and conclusions for product testing and stability; * Support laboratory activities as formulation equipment "owner" and subject matter expert, including raw material ordering and naming, and ensuring equipment is in working order; * Participate in innovation activities by making prototypes for proposed ideas and concepts, proactively suggesting new product ideas based on consumer needs or innovation strategy, and actively looking for external technologies and capabilities to apply for internal prototypes; * Contribute to innovation by leading ideations based on category innovation strategy or consumer insights, attending product research to understand consumer feedback on new products, making prototypes against new product ideas, presenting new product ideas and prototypes to category teams, and actively searching for external new drug delivery technologies for new products; * Develop and test the composition and physical attributes of new products for a stable and process-robust formulation; * Contribute to innovation and identify technologies for new product ideas. WHO YOU ARE: Bayer seeks an incumbent who possesses the following: Required Qualifications: * Bachelor's degree; * Ability to work hands-on in a laboratory setting; * Must be passionate about innovation, research, and continuous learning; * Ability to be a fast learner; * Ability to work with cross-functional teams in a rapidly changing environment; * Strong oral and written communication skills; * Experience with design of experiments (DOE) and data analysis; * Ability to work accurately and efficiently on multiple projects under aggressive timelines; * Strong computer and digital skills - Microsoft Office, DOE Software, modeling, and simulation. Preferred Qualifications: * Bachelor's degree in Pharmacy, Chemical Engineering, or Science with 2 years of experience in product development or testing; * Master's degree in Pharmaceutical Sciences, Industrial Pharmacy, Chemical Engineering, or Science with 0-1 years of experience in product development or testing. Employees can expect to be paid a salary between $60,000.00 - $90,000.00. Additional compensation may include a bonus or incentive compensation (if relevant). Additional benefits include health care, vision, dental, retirement, PTO, sick leave, etc.. This salary range is merely an estimate and may vary based on an applicant's location, market data/ranges, an applicant's skills and prior relevant experience, certain degrees and certifications, and other relevant factors. This posting will be available for application until at least December 22, 2025. #LI-US YOUR APPLICATION Bayer offers a wide variety of competitive compensation and benefits programs. If you meet the requirements of this unique opportunity, and want to impact our mission Science for a better life, we encourage you to apply now. Be part of something bigger. Be you. Be Bayer. To all recruitment agencies: Bayer does not accept unsolicited third party resumes. Bayer is an Equal Opportunity Employer/Disabled/Veterans Bayer is committed to providing access and reasonable accommodations in its application process for individuals with disabilities and encourages applicants with disabilities to request any needed accommodation(s) using the contact information below. Bayer is an E-Verify Employer. Location:United States : New Jersey : Morristown Division:Consumer Health Reference Code:858290 Contact Us Email:hrop_*************

Artech Information Systems is the #12 Largest IT Staffing Company in the U.S. and an employer of choice for over 7,000 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US and we welcome you to search the thousands of jobs in our cutting-edge GEM system for employment opportunities that fit your qualifications. At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources. Job Description The incumbent is responsible for, but not limited to the following: • Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies • Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, Client, Investigator Brochure, etc) • Performs literature search and data analysis to address research questions • In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.) • Assisting in database cleaning, review of study results, and interpretation of results • Adhering to key performance indicators for clinical study development, conduct, and reporting • Individual contributor with specialized knowledge • Presents concepts, facts, and reports and advises on key trends and issues • Troubleshooting routine site inquiries • Work is completed under limited supervision • Supports the planning, execution and reporting of clinical programs/trials • May handle multiple protocols simultaneously • Contributes to risk resolution by escalating and monitoring project risks • Minimum of 5-7 years of experience in clinical research in the pharmaceutical industry • A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements • Working knowledge of the IND/NDA/CTD/MAA process acquired through direct industrial experience preferred • Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area; • Bachelor's Required. Doctoral (PharmD or PhD) degree preferred Qualifications BS/MS Additional Information For more information, Please contact Best Regards, Akriti Gupta ************** Morristown, NJ 07960

Clinical Research Scientist Early Development We are seeking a motivated Clinical Research Scientist to join our Clinical Development team and support the execution of innovative clinical studies. This individual will work closely with senior scientists, physicians, and cross-functional partners to contribute scientific expertise, data insights, and clinical input across multiple programs. Key Responsibilities Assist in the design and development of study protocols and protocol amendments. Contribute to the preparation of clinical and regulatory documents, including sections of INDs, study reports, investigator brochures, and updates for health authorities. Provide scientific input into study tools such as case report forms, statistical analysis plans, and data output specifications. Participate in the review and interpretation of clinical safety and efficacy data;support data monitoring activities throughout study conduct. Collaborate with internal study teams and external partners (CROs, vendors, investigators) to ensure high-quality study execution. Present study progress and scientific updates to project leadership and cross-functional committees. Support preparation of data for abstracts, posters, presentations, and manuscripts. Stay informed on evolving therapeutic landscapes, competitive intelligence, and standards of care relevant to assigned programs. Qualifications Advanced degree in a life science discipline preferred (Pharm.D., Ph.D., or equivalent). 1 3 years of experience in clinical research, with at least 1 year in drug development or industry setting. Background in oncology or hematology is a plus. Strong analytical skills and attention to detail, with ability to interpret and communicate complex data. Excellent organizational, written, and verbal communication skills. Ability to work effectively in a fast-paced, collaborative environment and manage multiple priorities. Willingness to travel occasionally (up to ~20%). Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws. By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.