Scientist Jobs in West Caldwell, NJ

About the Company - The 6G Wireless Research Center at MediaTek US focusses on research and innovation aiming at creating technological breakthroughs and differentiation in next generation wireless cellular technologies, standards, and future generation of products. By joining the research center you will have the opportunity to invent the future focusing your research on laying the foundation of the revolutionary 6G communication and computing technologies, devices, and systems. About the Role - The applicant must have sustained and demonstrated research accomplishments focused on pushing the frontiers of cutting-edge technologies, development and application of state-of-the-art theory, intelligent algorithms, analytical and simulation tools, as well as Proof of Concept (PoC) demonstrators in the field of modern broadband wireless communication technologies, wireless networking protocols and architectures, and emerging AI/ML techniques. She/he must be able to work with colleagues from various fields in identifying, formulating, and solving new research problems to address the grand challenges of the emerging 6G advanced communications era, which is now in definition mode. The applicant must have a very strong research mindset, possess analytical and exponential thinking, and be driven by the passion for solving unsolved complex problems. The successful candidate will be able to identify, lead and conduct advanced research activities as related to 6G native AI network architecture to address some of the most challenging research problems in the context of 6G paradigm. Furthermore, she/he will be armed with the level of expertise needed to help ensure that MediaTek's future generation products have the desired features to succeed in the marketplace. Qualifications - Ph.D. student who graduated in December 2024 or expects to graduate in 2025 with major in Electrical Engineering, Electrical and Computer Engineering, Computer Science, or related fields Required Skills Significant research experience in industrial and/or academic labs Ability to innovate and create top-quality research assets of prime relevance to 6G native AI network architectures Sustained and demonstrated research accomplishments focused on pushing the frontiers of cutting-edge technologies, development, and application of state-of-the-art theory in the field of modern wireless communication technologies, wireless networking protocols and architectures, and emerging AI/ML techniques Strong innovation track record across multiple wireless generations of technologies, including 4G, 5G and 6G. This includes high quality publications in top journals and conferences, patents, intelligent algorithms, analytical/simulation tools, research PoCs as proof of high-quality research ideas Strong collaborative research skills with industrial and academic partners Strong hands-on expertise (analytical modeling, simulation of complex systems, mathematical analysis, AI/ML systems, algorithm design, building top-quality research PoCs) Strong expertise in evolving wireless networking architectures (sensing, computing, communicating), modern broadband wireless access technologies, AI/ML for cellular, wireless communication systems across layers (from Physical to Application layers), cross-layer protocol design and optimization, security, and privacy Mature research skills in AI/ML, at least in one of the areas related to: Fundamentals of ML, On-Device ML, Privacy Preserving ML, AI for Autonomous Systems, Augmented Reality and Computer Vision, AI for Industrial Intelligence Excellent verbal and written communication skills MediaTek is an Equal Opportunity Employer that is committed to inclusion and diversity to all, regardless of age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (includes pregnancy, childbirth, breastfeeding and related medical conditions), and sexual orientation.

Title: Senior Scientist Work Schedule: Mon -- Fri, Business Hours Duration: 06+ Months Pay rate: $50 - $53/hr on W2 Hybrid role Hybrid = 2 days onsite 1 week, 3 days onsite the next week, subject to change based on the needs of the business. Top Must Have's for candidate to be Considered for this role: Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Summary Report creation/Review in support of CPV (Continuous Process Verification) and APQR (Annual Product Quality Review). Must be detail oriented and proven track record of impeccable time management, to meet timelines. Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. Job Description: The Senior Scientist of Biostatistics is a member of the MSAT team, with focus in CPV (Continued Process Verification) and APQR (Annual Product Quality Review) reporting. Position Summary: The incumbent will support the monitoring/trending of production and release testing parameters, in support of product of personalized cell therapy products for both global commercial and clinical trial supply. The Incumbent will trend CPV parameters, including but not limited to Manufacturing process parameters and Quality Control Release attributes for the MSAT organization, to support the Summit, NJ Cell Therapy facility. The purpose of a CPV program is to provide evidence that a process is running under a state of control. The incumbent will monitor/trend, alerting stakeholders of any drifts and supporting the data reporting of process parameters to the global MSAT organization, while meeting established timelines. The CPV program includes supporting the APQR, as required by regulatory agencies. The incumbent will support the CPV and APQR reports and approvals. The organization being supported is a 24x7x365 manufacturing facility. Work scope will include commercial manufacturing and clinical manufacturing for all cell therapy products manufactured in Summit, NJ Building S12. This role will work with Supply Chain, Manufacturing, Quality Control, Quality Assurance, Project Management, and MSAT. Duties/Responsibilities: Provides support to maintain the site Statistical Process Control (SPC) program, manufacturing performance trending and reporting. Provide multivariate analysis (MVA) modeling for improved process understanding and robustness Continuously monitor CPV parameters, evaluate Statistical Alert Events (SAEs), and take needed actions. Collaborate and support investigations by providing data and analysis Meet CPV and APQR timelines Establish and support predictive process monitoring analytics Supporting any proactive initiatives or investigations related to drift in product performance Represent the site MSAT CPV team in cross-functional forums Performing review and approval of site documents within the scope of CPV and APQR Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness; actively supporting regulatory inspections Interacting with other teams including Operational Excellence, PMO (Project Management Organization), site MSAT, Global MSAT, Quality Assurance, Process Support/Engineering and Manufacturing Support, Manufacturing Operations, Supply Chain Operations Staying current with industry trends and BMS standards and participating in best practice forums consistent with function responsibilities Identify key Opex opportunities, using data driven evaluations Qualifications Specific Knowledge, Skills, Abilities: Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Must be detail oriented and proven track record of impeccable time management, to meet timelines. Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. Expert knowledge of cGMP's and multi-national biopharmaceutical/cell therapy regulations. Experience of facility/clean room design, process, equipment, automation, and validation. Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities. Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies. Experience with Operational Excellence and Lean Manufacturing Education, Experience, Licenses, Certificates: Bachelor's Degree required (science or engineering is preferred); Graduate or higher-level Degree is preferred 8 or more years of work experience in the biopharmaceutical or related Industry 8 or more years of manufacturing support or related experience in the biopharmaceutical industry Experience in CPV and/or APQR reporting preferred. May be substituted for relevant experience in monitoring/trending performance of Quality attributes Experience in cell therapy, biologics, or vaccine manufacturing/support required Experience with Operational Excellence and Lean Manufacturing is a plus

Outlier helps the world's most innovative companies improve their AI models by providing human feedback. Are you an experienced Biology who would like to lend your expertise to train AI models? About the opportunity: Outlier is looking for talented accounting and tax experts to help train generative artificial intelligence models This freelance opportunity is remote and hours are flexible, so you can work whenever is best for you You may contribute your expertise by…Assessing the factuality and relevance of domain-specific text produced by AI models Crafting and answering questions related to BiologyEvaluating and ranking domain-specific responses generated by AI models Examples of desirable expertise:A bachelor's or higher degree in Biology or a related subject Experience working as an Biology professional Ability to write clearly about concepts related to Biology in fluent EnglishPayment:Currently, pay rates for core project work by Biology experts range from $30 to $50 per hour USD. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Triage Staffing is seeking a travel Clinical Lab Scientist (CLS) for a travel job in Newton, New Jersey. Job Description & Requirements Specialty: Clinical Lab Scientist (CLS) Discipline: Allied Health Professional Start Date: 04/07/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours, nights Employment Type: Travel Travel Laboratory: Clinical Laboratory Scientist Newton, NJ Location: Newton, NJ Start Date: 4/7/2025 Shift Details: 8H Nights (12:00 AM-12:00 PM) 40 hours per week Length: 13 WEEKS Apply for specific facility details.Clinical Laboratory Scientist - CA Licensed Triage Staffing Job ID #M99FHYVM. Posted job title: Laboratory: Clinical Laboratory Scientist About Triage Staffing At Triage, we prefer to be real. Real about expectations-both ours and yours. Real about how a decision you make today could affect your tomorrows. Real about how compensation actually works. Real about how great-or grating-your next supervisor may be. Being real allows everyone at Triage to be ready. Ready to serve you with real honesty. So if that gig near the ocean is really no day at the beach, or that third shift comes with a second-class rate, we tell you. So you can be ready, too. We staff all five major divisions of acute care-nursing, lab, radiology, cardiopulmonary and rehab therapy, offering: - Competitive, custom pay packages - One point of contact for both travelers and facilities (per division) - A reliable recruiter who's got your back throughout your entire assignment - In-house compliance and accounting specialists - A clinical liaison team available 24/7 to offer medical and professional support and career development - A mentoring program that is run and managed by actual clinicians-yeah, you read that right - And more (because of course there's more) Are we the biggest? No. Are we the best? That's rather subjective, but we're trying to be. Will we work like hell to get you as close to your idea of heaven as possible? Yes. Yes, we will. Benefits: Day One comprehensive, nationwide insurance plans for health, vision and dental and life-including a HSA option Day One 401(k) program with employer-matching contributions once eligible Facility cancelling protection-your time is money on and off-the-clock Guaranteed hours Weekly paychecks via direct deposit Earned vacation bonuses for time worked Paid holidays Employee assistance program (EAP)-your mental health is important, too Continuing education, certification and licensing reimbursement Workers comp-because accidents happen Top-rated professional liability insurance Company provided housing options Referral bonus-$750 in your pocket after they've completed a 13-week assignment

"All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment". Job Title: Senior Associate Scientist Duration: 12 months Pay rate: $51.97/ hr on W2 Job Description: 4-7 years experience with CAR-T cell therapy Cellular biology techniques, flow cytometry, ELISA Mammalian cell experience Bench level experience, they have to be 100% lab based and looking to stay in the lab. Cell based assays 10+ years CAR-T experience would be overqualified Minimum bachelor's degree with 4+ years experience Comfortable with master's degree with 2+ years' experience About ASK: ASK Consulting is an award-winning technology and professional services recruiting firm servicing Fortune 500 organizations nationally. With 5 nationwide offices, two global delivery centers, and employees in 42 states-ASK Consulting connects people with amazing opportunities ASK Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all associates.

Planet Healthcare is seeking a travel Clinical Lab Scientist (CLS) for a travel job in Newton, New Jersey. Job Description & Requirements Specialty: Clinical Lab Scientist (CLS) Discipline: Allied Health Professional Start Date: 04/07/2025 Duration: 12 weeks 37 hours per week Shift: 7 hours, nights Employment Type: Travel Planet Healthcare Job ID #68210537. Pay package is based on 7 hour shifts and 37 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About Planet Healthcare Delivering Vital Healthcare Talent. Today. Planet Healthcare is a global leader in clinical staffing because we take a candidate-first approach. We pride ourselves on a consultative method and help to create the right opportunity, at the right time, with each healthcare professional. The recruitment engine at Planet Healthcare is driven by leaders in this market, who understand the market demands and trends within your specialty. With a wide array of job opportunities and geographic diversity in our client base, we are your advocate and will work to find the best position for you. We are ready to go to work. Welcome to Planet Healthcare. Our Methodology Let's face it; finding a new job can be scary. Whether you're currently employed or in between positions, the search can feel overwhelming. If you're looking for support, guidance and an upper-hand on the competition, you've come to the right place. We know that not every job, company or commute is right for everyone, so Planet Healthcare recruiters are trained to not only discuss our open job orders, but to find out about your search and take a proactive approach to the market. Our recruiters are experts in this industry and we are your advocate and partner during your job search. We look forward to working with you soon. CLEVELAND | CHICAGO | RALEIGH | BOSTON | PHOENIX Benefits Medical benefits Vision benefits Dental benefits 401k retirement plan Weekly pay Referral bonus

We're seeking an experienced Senior Scientist/Head Chemist with proven expertise in formulation development, troubleshooting, and innovation across skin care, hair care, and body care. In this role, you'll work closely with Marketing, Product Development, and Manufacturing to deliver high-performance, market-ready products that align with consumer trends and business goals. The Role In this role, you will be responsible for: Developing innovative formulations for skin care, hair care, and body care, ensuring technical excellence, consumer appeal, and market relevance. Leading reformulation efforts to optimize product performance, improve stability, and align with regulatory or market needs. Troubleshooting technical issues related to stability, viscosity, pH, compatibility, and texture, delivering solutions that meet quality and performance standards. Collaborating with Marketing and Product Development to translate concepts into viable, on-trend products. Scaling up formulations from bench to pilot and full-scale manufacturing, ensuring process feasibility and consistency. Identifying and integrating new raw materials and technologies to drive product innovation and differentiation. Monitoring stability testing and analyzing results to maintain formula integrity under multiple conditions. Acting as the technical lead in cross-functional projects, bridging communication between R&D, Regulatory, QC, and Manufacturing. Providing mentorship to junior chemists, fostering growth, and promoting lab efficiency. Ensuring formulations meet global regulatory compliance and internal quality standards. Essentials 10+ years of experience in formulation development for skin care, hair care, or body care. Bachelor's degree (or higher) in Chemistry, Chemical Engineering, or related scientific discipline. Expertise in formulating emulsions, serums, creams, gels, cleansers, and treatments with a proven ability to resolve technical challenges. Experience scaling formulations to full-scale production and working with Manufacturing teams. Strong understanding of raw materials and their functionality, with a focus on performance-driven applications. Comprehensive knowledge of global regulatory standards and compliance for beauty and personal care products. Exceptional problem-solving, technical leadership, and project management skills. Proven success working cross-functionally with Marketing, Product Development, and Regulatory teams to bring concepts to market. Excellent technical documentation and communication skills. Preferred not necessary Bilingual English and Spanish

At Quantile Health, our mission is to increase access to transformative medicines. As a Principal Data Scientist, you will play a critical role in shaping our data science strategy, developing advanced analytical models, and driving data-driven decision making across the company. You will work closely with engineering, product, and business teams to design scalable data infrastructure, evaluate foundational models (including LLMs), and translate complex data insights into actionable business strategies. You will be both a hands-on contributor and a strategic leader, responsible for building and deploying high-impact models that solve key business challenges. As the company scales, you will take on leadership responsibilities, including mentoring and growing the data science team. Key Responsibilities Develop, implement, and deploy statistical and machine learning models to solve complex business problems Define and execute the data science roadmap, aligning with business goals and long-term strategy Collaborate with engineering teams to design scalable data infrastructure and optimize data pipelines Evaluate and select foundational models, including large language models, for various business applications Ensure data integrity, accuracy, and quality to drive reliable insights and decision-making Communicate complex findings to technical and non-technical stakeholders, including clients and executive leadership Stay ahead of industry trends, emerging technologies, and best practices in data science Hire, mentor, and develop junior data scientists, fostering a high-performance and collaborative team culture Qualifications PhD or Master's degree in Computer Science, Statistics, Mathematics, Data Science, or a related field 8+ years of experience in data science, with a proven track record of delivering impactful solutions Expertise in statistical modeling, machine learning, and prompt engineering Proficiency in Python and experience working with large-scale datasets Strong understanding of data engineering principles and scalable data infrastructure Excellent problem-solving skills with the ability to translate complex insights into actionable business strategies Strong communication and leadership skills, with experience presenting to executive audiences

We are building a world class systematic data platform which will power the next generation of our systematic portfolio engines. The systematic data group is looking for a Data Scientist to join our growing team. The team consists of content specialists, data scientists, analysts and engineers who are responsible for discovering, maintaining and analyzing sources of alpha for our portfolio managers. This is an opportunity for individuals who are passionate about quantitative investing. The role builds on individual's knowledge and skills in four key areas of quantitative investing: data, statistics, technology and financial markets. Principal Responsibilities Research potential alpha sources, and present to portfolio managers and quantitative analysts Utilize and maintain world-class data processing and transformation engines Build technology tools to acquire and tag datasets Engage with vendors, brokers to understand characteristics of datasets Interact with portfolio managers and quantitative analysts to understand their use cases and recommend datasets to help maximize their profitability Analyze datasets to generate key descriptive statistics Qualifications/Skills Required Ph.D. or Masters in computer science, mathematics, statistics or other field requiring quantitative analysis 3 + years of financial industry experience preferred Programming expertise in Python, C++, Java or C# Programming skills in SQL, PL-SQL or T-SQL Strong problem-solving skills Strong communication skills

Job Title: Environmental Field Technician About Us: A leading international multidisciplinary engineering firm dedicated to delivering innovative solutions across various sectors is looking for a passionate Environmental Scientist. We value growth and seek driven candidates who are eager to make a significant impact. If you are looking to expand your career and work with a standout company, this is the place for you. Join us and enhance your professional journey with a team that supports and values your development. Job Responsibilities: Participate in regular field work, including evenings and weekends as required by project schedules. Assist in coordinating and executing field investigations by logging borings, collecting and managing samples, performing field tests, and recording field data. Observe remediation and construction activities, ensuring compliance with construction documents, remedial work plans, and health and safety plans. Identify and communicate any issues encountered on project sites to supervisors, implement solutions to both routine and complex field problems, and accurately document results. Prepare and manage standard logs and field forms documenting field investigations, including drilling logs, field investigation forms, chain of custody logs, and remedial activities (such as air monitoring data, daily reports, and maps). Conduct file reviews, site reconnaissance, and document searches. Assist with report preparation. Perform other duties as requested. Qualifications: Bachelor's degree in Environmental Engineering, Civil Engineering with an environmental concentration, Environmental Science, Geology, or a related field. 2 to 5 years of relevant work experience. Strong technical education, professional demeanor, and a desire to learn. Excellent written and verbal communication skills. Strong attention to detail with excellent analytical, multitasking, data management, and judgment capabilities. Ability to work effectively both independently and in a team environment. Willingness to spend the majority of work hours in the field. Experience in coordinating field investigations and oversight. Familiarity with relevant investigation and remediation regulations and programs. Valid driver's license in good standing and reliable transportation for access to remote job site locations. Ability to travel to job sites as needed. Availability to work overtime as required.

The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue?our mission?at MSK and around the globe. Job Description: The Organic Synthesis Core Facility at Memorial Sloan Kettering Cancer Center is urgently looking for a PhD-level Organic/Medicinal Chemist to join our team. OSCF supports the work of both clinical and basic science colleagues by addressing their chemistry needs. The successful candidate will be responsible for maintaining high level productivity in the lab and will require good working knowledge of contemporary organic synthesis and medicinal chemistry to support a wide range of research projects. The candidate will have the ability to independently conceive and plan efficient synthetic strategies and designing molecules. The role requires performing experiments within established timelines, and make every effort to purify and characterize products, along with maintaining detailed and accurate laboratory notebooks. Additionally, the candidate will have the ability to reconcile bench work and effectively communicate research findings through written reports, and drafting manuscripts and patent applications. The ideal candidate should have PhD in Organic or Medicinal Chemistry. Excellent oral and written communication skills. Independent problem solving skills. Team spirit and strong interpersonal skills. Experience running flow chemistry is highly preferred. Experience with nucleoside and nucleotide chemistry is desirable. Knowledge of bioconjugation techniques is a plus. This position offers a unique opportunity in a collaborative and fast-paced environment. If you thrive in a team-oriented yet independent role, we encourage you to apply. Application Instructions Interested applicants should submit a cover letter, CV, an abridged overview of your accomplished synthesis or medicinal chemistry work, along with the names and contact information of at least three professional references. Please include specific examples that demonstrate your ability to work effectively in a team, as well as instances where you have shown independent problem-solving skills. Applications should be sent via email to: ******************* Additional Information Hours: Onsite Monday - Friday, 9am - 5 pm Pay Range: $62,985 - $110,000 Closing: MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sexual orientation, national origin, age, religion, creed, disability, veteran status or any other factor which cannot lawfully be used as a basis for an employment decision. Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.

Support of analytical testing and chromatography data collection on samples from small molecule development/characterization. Other activities include method screening, and optimization using liquid chromatography modelling software. Qualifications BS (2+ yrs) or MS/PHD (1+ yr) of relevant experience in analytical chemistry or small molecule testing lab. Industry experience preferred. Required Skills and Experience Must have separations experience for small molecules Experience in analyzing small molecule formulation development samples and/or other therapeutic modalities using at least one of the following techniques: Liquid Chromatography (HPLC / UPLC) Such as: Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX, AEX, CEX), Reverse Phase (RP), or Hydrophobic interaction chromatography (HIC) Spectroscopic techniques (UV, Mass Spectrometry) Desired Skills and Experience General knowledge of analytical chemistry Making accurate reagent preparations (dilutions / solutions / buffers / mobile phases) Good documentation practices & utilization in electronic lab notebooks (ELN) Analytical software including Empower and/or ChemStation or OpenLab Familiarity with Microsoft Office Applications (Outlook, Excel, Word, PowerPoint, OneNote, Teams, etc.) Knowledge of ACD Labs tools such as LC-SIM or any computer coding language is a plus Responsibilities Analysis of analytical samples. Results processing and documentation by following appropriate methods / protocols / procedures Sample & data management following best practices Following all appropriate laboratory safety and hygiene procedures

RESPONSIBILITIES: Responsible for developing and optimizing fit-for-purpose analytical methodologies across early through late stage product development for injectable and ophthalmic drug products. Responsible for designing and executing appropriate pre-validation and/or validation studies required to support analytical methodologies. Must test various samples in support of formulation development, subsequently followed by interpretation of results to provide meaningful guidance to the team. Must verify co-workers calculations in notebooks/logbooks and verifies results in reports and/or appropriate systems to check for accuracy and integrity of data. Required to maintain and clean laboratory instruments and equipment. Required to design and/or execute departmental methods, protocols and SOPs Must perform other laboratory related miscellaneous duties as required. QUALIFICATIONS: A M.S. degree in Analytical Chemistry or related field with 7+ years of experience or a Bachelor's degree with 9+ years of experience 3 - 4 years minimum experience supporting Analytical R&D in regulated industry, familiarity with ICH Guidelines, and world pharmacopeias (USP, EP) are preferred

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. About the role We are seeking a talented and dedicated Scientist to join our team. The successful candidate will be responsible for developing and preparing beverage formulations, syrups, or beverage concentrates at lab and pilot plant scale, following direct customer specifications. Key responsibilities Develop and prepare beverage formulations, syrups, or beverage concentrates at lab and pilot plant scale. Test and establish beverage formulations according to specific taste profiles and regulatory requirements. Customize beverage ingredients independently or within a cross-functional team environment. Calculate calories and understand sweeteners and nutrients in formulations. Facilitate the shipment of samples for internal and external customers. Support beverage and taste development under proper GMPs and safety standards. Maintain flexibility to meet deadlines and handle multiple tasks with speed and high accuracy. Master beverage formulation for sparkling, still, juice and functional beverages. Exceptional sensory skills to define and discriminate flavor profiles in short timelines. Ability to work on RTD and RTM formats at different concentration levels. Deep understanding of beverage processing techniques and nutritional value calculations. Good communication skills to explain formulations at a commercial setting with customers. Good mathematical skills to work with dilutions, percentages and ppm on ingredients. Self- motivated to find a solution to complex problems. Qualifications and skills Degree on Food Technology, Biology, Chemistry, or a related Applied Science. Scientific and analytical aptitudes. Basic computer and mathematical skills. Prior CPG or flavor application experience is preferred. The typical hiring range for this role is $73,758 to $108,755 annually and is based on several factors including but not limited to education, work experience, certifications, location, etc. In addition to your pay, Kerry offers benefits such as a comprehensive benefits package, incentive and recognition programs, equity stock purchase and retirement contribution (all benefits and incentives are subject to eligibility requirements. Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at: Know Your Rights: Workplace Discrimination is Illegal (dol.gov). Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a “starter kit,” investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.

81828 **Please ONLY local candidates to Summit NJ with extensive Pharmaceutical and Manufacturing experience. Experience in cell therapy, biologics, or vaccine manufacturing/support required. TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading pharmaceutical company is hiring a Senior Scientist for a contracting role. Location: Summit NJ MUST have Required skills: Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. Summary Report creation/Review in support of CPV (Continuous Process Verification) and APQR (Annual Product Quality Review) Expert knowledge of cGMP's and multi-national biopharmaceutical/celltherapy regulations Experience of facility/clean room design, process, equipment, automation,and validation Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies Experience with Operational Excellence and Lean Manufacturing Bachelor's Degree required (science or engineering is preferred); Graduateor higher-level Degree is preferred 8 or more years of work experience in the biopharmaceutical Experience in CPV and/or APQR reporting preferred Pay: $51-52/hour W2 Responsibilities: Focus in CPV (Continued Process Verification) and APQR (Annual Product Quality Review) reporting Will support the monitoring/trending of production and release testing parameters, in support of product of personalized cell therapy products for both global commercial and clinical trial supply Will trend CPV parameters, including but not limited to Manufacturing process parameters and Quality Control Release attributes The purpose of a CPV program is to provide evidence that a process is running under a state of control The CPV program includes supporting the APQR, as required by regulatory agencies Travel up to 10% of time may be required within US Provides support to maintain the site Statistical Process Control (SPC)program, manufacturing performance trending and reporting Provide multivariate analysis (MVA) modeling for improved process understanding and robustness Continuously monitor CPV parameters, evaluate Statistical Alert Events (SAEs), and take needed actions

Work Schedule: Mon -- Fri, Business Hours Hybrid = 2 days onsite 1 week, 3 days onsite the next week, subject to change based on the needs of the business. The Senior Scientist of Biostatistics is a member of the MSAT team, with focus in CPV (Continued Process Verification) and APQR (Annual Product Quality Review) reporting. Position Summary: The incumbent will support the monitoring/trending of production and release testing parameters, in support of product of personalized cell therapy products for both global commercial and clinical trial supply. The Incumbent will trend CPV parameters, including but not limited to Manufacturing process parameters and Quality Control Release attributes for the MSAT organization, to support the Summit, NJ Cell Therapy facility. The purpose of a CPV program is to provide evidence that a process is running under a state of control. The incumbent will monitor/trend, alerting stakeholders of any drifts and supporting the data reporting of process parameters to the global MSAT organization, while meeting established timelines. The CPV program includes supporting the APQR, as required by regulatory agencies. The incumbent will support the CPV and APQR reports and approvals. The organization being supported is a 24x7x365 manufacturing facility. Work scope will include commercial manufacturing and clinical manufacturing for all cell therapy products manufactured in Summit, NJ. This role will work with Supply Chain, Manufacturing, Quality Control, Quality Assurance, Project Management, and MSAT. This position is based in Summit, NJ. Travel up to 10% of time may be required within US. Duties/Responsibilities: • Provides support to maintain the site Statistical Process Control (SPC) program, manufacturing performance trending and reporting. • Provide multivariate analysis (MVA) modeling for improved process understanding and robustness • Continuously monitor CPV parameters, evaluate Statistical Alert Events (SAEs), and take needed actions. • Collaborate and support investigations by providing data and analysis • Meet CPV and APQR timelines • Establish and support predictive process monitoring analytics • Supporting any proactive initiatives or investigations related to drift in product performance • Represent the site MSAT CPV team in cross-functional forums • Performing review and approval of site documents within the scope of CPV and APQR • Ensuring safe and compliant cGMP operations and maintaining permanent inspection readiness; actively supporting regulatory inspections • Interacting with other teams including Operational Excellence, PMO (Project Management Organization), site MSAT, Global MSAT, Quality Assurance, Process Support/Engineering and Manufacturing Support, Manufacturing Operations, Supply Chain Operations • Staying current with industry trends and client standards and participating in best practice forums consistent with function responsibilities • Identify key Opex opportunities, using data driven evaluations Working conditions: • The incumbent will be required to adhere to the current client policies and procedures. • The incumbent will be required to gown to access classified manufacturing areas when needed. • This is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job. • This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management. Qualifications Specific Knowledge, Skills, Abilities: • Excellent knowledge of evaluating data using statistics and statistical tools, to make data driven decisions. • Proficiency in major statistical software packages and programming languages (e.g., R, JMP, MINITAB, or SAS). JMP software preferred. • Must be detail oriented and proven track record of impeccable time management, to meet timelines. • Possess strong verbal/written communication skills to enable working with internal/external parties and/or collaborating with cross-functional teams. • Expert knowledge of cGMP's and multi-national biopharmaceutical/cell therapy regulations. • Experience of facility/clean room design, process, equipment, automation, and validation. • Experience with the start-up, validation, and licensure of new biopharmaceutical manufacturing facilities. • Hands-on experience with single-use technologies, closed systems, and cold chain/cryogenic technologies. • Experience with Operational Excellence and Lean Manufacturing Education, Experience, Licenses, Certificates: • Bachelor's Degree required (science or engineering is preferred); Graduate or higher-level Degree is preferred • 8 or more years of work experience in the biopharmaceutical or related industry • 8 or more years of manufacturing support or related experience in the biopharmaceutical industry • Experience in CPV and/or APQR reporting preferred. May be substituted for relevant experience in monitoring/trending performance of Quality attributes • Experience in cell therapy, biologics, or vaccine manufacturing/support required • Experience with Operational Excellence and Lean Manufacturing is a plus

Full-time position Competitive compensation (Salary, Benefits & Options) 180 Varick Street, New York, and 430 E 29th Street, New York Waypoint Bio is a venture-backed biotech startup building the next generation of cell therapies for solid tumors and autoimmune diseases. Traditional cell therapy development faces a trade-off between in vitro approaches that are fast but inaccurate, and in vivo approaches that are accurate but slow and expensive. Using our proprietary platform combining spatial biology, pooled screening, in silico protein engineering, and machine learning, we can obtain both depth and breadth when screening cell therapy candidates - speed without compromising on in vivo accuracy. Our team is highly collaborative, interdisciplinary, and shares the mission of developing novel immune cell therapies to benefit patients' lives. Position Summary: We are seeking a highly motivated, creative scientist who thrives in a fast-paced and collaborative environment. The ideal candidate will have extensive expertise in immunology, including a deep understanding of either regulatory T cells (Tregs) or the design of engineered T cell therapies (e.g. CAR-Treg, CAR-T, TCR-T, or others). Their primary tasks will be to apply their knowledge of the immune system to design novel T cell therapies, optimize the manufacturing of these cell therapies using multiplexed cloning and T isolation & genetic engineering approaches, and then test their function using in vitro and in vivo models of diseases. In this role, you will work collaboratively with our team of computational and wet-lab scientists to develop cutting-edge technologies and new therapeutic options for patients. Duties and Responsibilities Apply your knowledge of immune-related signaling pathways & protein domains to improve the efficacy of existing T cell therapies. Generate hundreds of innovative designs for cell therapies that address the challenges in different disease indications, with a focus autoimmune diseases and solid tumors. Work independently to optimize the manufacturing conditions for Treg and CAR T cell therapies, and implement these strategies to generate libraries of T cell therapies. Develop in vitro assays and in vivo models of Treg function, and work collaboratively to implement these assays to compare the function of different Treg cell therapy designs. Implement existing strategies for highly multiplexed cloning, using either pooled cloning or arrayed cloning approaches. Introduce new technologies and improve the performance, throughput, and accuracy of existing assays Actively engage in prioritizing key milestones and developing appropriate timelines Provide conceptual input on experimental design and interpretation in a team setting Required Qualifications Ph.D. in Immunology, Cancer Biology, Protein Design, Cell Biology, or a related field. Alternatively, M.S. or B.S. degree with 5 years or 7 years of equivalent experience, respectively. 4+ years of academic or industry experience working on immunology and T cell biology. Experience culturing T cells ex vivo and using these cells for downstream assays. Strong molecular biology skills for cloning (e.g. Gibson Assembly) and genetic engineering of mammalian cells (e.g. viral approaches, CRISPR systems). Knowledge of the interplay between the immune system and either healthy tissues or the tumor microenvironment. Practical knowledge of the immune cell therapy field. An excellent scientific track record with published papers or recent experience in immunology or cell therapy. Superb written and oral communication skills, and the organizational abilities to pursue several projects on tight timelines. Preferred Qualifications Deep expertise in the design and testing of engineered Treg cell therapies (e.g. CAR-Treg, armored T cell therapies) for autoimmune and inflammatory indications. Knowledge of the mechanisms used by Treg cells to dampen immune responses in a variety of tissue contexts. Experience designing novel in vitro assays or animal models for autoimmune and inflammatory indications. Send CV and cover letter to apply: ********************

We are looking for an Associate Clinical Research Scientist for a top beauty company hybrid out of their Edison NJ research center! The Associate Clinical Research Scientist plays a key role in organizing and executing clinical studies, under the direction of the Manager of TPS. This role involves working with cross-functional teams, ensuring document integrity and timely communication. The TPS team will provide real-time training of all relevant tasks. Responsibilities: Under the direction of the Manager and VP of TPS, will coordinate clinical studies, ensuring that the goals of the project and timelines are met Ensure studies comply with Good Clinical Practices Recruit and screen new panelists, ensuring they meet eligibility requirements; this may include the preparation and execution of screening surveys to identify qualified panelists. Prepare reports and presentations summarizing findings Specific Internal Testing Responsibilities: study scheduling, panelist recruitment, conducting basic clinical testing protocols (image capture etc.), data collection and report preparation Specific External Testing Responsibilities: work with external testing vendors to set up clinical studies across all Revlon brands, communicating key study objectives, shipment of test samples, review topline data and final reports. Qualifications: AAS in Biological Sciences Required, BS/BA Preferred 1 - 3 years previous relevant experience Strong organizational skills. Evidence of being a good team player. Demonstrated passion, enthusiasm, and flexibility. Ability to multi-task and adapt to change in a fast-paced environment. Ability to work with people from diverse backgrounds. Strong knowledge of Microsoft suite software and a working knowledge of basic statistics Excellent interpersonal and communication skills Provide a positive and professional image of the company through panelist interactions The position involves awareness of confidential panelist data so the candidate must adhere to HIPAA guidelines at all times If you meet the required qualifications and are interested in this role, please apply today. The Solomon Page Distinction Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve. About Solomon Page Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook, and LinkedIn. Opportunity Awaits.

Planet Healthcare is seeking a travel Clinical Lab Scientist (CLS) for a travel job in Hackettstown, New Jersey. Job Description & Requirements Specialty: Clinical Lab Scientist (CLS) Discipline: Allied Health Professional Start Date: 04/07/2025 Duration: 12 weeks 37 hours per week Shift: 7 hours, flexible Employment Type: Travel Planet Healthcare Job ID #68210536. Pay package is based on 7 hour shifts and 37 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About Planet Healthcare Delivering Vital Healthcare Talent. Today. Planet Healthcare is a global leader in clinical staffing because we take a candidate-first approach. We pride ourselves on a consultative method and help to create the right opportunity, at the right time, with each healthcare professional. The recruitment engine at Planet Healthcare is driven by leaders in this market, who understand the market demands and trends within your specialty. With a wide array of job opportunities and geographic diversity in our client base, we are your advocate and will work to find the best position for you. We are ready to go to work. Welcome to Planet Healthcare. Our Methodology Let's face it; finding a new job can be scary. Whether you're currently employed or in between positions, the search can feel overwhelming. If you're looking for support, guidance and an upper-hand on the competition, you've come to the right place. We know that not every job, company or commute is right for everyone, so Planet Healthcare recruiters are trained to not only discuss our open job orders, but to find out about your search and take a proactive approach to the market. Our recruiters are experts in this industry and we are your advocate and partner during your job search. We look forward to working with you soon. CLEVELAND | CHICAGO | RALEIGH | BOSTON | PHOENIX Benefits Medical benefits Vision benefits Dental benefits 401k retirement plan Weekly pay Referral bonus