Senior Scientist Jobs in Collingswood, NJ

IFF Health and Biosciences is looking for a Senior Scientist in our Microbiome & Microbiology R&D group. Our IFF laboratories are located within the Experimental Station research site in Wilmington, Delaware. The successful candidate will work with a highly interactive multidisciplinary research team applying rigorous, state of the art science toward the development and discovery of new health products. We are searching for a candidate to join our immune health team who has broad experience working in BSL-2 laboratories and demonstrates conceptual and technical expertise that can be applied to investigations at the intersection of the Mucosal Microbiota and host immune systems. Responsibilities The primary responsibilities of the position will involve technical operations within our tissue culture facility establishing cellular assays using cell lines and primary cells isolated from humans and animals to study host microbiota interaction. In addition to cell culture responsibilities, familiarity with immunological techniques and technologies involved in downstream analysis and the ability to design and develop assays will be required. Most importantly the candidate will need to be team oriented, adaptable, self-motivated, and able to operate within a dynamic professional environment. Desired Skills General lab organization, project planning, and task coordination among team members. Experience with pre-clinical models of host-microbe interaction. Sterile technique and safe handling of samples of human origin. Isolation of Peripheral Blood Mononuclear Cells (PBMCs) from human blood of healthy donors (Buffy coats/leukapheresis paks) Immunoaffinity separations of cells from PBMC preps. (ex: MACS / FACS). Primary immune cell isolation from host tissue and culture techniques. Cell line development by using CRISPR/Cas9. Tissue models; 3D (e.g.Mattek), organoids, co-cultures. Microscopy / immunohistology. Flow cytometry, cytometric bead arrays, Western Blot, ELISA, EliSpot, RNA-Seq. Qualifications PhD in Immunology/Cell biology/mucosal Microbiology or related field. 6+ years of post-PhD laboratory research experience in immunology, cell biology, host-microbe interaction, microbiome-host relationships. 3+ years industrial experience is strongly preferred. Demonstrated knowledge of basic Immunology, cell biology, molecular biology, biochemistry techniques and microbiology, Sterile techniques and experience in the isolation and cultivation of microorganisms, preferably with experience in an anaerobic environment The successful candidate must be motivated, creative, have strong problem solving and critical thinking skills to meet technical objectives and milestones. Excellent written and verbal communication skills and the desire to work as a bench-scientist within a multidisciplinary team are required.

Staff Scientist - Contract - Wilmington, DE Proclinical is seeking a dedicated Staff Scientist specializing in Protein Purification to join our client's team. Primary Responsibilities: The successful candidate will be instrumental in supporting early-stage discovery programs by purifying and qualifying antibody samples. Your work will involve routine maintenance of laboratory equipment and meticulous record-keeping in electronic notebooks. Skills & Requirements: Advanced degree in biology, biochemistry, or a related life sciences field. Proficiency in protein purification techniques. Experience with liquid handling automation is advantageous. Strong organizational, communication, and computer skills. Adaptable and enthusiastic in a dynamic biotech environment. The Staff Scientist's responsibilities will be: Plan, perform, analyze, and document laboratory experiments. Prepare cell supernatants and purify antibody samples. Conduct buffer exchange, quality control, and normalization of purified samples. Troubleshoot and optimize purification workflows for enhanced efficiency. Maintain laboratory instruments and manage supplies. If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.

MasTec Professional Services provides end-to-end engineering, design, and integrated services to the power, oil & gas pipeline, and gas distribution industries across the country. With a genesis in construction and a skilled team of multidiscipline engineers and project management professionals, the company delivers best-in-class infrastructure solutions, including design, asset integrity management, feasibility studies, surveys, constructability reviews, turnkey delivery services, and more. MasTec Professional Services creates collaborative partnerships with clients by building trust and consistently delivering the highest standards of performance. MasTec Professional Services is a purpose-driven company. Our core values guide our strategy, performance, and culture. We believe in maintaining an environment where team members can make an impact, grow, and thrive. A place where they find meaning and purpose in doing the important work of ensuring communities have the vital energy, light, and communications to prosper. Our culture is inclusive and welcoming. Our teams are empowered with abundant training, tools, and opportunities to follow their curiosity and ambitions. Everyone has an equal chance to advance. Everyone is supported, respected, and challenged to be their best. We're always looking for talented and dedicated people to join us and love where they work. MasTec Professional Services is a proud subsidiary of MasTec (NYSE: MTZ), a Fortune 500 Company ranked by Energy News-Record as one of the leading contractors in the country. MPS is part of the MasTec Power Delivery segment. We are certified as a minority-controlled company by the National Minority Suppliers Development Council (NMSDC). Our rich diversity of people and ideas makes us a stronger, more innovative organization. Job Summary We are currently seeking a Part-Time Wetland Delineator/Environmental Scientist/Wetland Specialist/Permitting Specialist who will perform fieldwork for jurisdictional wetland surveys and waters, primarily in the Mid-Atlantic area especially for projects located in Pennsylvania and New Jersey. Candidate must also be willing to learn other aspects of the business which may not necessarily be related to wetland delineations work. The candidate must be located in the areas of Plymouth Meeting, PA, Camden, NJ, or Trenton, NJ. Responsibilities The candidate must be located in the areas of Plymouth Meeting, PA, Camden, NJ, or Trenton, NJ. Perform fieldwork for jurisdictional wetland surveys and waters of the US. Knowledgeable with the Philadelphia, Pittsburgh and Baltimore ACOE region regulatory requirements Provide initial desktop investigations Perform plant identifications, soil analysis and identify hydrological characteristics. Prepare wetland reports summarizing field findings for soil types, vegetation and hydrological characteristics. Provide wetland delineations and flagging. Perform GPS location survey of wetland delineation flagging. Perform preliminary field investigation for evidence of wetlands Perform Joint permit applications. Prepare Requests for Jurisdictional Determination to USACOE as needed. Learn other aspects of the business Qualifications The candidate must be located in the areas of Plymouth Meeting, PA, Camden, NJ, or Trenton, NJ. Minimum 3 years of wetland delineation experience S. or M.S degree in Environmental Science, Environmental Engineering, Biology, Ecology, Botany, Geology or related field Strong knowledge of wetlands and aquatic resources CADD experience a plus Strong technical writing skills Strong organization and time management skills. Able to work under pressure and meet deadlines Certified Professional Wetland Scientist or Delineator preferred but not required. Rutgers University Wetland Training Certification a plus

Hi My name is Gaurav, and I am a recruiter with Net2Source Inc. Our direct client is looking to hire a Scientist - II (Associate) - PA/NJ Only in their growing team. Please find below the job description. Scientist - II (Associate) - Process Development Duration: 12 months Location: West Point, PA 19486 Responsibilities: Seeking candidates for a position within our company's research laboratories Biologics Pilot Plant (BPP) Process Operations Team. This person will work on pilot-scale campaigns for the Good Manufacturing Practice (GMP) manufacture of biologic and vaccine bulk clinical supplies, leading unit operations on either upstream or downstream steps, and contributing to manufacturing activities in the other discipline as needed. A working comprehension of regulatory guidelines governing GMP manufacture is essential. The candidate will work in matrixed teams with process development, facility engineering, quality engineering, GMP compliance, and safety groups. Some overtime, including weekends and occasional second and third shift work, will be required. Assignments include all aspects of preparation, execution, and closeout of a GMP campaign. Primary Responsibilities: • Executing upstream unit operations such as mammalian/yeast/bacterial cell expansion, virus/protein expression in single-use disposable systems and/or stainless-steel bioreactors. • Performing downstream operations such as normal flow filtration, tangential flow filtration, homogenization, lyophilization, chromatography, and centrifugation. • Preparing critical documents including standard operating procedures, batch records. • Completing production readiness activities such as equipment cleaning & steam sanitization. • Evaluating and integrating innovative technology/process equipment fit. • Developing equipment specifications & participating in start-up activities. • Working in a multi-disciplinary project team environment. • Troubleshooting process unit operations. • Leading process unit operation teams. This person will lead manufacturing steps and must be able to plan, communicate, and lead small groups to achieve tactical objectives. Qualifications: • Bachelor's or Master's degree in Chemical Engineering or Biological Sciences with 4-8 years of relevant experience. Required Experience and Skills: • GMP manufacturing and/or process development activities of biologics, or vaccines • Teamwork and collaboration • Working knowledge of cGMP, Quality Systems, and safety for operations • Self-motivated with the ability to work in a fast-paced and dynamic setting Preferred Experience and Skills: • Organizational, problem-solving, and project management skills • Technical background in one or more process unit operations • Experience leading small teams in a matrixed organization Thanks Gaurav Gupta Sr. Pharma Recruiter *************************** **************

Associate Process Scientist - Malvern, PA The Associate Process Scientist will play an essential role in executing laboratory experiments, supporting scale-up activities, and contributing to the safe and efficient development of processes within an API Contract Manufacturing and Development Organization (CMDO). This individual will assist senior scientists and project leaders with process development, safety evaluations, and scale-up efforts while familiarizing with GMP standards. The Associate Process Scientist will also collaborate closely with analytical chemists and contribute to the organization and maintenance of laboratory activities. Responsibilities: Execute laboratory experiments. Assist in determining operational space for various process parameters to ensure efficient and successful scale up. Help evaluate safety of processes utilizing calorimetry data and stability data to fully understand the hazards and the trigger points of these hazards. Follow guidance from senior scientists or project leader to problem solve complex synthetic problems during development. Assist in scale up of processes in the kilo labs. Support scale up of processes in the pilot plant in a GMP environment. Collaborate with analytical chemists to complete work assignments. Contribute to laboratory organization (daily weigh checks, update of lab supplies inventory, lab supply purchase, lab cleaning, equipment calibration). Accurately collect reliable data in the form of lab procedure or reports to be used for updates to customers or during drafting of production's MBR. Qualifications: BS or MS in Organic Chemistry 0-1 years of experience in API manufacturing companies preferred, but not mandatory Knowledge of analytical equipment/instruments such as HPLC, GC, DSC, TGA, KF, NMR, LCMS, and GCMS is preferred. Familiarity with GMP regulations preferred. Good organizational and communication skills required.

5 days in Spring House, PA 1 year contract, high likelihood of extension Our client is looking for an experienced scientist to join the Translational research team within the Oncology Therapeutic Area. This scientist will be responsible for driving functional and molecular testing to support the clinical development of all pipeline projects. The position resides in a highly interactive team, so a collaborative spirit, excellent communication skills (both written and verbal), and strong interpersonal skills are both necessary and highly valued. Responsibilities: Perform plate-based experiments using technologies such as flow cytometer, Incucyte and assay development in cell therapy, to support preclinical work of programs in the portfolio and new targets. Be proficient in multiple cell biology assays that could include cell proliferation, cellular cytotoxicity, immune cell isolation from whole blood, cell culture. Interpret complex data, rework experiments based on interpretations. Troubleshooting, teaching tasks and techniques, correct issues, and provide unsolicited ideas to the team. Prepare clear and concise summaries of their data and present to the project team and senior colleagues. Work in a collaborative environment, being organized, demonstrate urgency and be sensitive to timelines. Communicate results back to the team in meetings, through technical reports, ELN entries, and other means of standard communication. Qualifications: Ph.D or M.S. with 1 years of experience OR BS/BA with 4 years of experience required. Strong cell biology and assay development skills required. Cell/tissue culture with Flow Cytometry/FACS required. Background in Cancer Biology strongly preferred. Prior Biotech/Pharma experience strongly preferred. Preferred: Flow cytometry and imaging flow cytometry (IFC) experience, assay development skills and ability to perform cell functional assays. Cellular and molecular analyses of primary specimens from human donors Knowledge of T cell biology, antigen recognition and metabolism Previous translational research experience in a biotech or pharmaceutical environment

About Us Pace Life Sciences Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP commercial product support. For customers with in-house manufacturing and labs, Pace provides professional services to support their operations. Job Description This is a full-time Formulation Development Scientist I position located in Lebanon, NJ, Monday - Friday, from 8:00 a.m. to 5:00 p.m. SUMMARY Responsible for providing or overseeing the analysis, administration and oversight of comprehensive chemistry/biochemistry policies, programs and practices; may provide feedback and guidance to clients regarding the analysis of materials, products and/or devices utilizing complex to specialized professional and technical knowledge of chemistry/biochemistry/formulation development or related equipment, testing, and procedures. May design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. May interpret analytical data to guide formulation and process development decisions. ESSENTIAL FUNCTIONS Provides complex to specialized analysis in support of various testing materials, products and/or devices utilizing various analytical instrumentation; follows Standard Operating Procedures and methods to perform testing. Provides complex to specialized review, analysis, interpretation, and documentation of testing results. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Provides training and guidance on analytical tests, methods, and instrumentation, as required. Provides complex to specialized analysis, interpretation and counsel to clients, staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves broad operations and leading implementation and change. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients. Assists with developing or participating in chemistry/biochemistry/formulation or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management and/or clients. Develop validate and transfer analytical methods. Provide routine and non-routine analysis using instruments such as HPLC, GC, LC-MS, and FTIR, among others. Design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. Ensure all activities adhere to SOP's, regulatory guidelines, GLP and GMP standards. Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team. Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment. QUALIFICATIONS Education and Experience Bachelor's degree in chemistry/biochemistry, or a closely related field. Two to three (2-3) years of experience, including experience with specialized or technical programs or operations; OR an equivalent combination of education, training, and experience. Required Knowledge and Skills Required Knowledge Complex to specialized principles, practices, and techniques of chemistry/biochemistry and formulation development Broad understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures. Complex to specialized methods to resolve chemistry/biochemistry problems, questions, and concerns. Broad understanding of applicable chemistry/biochemistry laws, codes, and regulations. Understanding of broad testing tools, equipment, and calibration. Computer applications and systems related to the work. Principles and practices to serving as an effective project team member. Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations. Correct business English, including spelling, grammar, and punctuation. Required Skills Performing complex to specialized professional-level chemistry/biochemistry duties in a variety of assigned areas. Overseeing and administering broad and varied chemistry/biochemistry/formulation functions. Ability to operate and train others in analytical instruments and manufacturing equipment. Training others in policies and procedures related to the work. Serving as a team member and the development and management of projects. Operating in a both a team and individual contributor environment. Interpreting, applying, and explaining applicable laws, codes, and regulations. Preparing very complex to specialized functionals reports, correspondence, and other written materials. Using initiative and independent judgment within established department guidelines. Using tact, discretion, and prudence in working with those contacted during the work. Performing effective oral presentations to large and small groups across functional peers and the department. Contributing effectively to the accomplishment of team or work unit goals, objectives and activities. Establishing and maintaining effective working relationships with a variety of individuals contacted in the course of the work. HYSICAL/MENTAL REQUIREMENTS: The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 50 pounds of force occasionally and/or up to 40 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone. WORKING ENVIRONMENT: Work is performed in a lab and office setting. Work is subject to chemicals, fumes, gasses, noxious odors, and related items in a lab setting. Additional Information Benefits 80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance. Equal Opportunity Employer Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Work Schedule Monday through Friday, 8:30 AM - 5:00 PM

Key Responsibilities: Participate in all aspects of the department's visual inspection program, including: Preparing the inspection suite and stocking necessary supplies. Inspecting injectable products and completing related logbooks and batch documentation. Storing finished products according to established protocols. Successfully pass color-blindness and vision testing (must achieve 20/20 with or without correction). Support manufacturing operations when not performing inspections, including: Vial washing, component rinsing, and preparation. Container Closure Integrity testing and other manufacturing tasks. Manage consumables storage and stocking within the department. Perform administrative duties as needed, such as: Revising procedures and templates. Filing and archiving records. Maintaining compliance with cGMP, SOPs, and safety regulations. Identify and communicate business risks to management. Contribute to GMP and safety self-inspection activities. Drive innovation within the Clinical Supply Chain to improve cost efficiency, reduce risk, and enhance service. Monitor and report metrics as required. Ensure zero instances of data falsification or data integrity issues. Utilize basic computer skills, including Word, Outlook, and web navigation.

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 Biology or related fields expert 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.

The candidate will assume a variety of responsibilities in support of the elemental analysis (ICP/ICPMS) and separation MS (GPC/GC/LC/IC) groups within Analytical Sciences Laboratories located in Wilmington, DE. The candidate will work under the direction of technical staff to provide analytical support for R&D, TS&D and Manufacturing as needed. Key job responsibilities include: Preparation of samples, reagents and standards for elemental analysis (ICP/ICPMS) and separation MS (GPC/GC/LC/IC), following a standard procedure (wet chemistry, microwave digestion) Data acquisition and assessing basic data quality Perform routine instrument (ICP/GPC/GC/LC in particular) operation and maintenance Dispose of lab waste and other lab maintenance following a set protocol Cleaning and restocking lab areas as needed Purchases routine lab supplies and reagents Retrieve, move and connect/disconnect cylinders for the purpose of analysis Work safely at all times and ensure a safety culture and a safe working environment in the laboratory. Skills in sample preparation and experience with a variety of lab equipment in a chemical laboratory setting are highly desirable. Hands-on experience with common Elemental Analysis sample preparation methods such as acid digestion including use of HF and open/closed vessel microwave-assisted digestions. Fluent in Microsoft Office software. Prior experience in ICP/ICPMS and GPC/LC/GC/MS is highly preferred but is not a requirement. Prior experience in industrial analytical lab is a plus. An ability to work well with other people under tight timelines and conflicting priorities is critical. Minimum Qualifications: B.S. in chemistry, materials science, physics, or engineering or demonstration of equivalent knowledge acquired in on-the-job training.

Since 1869 we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Michael Angelo's, noosa, Pace, Pacific Foods, Prego, Rao's Homemade, Swanson, and V8. In our Snacks division, we have brands like Cape Cod, Goldfish, Kettle Brand, Lance, Late July, Pepperidge Farm, Snack Factory, and Snyder's of Hanover. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… * Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). * Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. * Campbell's offers unlimited sick time along with paid time off and holiday pay. * If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. * Giving back to the communities where our employees work and live is very important to Campbell's. Our "Campbell's Cares" program matches employee donations and/or volunteer activity up to $1,500 annually. * Campbell's has a variety of Employee Resource Groups (ERGs) to support employees. How you will make history here… The Associate Scientist while be responsible for the coordination and execution of product development and commercialization for Beverage and other shelf stable product initiatives including new platform and line extension innovation, cost optimization, ingredient testing and application, and quality improvements. You will bring a practical application and understanding of food ingredient and technology principles, and the identification and innovative creation of new and unique products that are instrumental in creating food our consumers love, while achieving business goals by ensuring that objectives, product design and timelines are met. You will lead benchtop, pilot plant, and plant trials to test and create prototypes throughout the product development and commercialization process. The Associate Scientist possesses and demonstrates a passion for food innovation, understanding of connection between consumer insights and food product design, ingredient functionality, product and package interaction, low pH shelf stable foods, hot fill and hold process technology, design of experiments, and highly effective communication. You will provide technical leadership in execution of new products and processes in an environment that fosters innovation and calculated risk taking. In this role you will report to the Director of Research and Development. What you will do… * Leads the identification, assessment, and validation of formulations from benchtop through commercialization while partnering with the cross functional team (Marketing, Sensory, Operations/Supply Chain, Engineering, Manufacturing, QA, Regulatory, Process Development and Package Development) and externally with vendors, co-manufacturers, and lab services * Ensures all proper documentation is recorded accurately and project milestones are on schedule. * Conducts and leads assessment and capability studies, product startups/commercialization and provides on-site support to Plant Operations and Quality Assurance for new products, productivity, and quality programs. * Fosters an innovation culture by continually introducing consumer-centric ideas and product concepts for new products, quality improvements, and productivity. Job Complexity: * Conducts and leads prototype assessments with cross functional project teams on an ongoing basis. * Captures feedback and clearly communicates findings and next steps to internal and external stakeholders. * Interact and communicate effectively with Senior Management as well as Plant Management. * Problem-solving skills with ability to identify, interpret and analyze the correct data, and provide detailed direction to development projects * Handles multiple projects concurrently and prioritizes them based on business objectives and timelines with manager's guidance. * Sustains a high level of competence and professionalism in a dynamic business environment. * Demonstrates flexibility and ability to react rapidly to changes in direction. * Demonstrates strong interpersonal skills to work with a team in achieving the targeted results. What you bring to the table… * Required Education: Bachelor of Science in Food science or related field with product development emphasis. * Required Experience: Related experience with a preferred consumer packaged goods background. [Relevant internships or Co-Op programs will be counted toward the experience requirement.] It would be great if you had… * Excellent analytical skills, strong attention to detail, good communication, and interpersonal skills. * Passion for food science, product development, ingredient technology, and consumers as it relates to innovation for new products, line extensions, and productivity opportunities. * Can determine, with guidance, the root cause of a problem and execute effective solutions. * Ability to work with support groups and function effectively in a team environment. * Let your voice shine and be an active participant in the product development process unafraid to share your findings publicly and ask questions on 'why' and 'how'. * Take pride in Campbells iconic brands and products. * Self-starter, able to work independently with a high degree of accuracy in experiments and lab records. * Ability to multi-task and work comfortably in a high-pressure environment. Working Conditions… * Anticipated travel of up to 25% which may include the following: World Headquarters (WHQ) Office, Research Kitchen, Pilot Plant, and Manufacturing Plants (Campbell Soup Company (CSC), co-manufacturers and vendors). * A significant portion of the job is in the thermal production environment; thus, the work exposes the employee to heat and hot food products, coolers, and freezers requiring the use of personal protective equipment. * Ability to walk/stand up at times for up to ¾ of the workday. * Physical ability to handle weights of up to approximately thirty pounds. * Handle allergens including dairy, peanuts, tree nuts, soy, wheat, eggs, and other food ingredient chemicals and allergens while wearing appropriate PPE. * Willingness and ability to taste and evaluate a wide range of food products and ingredients. Compensation and Benefits: The target base salary range for this full-time, salaried position is between $58,700-$84,400 Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package. The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.

Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on the discovery and development of engineered T cell therapies that have the potential to provide a deep and durable, perhaps curative, treatment for patients with autoimmune diseases. The CABA™ platform encompasses two strategies: the CARTA (chimeric antigen receptor T cells for autoimmunity) strategy, with CABA-201, a 4-1BB-containing fully human CD19-CAR T, as the lead product candidate being evaluated in the RESET™ (REstoring SElf-Tolerance) clinical trials in systemic lupus erythematosus, myositis, systemic sclerosis and generalized myasthenia gravis, and the CAART (chimeric autoantibody receptor T cells) strategy, with multiple clinical-stage candidates, including DSG3-CAART for mucosal pemphigus vulgaris and MuSK-CAART for MuSK myasthenia gravis. The expanding CABA™ platform is designed to develop potentially curative therapies that offer deep and durable responses for patients with a broad range of autoimmune diseases. Cabaletta Bio's headquarters and labs are located in Philadelphia, PA. For more information, visit ******************** and follow us on LinkedIn and X (Twitter). Uniquely Differentiated. Rapid. Elegant At Cabaletta, we are driven by the shared mission of developing cures, where a patients' own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew. We're proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work About the Position Reporting to the Senior Scientist, Translational Medicine we are seeking an experienced, motivated, detail-oriented, and highly skilled Senior Research Associate/Associate Scientist within our Translational Medicine team. Under scientific and technical supervision, the individual will be primarily responsible for developing and performing a host of different molecular assays that will support our understanding of Cabaletta Bio's cellular therapies investigated in various clinical trials. More specifically, the candidate will be utilizing Luminex based assays to evaluate serum antibody levels, dPCR to interrogate drug product concentration, and MSD (Meso Scale Discovery) to measure multiple serum biomarkers. As part of the Translational Medicine team, the individual must be able to perform qualified assays on clinical trial participant materials, adhering to internal compliance standards. Responsibilities: With guidance from a Senior Scientist, Translational Medicine, perform translational assays on clinical samples and potentially pre-clinical samples. Perform qualified or validated molecular based assays (Luminex, dPCR, MSD etc.) on clinical samples to inform on cell product persistence, activity, and efficacy in humans. Perform correlative molecular assays with close attention to detail and adhering to tight timelines at certain times. Participate in generating, qualifying, and validating GLP-like assays and author corresponding SOPs, where applicable. Interface heavily with the electronic lab notebook (eLN) system and sample management system; accurately capturing sample metadata and assay data in a timely manner, ensuring data integrity and protocol compliance using an eLN. Maintain GDP-compliant and detailed records for clinical sample lifecycle (receipt, usage, inventory, etc.). Involvement in clinical sample accessioning with close attention to metadata entry. Opportunities to learn and perform cell-based assays such as flow cytometry and cell killing assays. Excellent time-management skills and ability to manage multiple internal projects / workstreams simultaneously. Perform lab associated tasks in accordance with GLP and Cabaletta Bio lab safety policies and SOPs. Have a team-first mentality by maintaining laboratory space and contributing to weekly activities. Qualifications: MS degree in Biology, Immunology, Engineering or related field or Bachelor's degree with 2+ years of experience in an academic laboratory or the biotechnology industry is required. Experience with molecular based assays such as Luminex, dPCR, and/or MSD. Significant lab experience including aseptic technique, mammalian cell culture, human tissue handling, and plated cell-based assays. Must be able to follow SOPs and follow good documentation practices (GDP). Must be highly organized and efficient, able to work independently. Strong problem-solving skills are preferred. Must be able to communicate clearly verbally and in writing. Must have a desire to be part of a growing organization that uses cutting-edge science. Strong team orientation and passion for continuous self-development. Comfortable in a fast-paced small company environment and able to adjust workload based upon changing priorities. Preferred Skills: Experience in protocol design, qualification, and SOP generation. Experience with the Luminex platform. Experience with the MSD platform. Experience with a digital PCR platform. Experience with clinical sample handling and inventory management is highly preferred. Experience troubleshooting, qualifying, or validating molecular based assays. Experience in the biotechnology industry or in a startup industrial setting. Previous experience with GLP/GCP & ICH regulations. Prior use of an electronic laboratory notebook system; involvement in system development is a plus. Our name - Cabaletta - is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression. For more information, please visit https://********************/join-our-crew Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans. Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation. And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm. #LI-ONSITE

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description: • Working within the Prostate/IO drug discovery team to execute in vitro and ex vivo experiments to be used for compound candidate selection and to explore the therapeutic potential of drug targets. • Contribute to development, optimization and troubleshooting of immunological-based assays • Works with minimal supervision on projects of moderate to complex scope • Uses good verbal communication skills and interpersonal skills to communicate with other team members Other duties include data analyses, maintain electronic notebook records of experimental data, summarize and communicate results in internal meetings Must have experience in: • Flow cytometry techniques and flow cytometry analysis. Multicolor flow cytometry experience is strongly desirable.\ • Basic aseptic cell culture technique, such as maintaining cell lines and primary cells, cell banking, etc . • Basic skills in molecular biology including transfection and viral transduction, DNA isolation, cloning, etc . • Experience with cell-based immunoassays, and working with primary cells and ex- vivo analyses is desired . • Familiarity with basic cell purification techniques and immunological phenotyping procedures, as well as processing blood and primary human and rodent tissues, is also desired Demonstrated creativity and Client approaches to solving technical problems • Strong organizational skills including the ability to manage several projects simultaneously • Excellent interpersonal skills with the ability to interact effectively with people, internally and externally Methodical, reliable and comfortable working under fixed timelines Detail-oriented, with excellent record-keeping skills Qualifications Requirements: BA/BS or MA/MS degree in immunology, pharmacology, molecular biology, cancer biology, or related field. 2-5 years of experience (MS/MA) or 2-8 years (BA/BS) years of experience, performing progressively advanced duties at the Associate Scientist I level, or the equivalent training/experience Additional Information Best Regards, Sneha Shrivastava ************

This position is ideal for an early-career machine learning scientist to join the AI & Machine Learning team as a Machine Learning Scientist, supporting photo-based diagnostics and remote treatment monitoring. Partnering with other machine learning specialists and product marketing, you'll provide technical solutions to complex problems in computer vision and 3D data analysis to support Align's product portfolio. This role is key to building out Align's core technology capabilities. * Use data science and machine learning to solve complex, multidisciplinary challenges in applied research and turn technology know-how into execution in a dynamic business environment * Develop algorithms and models in collaboration with business partners, product managers, and software engineers to solve key business initiatives * Design and implement machine learning techniques to improve treatment planning, customer engagement, and device manufacturing based on historical data * Collaborate effectively with other data science teams globally to ensure technology re-use and transfer of new capabilities to drive innovation * Quickly learn and assimilate new business processes, ideas and concepts to formulate conclusions and deliver results. * Identify features and data needed for machine learning solutions. * Help to deliver a vision for our product evolution using machine learning * Stay current on the emerging directions in AI-technologies and support the development of the AI/ML roadmap * Stay current on specific AI-technologies and apply them in an appropriate manner to applicable projects

Responsive recruiter Our mission is to inspire children through science, sparking lifelong imagination and curiosity. For over 25 years, we have delivered unique, hands-on science experiences for children through our after-school programs, birthday parties, workshops, special events, and summer camps. Our innovative programs are as entertaining as they are educational! Mad Science is the world's leading provider of fun science programs for elementary-aged children. As a Mad Scientist, you will lead students through an inquiry-based discovery method involving instructor demonstrations, hands-on activities, and amazing take-home projects that will illustrate how science affects the world around us. Build and fly rockets, demonstrate lasers, explore the states of matter using dry ice, and create slime and other polymers. You will inspire the next generation of scientists through our innovative activities that show kids what science is really about. Responsibilities Facilitate a one-hour after-school science enrichment program using a pre-set curriculum. · Attend orientation and training prior to starting your programs.· Ensure the safety of the kids during programs· Engage with the kids during the activities and experiments. The goal is for the the kids to have fun, not sit through a lecture.· Must be able to lift equipment in kits, can vary in size and weight (heavier kits have wheels). Your vehicle must be able to accommodate the equipment. · Must be able to drive to and from the program with your own vehicle. Programs near you include locations in Haddonfield, Moorestown, and more. Schedule and Pay- You will be scheduled at a school close to you where you will report to at the same day and time each week for either 6 or 8 consecutive weeks. Programs typically start at between 3-3:45PM and last 1.5 hours. - $40 for a 1.5 hour program- Mileage is compensated for any program over 25 miles round trip. Qualifications- Must have experience working with children.- Your own reliable car and license.- Must be over 18 years of age. - Must be vaccinated for COVID-19.- A background in science and/or experiencing performing is a plus! Compensation: $40.00 per hour Mad Science is a powerhouse brand with locations around the globe! For over 35 years, we have sparked imaginative learning through our summer camps, birthday parties, in-class workshops, after-school programs, and special events for kids ages 3-12. Become part of our team and help us inspire the next generation of scientists and engineers. Our locations are always looking for part-time instructors and full-time office staff.

Since 1869 we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Michael Angelo's, noosa, Pace, Pacific Foods, Prego, Rao's Homemade, Swanson, and V8. In our Snacks division, we have brands like Cape Cod, Goldfish, Kettle Brand, Lance, Late July, Pepperidge Farm, Snack Factory, and Snyder's of Hanover. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… * Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). * Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. * Campbell's offers unlimited sick time along with paid time off and holiday pay. * If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. * Giving back to the communities where our employees work and live is very important to Campbell's. Our "Campbell's Cares" program matches employee donations and/or volunteer activity up to $1,500 annually. * Campbell's has a variety of Employee Resource Groups (ERGs) to support employees. How you will make history here… The Associate Scientist while be responsible for the coordination and execution of product development and commercialization for Beverage and other shelf stable product initiatives including new platform and line extension innovation, cost optimization, ingredient testing and application, and quality improvements. You will bring a practical application and understanding of food ingredient and technology principles, and the identification and innovative creation of new and unique products that are instrumental in creating food our consumers love, while achieving business goals by ensuring that objectives, product design and timelines are met. You will lead benchtop, pilot plant, and plant trials to test and create prototypes throughout the product development and commercialization process. The Associate Scientist possesses and demonstrates a passion for food innovation, understanding of connection between consumer insights and food product design, ingredient functionality, product and package interaction, low pH shelf stable foods, hot fill and hold process technology, design of experiments, and highly effective communication. You will provide technical leadership in execution of new products and processes in an environment that fosters innovation and calculated risk taking. In this role you will report to the Director of Research and Development. What you will do… * Leads the identification, assessment, and validation of formulations from benchtop through commercialization while partnering with the cross functional team (Marketing, Sensory, Operations/Supply Chain, Engineering, Manufacturing, QA, Regulatory, Process Development and Package Development) and externally with vendors, co-manufacturers, and lab services * Ensures all proper documentation is recorded accurately and project milestones are on schedule. * Conducts and leads assessment and capability studies, product startups/commercialization and provides on-site support to Plant Operations and Quality Assurance for new products, productivity, and quality programs. * Fosters an innovation culture by continually introducing consumer-centric ideas and product concepts for new products, quality improvements, and productivity. Job Complexity: * Conducts and leads prototype assessments with cross functional project teams on an ongoing basis. * Captures feedback and clearly communicates findings and next steps to internal and external stakeholders. * Interact and communicate effectively with Senior Management as well as Plant Management. * Problem-solving skills with ability to identify, interpret and analyze the correct data, and provide detailed direction to development projects * Handles multiple projects concurrently and prioritizes them based on business objectives and timelines with manager's guidance. * Sustains a high level of competence and professionalism in a dynamic business environment. * Demonstrates flexibility and ability to react rapidly to changes in direction. * Demonstrates strong interpersonal skills to work with a team in achieving the targeted results. What you bring to the table… * Required Education: Bachelor of Science in Food science or related field with product development emphasis. * Required Experience: Related experience with a preferred consumer packaged goods background. [Relevant internships or Co-Op programs will be counted toward the experience requirement.] It would be great if you had… * Excellent analytical skills, strong attention to detail, good communication, and interpersonal skills. * Passion for food science, product development, ingredient technology, and consumers as it relates to innovation for new products, line extensions, and productivity opportunities. * Can determine, with guidance, the root cause of a problem and execute effective solutions. * Ability to work with support groups and function effectively in a team environment. * Let your voice shine and be an active participant in the product development process unafraid to share your findings publicly and ask questions on 'why' and 'how'. * Take pride in Campbells iconic brands and products. * Self-starter, able to work independently with a high degree of accuracy in experiments and lab records. * Ability to multi-task and work comfortably in a high-pressure environment. Working Conditions… * Anticipated travel of up to 25% which may include the following: World Headquarters (WHQ) Office, Research Kitchen, Pilot Plant, and Manufacturing Plants (Campbell Soup Company (CSC), co-manufacturers and vendors). * A significant portion of the job is in the thermal production environment; thus, the work exposes the employee to heat and hot food products, coolers, and freezers requiring the use of personal protective equipment. * Ability to walk/stand up at times for up to ¾ of the workday. * Physical ability to handle weights of up to approximately thirty pounds. * Handle allergens including dairy, peanuts, tree nuts, soy, wheat, eggs, and other food ingredient chemicals and allergens while wearing appropriate PPE. * Willingness and ability to taste and evaluate a wide range of food products and ingredients. Compensation and Benefits: The target base salary range for this full-time, salaried position is between $58,700-$84,400 Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package. The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.

Staff Scientist - Contract - Wilmington, DE Proclinical is seeking a dedicated Staff Scientist to join a dynamic research team focused on preclinical studies in the field of immuno-oncology. Primary Responsibilities: The successful candidate will involve hands-on execution of biological assays and contributing to the development of high-quality therapeutics aimed at addressing inflammatory diseases. This position offers an opportunity to make a significant impact on patient care through innovative research. Skills & Requirements: Degree in Biology or a related field, with a background in Immunology, Biochemistry, Molecular Biology, or Cell Biology. Experience in a research or laboratory setting, with skills in molecular and cellular technologies such as RT-PCR, WB, cell culture, and ELISA. Strong team player with the ability to work independently and manage multiple tasks. Excellent communication skills, both written and oral. Passion for delivering quality medicines and fostering a collaborative scientific environment. Preferred experience in human immunology and/or industry experience, as well as familiarity with multiplex protein and RNA-based technologies. The Staff Scientist's responsibilities will be: Conduct biologically relevant assays to explore mechanistic biology related to inflammatory diseases. Utilize scientific expertise to support ongoing research activities. Generate, review, and discuss complex data sets to drive discovery programs forward. Demonstrate proficiency in cellular and molecular laboratory techniques using advanced technologies. Maintain accurate records of all data generated. Communicate results and their implications effectively to supervisors and peers. Collaborate within a high-performing team while developing independent scientific skills. If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer.

• We are currently seeking a temporary scientist for an immediate onsite position within the Analytical Sciences (AS) laboratory within Science and Technology. • The successful candidate will be expected to perform analytical testing of drug products and APIs under the supervision of a senior scientist. • The candidate will have a good understanding of the technical, regulatory, and GMP needs related to drug product development. • The position will report to the Senior Leadership of the Analytical Sciences laboratory. • Strong technical background with a problem-solving skill set as well as the ability to work in teams are considered essential. Position Responsibilities: • Perform analytical testing (e.g., HPLC/UPLC and dissolution) of drug products • Perform data analysis (chromatography/spectroscopy) and present them to the team in a timely manner Quals-- Education and experience: BS with 4-6 years or MS with 1-3 years or PhD with 0-2 years of relevant experience in Analytical Chemistry. Required Experience and Skills • Hands-on analytical laboratory experience-e.g., wet chemistry, chromatography. • Expertise in Liquid Chromatography (HPLC/UPLC) and dissolution • Hands-on experience with chromatographic integration and with Empower software (or other chromatographic data acquisition systems) and Electronic Laboratory Notebook (ELN) • Experience collecting and analyzing raw data, preparing graphs and other visualization tools to help interpret results • Demonstrated strong verbal as well as written communication skills and ability to work in an interdisciplinary team environment. Key skills: • HPLC and dissolution experience is required. • Analytical chemistry background is required. • Empower expertise is preferred • Pharma industry is preferred Preferred Experience and Skills: • Expertise in UV. • Working knowledge of laboratory GMP, quality, compliance and data integrity requirements and related recent industry trends • Working knowledge of troubleshooting analytical techniques (e.g., chromatography, dissolution, spectroscopy, etc). • Demonstrated ability to work independently in the laboratory • Working knowledge of statistics and tools, e.g., statistical data treatment and/or Excel or Minitab. • Experienced in conducting comparative and or multi-media dissolution studies. Personality: • Collaborative and team player • Independent • Flexible and adaptable Note: 12 months assignment, 100% onsite, lab based role.

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 Biology or related fields expert 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.