Scientist jobs in Hamilton, NJ

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

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

Our large pharmaceutical clients is seeking an Associate Scientist to join their growing Biophysics & Molecular Attributes Group in Spring House, PA. The Biophysics & Molecular Attributes Group within Biologics Discovery uses innovative biophysical, biochemical, and mass spectrometry based analytical tools to help select best therapeutic candidates for clinical development. You will be a critical member of the Higher Order Structure (HOS) team that characterizes developability attributes like thermal stability, chemical stability, solubility, and aggregation on a broad range of biologics platforms including monoclonal antibodies, multi-specific antibodies, antibody drug conjugates, antibody radio conjugates, and other therapeutic proteins. You will design and perform experiments using a variety of technologies like HPLC, DSF, DSC, cIEF, GXII, DLS, and more. Key Responsibilities: Execute automated methods for biophysical and structural characterization of antibody therapeutics. Integrate robotic liquid handling systems (e.g., Hamilton, Tecan) with analytical platforms to improve efficiency, consistency, and sample throughput. Execute analytical analysis of biologics candidates using a wide variety of technologies such as size-exclusion HPLC, plate-based HIC/Heparin binding, DSF. Evaluate results to deliver scientifically supported conclusions and recommendations that are documented in appropriate technical reports. Maintain lab and equipment. Collaborate with colleagues in the global organization to support discovery projects. Assist in developing recommendations for improving standard procedures. Qualifications: Master's or Bachelor's Degree in a related field of study Minimum of 1 year of protein/antibody analytical methods experience Experience using HPLC, DSF or DLS Salary: $70,000-$75,000 (flexible based on experience) Hours: Monday-Friday, 8:00am-5:00pm Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year PTO: 10 PTO days, 6 paid sick days annually & paid Holidays Benefits: Medical, Dental, Vision and 401K plans available Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

**1\. Role Overview**Mercor is seeking applied data science professionals to support a strategic analytics initiative with a global enterprise. This contract-based opportunity focuses on extracting insights, building statistical models, and informing business decisions through advanced data science techniques. Freelancers will translate complex datasets into actionable outcomes using tools like Python, SQL, and visualization platforms. This short-term engagement emphasizes experimentation, modeling, and stakeholder communication - distinct from production ML engineering. **2\. Key Responsibilities** ● Translate business questions into data science problems and analytical workflows ● Conduct data wrangling, exploratory analysis, and hypothesis testing ● Develop statistical models and predictive tools for decision support ● Create compelling data visualizations and dashboards for business users ● Present findings and recommendations to non-technical stakeholders **3\. Ideal Qualifications** ● 5+ years of applied data science or analytics experience in business settings ● Proficiency in Python or R (pandas, NumPy, Jupyter) and strong SQL skills ● Experience with data visualization tools (e.g., Tableau, Power BI) ● Solid understanding of statistical modeling, experimentation, and A/B testing ● Strong communication skills for translating technical work into strategic insights **4\. More About the Opportunity** ● Remote ● **Expected commitment: min 30 hours/week ● Project duration: ~6 weeks** **5\. Compensation & Contract Terms** ● $75-100/hour ● Paid weekly via Stripe Connect ● You'll be classified as an independent contractor **6\. Application Process** ● Submit your resume followed by domain expertise interview and short form **7.About Mercor** ● Mercor is a talent marketplace that connects top experts with leading AI labs and research organizations ● Our investors include Benchmark, General Catalyst, Adam D'Angelo, Larry Summers, and Jack Dorsey ● Thousands of professionals across domains like law, creatives, engineering, and research have joined Mercor to work on frontier projects shaping the next era of AI

Chemist - Horsham, PA We are looking for skilled individuals who have knowledge, training and practice the principles of quality on a daily basis. The individual must be hard working and extremely ambitious. They must also have the ability to learn and manage/prioritize responsibilities in a dynamic business environment. The analytical group is responsible for the analysis of raw materials, in-process materials, stability, and finished products in conformance with cGMP regulations. The group is also responsible for the scheduling and calibration and maintenance of equipment. The group also performs method development and validation for various analytical methods. As a member of the team, you will be expected to follow and help plan the daily operations within the lab and communicate with all areas in the company to meet client and company deadlines. Keys to Success and ResponsibilitiesExpertise with analytical instrumentation, HPLC, UHPLC, Dissolution, Spectrophotometer, GC, KF (potentiometric and coulometric), ICP-MS, Viscometers, etc Knowledge and experience of USP, ICH and CFR regulatory requirements Expertise with analytical techniques, Method Development/Validation, chromatography, pipetting, solution preparation, etc Expertise in electronic systems, LIMS, electronic laboratory notebook, TrackWise, OpenLAB, Excel, Word, Authoring monographs, etc Perform various analytical tests, Assay, dissolution, degradants, moisture, hardness, viscosity, pH, etc Execute against monographs, protocols, and SOPs in a cGMP laboratory environment Prevent deviations and investigations The ability to conduct stability scheduling and studies Adhere to deadlines in a changing environment Ability to learn and teach laboratory techniques Schedule work based on priorities and manage time efficiently Perform general laboratory maintenance and cleaning Work collaboratively in cross-functional teams Liaise with customers, staff and suppliers Be aware of, and keep up to date with, health and safety issues Maintain laboratory inventory Prepare documentation for product license applications/regulatory filings Practice continuous improvement Develop business through new quotations, seek new clients, and interact with current clients Responsible for training employees in lab techniques and cGMP procedures Must be a self-starter and capable of working with minimal oversight Create value for the position, department, and company Improve systems and procedures to prevent errors Work in a fast paced and challenging environment Salaried employees are compensated for a 50 hour work week Education & Experience RequirementsMinimum of a Bachelor's Degree in chemistry to an accredited US college or university 3 + years of previous related lab experience

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

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, 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… Imagine...working for a company that knows that its people are the key to its success in the marketplace. A company in which achieving extraordinary results and having a stimulating work experience are part of the same process. We cultivate and embrace a diverse employee population. We recognize that people with diverse backgrounds, experiences and perspectives fuel our growth and enrich our global culture. We are looking for an individual who enjoys working in a fast-paced, team-oriented environment, likes to be challenged, and values the opportunity to make a difference. The Associate Scientist R&D will be responsible for supporting the Research & Development activities on the RTS Soup & Innovation Product Development Team. In this role you will be executing projects across the Soup & Broth portfolio, including ready to serve soup and innovation. The scope of the job encompasses the entire Product Development process from idea conception through plant commercialization. What you will do… * Execute work plans for the Ready to Serve Soup Business supporting one or more projects of low to moderate complexity and technical risk. * Demonstrate organizational and planning skills. * Assist with the development and execution of project timelines, which include contingency planning. * Leverage vendor capabilities to expand formulation possibilities and ingredient solves to increase speed to market. * With guidance, develop prototypes to support concept and ideation exploration work and continue to refine the prototypes based on consumer feedback. * Work on the bench and pilot plant line to understand initial feasibility of new products and conduct ingredient screenings during benchtop evaluation. * Conduct trials in the Pilot Plant and/or manufacturing facilities to assess manufacturing capability and consumer acceptability. * Incorporate nutritional and cost parameters into product design. * Demonstrate flexibility and agility by being able to adapt quickly to changes in direction. * Partner with team members to advance projects and be able to function effectively in a cross-functional team environment. Lead cross-functional tastings with business partners and stakeholders. * Communicate plans, results and project risks to vendors, senior functional staff and/or business teams as required. * Work independently to create new concepts based on research, benchmark and creativity solutions. Who you will work with… In this role you will report to the Manager of Research and Development - Soup & Broth. What you bring to the table… (Must Haves) * Bachelor of Science or higher in Food Science or related field. * Minimum of 6 months in CPG or Foodservice industry or related experience with basic or Co-Op food product development experience. It would be nice if you have… (Preferred Skills) * Demonstrated skills in commercializing products/processes in the manufacturing environment are desired. * Creative problem-solving skills. * Technical, culinary, and new product curiosity for food. * Ability to work with ambiguity and seek creative solutions. * Inclination to work in a team environment. * Strong planning and organizing skills. * Ability to synthesize data, interpret, and provide recommendations. * Highly capable with lab practices, running & improving test methods, material preparation, and batch assessment. * Strong planning and organizational skills. * Good written and oral communication skills. * Basic understanding of consumer testing methodologies. * Computer skills include basic fluency in Microsoft Office, and database management. Working Conditions: * Anticipated travel of up to 30% to locations 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 or 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 $57,800-$83,100 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.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Organization Overview: At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Responsibilities: Lilly Imaging/Avid Radiopharmaceuticals provides technical expertise for molecular imaging to Lilly Research Laboratories. The scientist will provide expertise for biological assay development for the discovery and characterization of novel PET imaging agents, with a focus on neuroscience or oncology imaging and other therapeutic areas. This scientist will work independently, coordinating experimental details of internal and external partnered projects, conducting experiments him/herself, performing data analysis, and presenting data to internal teams and the international scientific community. Establish and execute imaging research projects supporting oncology, neuroscience or other drug discovery and biomarker projects Design and conduct novel binding assays, including radioligand binding assays Characterize and purify biological targets Collaborate with internal project teams, implement translatable imaging biomarker assays and ensure seamless translation of projects Publish results of research projects as appropriate Participate in extramural scientific organizations and attend scientific symposia as well as workshops in order to continue educational/professional development Other duties as assigned Basic Requirements: Degree in physical or biological sciences or imaging-related field Bachelor's degree with min of 15 years' experience, master's with a min of 12 years' experience, or PhD in scientific field. Experience with in vitro assay development Peer-reviewed publications Additional Skills/Preferences: PhD degree preferred Experience in Oncology or Neuroscience, preferably in molecular imaging Experience designing and executing novel biochemical, cellular and tissue assays, including radioligand binding assays (e.g. filtration binding, ELISA/AlphaLISA, SPR and LC/MS) Experience working with amyloidogenic proteins Demonstrated ability to independently conceive, design and execute the characterization and purification of biological targets Experience in drug discovery of PET molecular imaging agents Peer reviewed publications Willingness/desire to learn and incorporate additional technologies or therapeutic area biology to address imaging needs Excellent communication skills (both written and verbal) Excellent presentation skills Strong organizational skills and ability to effectively manage multiple priorities Creativity and critical thinking skills Team Player Additional Information: Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities participate in the workforce and ensure equal opportunity to compete for jobs. If you are an individual with a disability and require a reasonable accommodation to participate in the application process, please email Lilly Recruiting Compliance. Please note, this email address is intended for use only to request a disability accommodation, please email Lilly Recruiting Compliance for further assistance. Inquiries which are not requests for accommodations may not receive a response. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $121,500 - $198,000 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Job Number #170414 - Piscataway, New Jersey, United States Who We Are Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name! Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values-Caring, Inclusive, and Courageous-we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all. Oral Care Research Scientist - Global Product Development This role is for a Research Scientist focused on Global Product Development of innovative and novel Oral Care products. The scientist will be responsible for leading the technical development of new user experiences, creating experimental demonstrations to showcase the products' mode of action, and supporting the successful commercialization of advanced formulas from lab to Technical Readiness. Responsibilities: Product Development & Formulation Lead the development and validation of oral care products such as Toothpaste, Mouthrinses and novel new formats formulas for Global Markets focussed on Freshness offerings and adjacencies. Apply a technical understanding of related chemistry and science (e.g., active deliveries, emulsions, surfactants, rheology, liquid chemistry) to new product innovation. Lead experimental designs to help identify launch formulations and production processes. Make lab and pilot batches of formulations for stability testing and for other validations, such as consumer tests, clinicals and customer samplings. Make day-to-day recommendations and escalate issues regarding formula development. Stay abreast of supplier and competitor's new developments. Testing, Scale-Up, and Documentation Manage multiple stability studies at the lab, pilot, and plant scale, collaborating with support groups (analytical, flavor, micro, etc.) to deliver samples and follow up on results Support Pilot Plant batches by preparing batch sheets, requesting raw materials, pre-weighing materials, and executing batches Create and maintain all required R&D documentation to ensure flawless, high-quality commercialization. Maintain all required documentation under GMP/GLP per FDA/ICH guidelines as required. Documentation may include R&D project timelines, formula databases, tech transfer checklists, proof of claims documents, registration documents, and technical justifications Collaboration and Communication Be the R&D point of contact for commercial teams for their Freshness related projects Manage independent projects and collaborate with cross-functional teams, leveraging diverse perspectives to achieve key project goals. Deliver effective presentations of technical data and project status, including experimental demonstrations of product mode of action. Abide by and follow all company Standard Operating Procedures (SOPs), including those for product development, regulatory, and safety. This role requires a scientist who is self-motivated and able to work well within a team environment, as well as being capable of managing multiple tasks with changing priorities Required Qualifications: A minimum of Bachelor's or MS Degree in Chemistry, Chemical Engineering, Biochemistry, Food Science or related fields. 3+ years of experience developing and/or implementing consumer products. Technical understanding of related chemistry and science (for example: active deliveries, emulsions, surfactants, rheology, liquid chemistry) Strong knowledge of ingredient chemistry to be able to understand how the interdependencies and interactions of raw material components affect formulation and process performance Able to multi-task and coordinate various simultaneous projects Strong oral and written communication skills Self-motivated but able to work well within a team environment Knowledge of cGMP /GMP and GLP Excellent computer skills (MS Office, Google suite, SAP, etc.) Preferred Qualifications Knowledge of equipment and procedures for making oral care formulations Experience running stability studies for OTC/Drug products Strong project planning and management experience Knowledge of Regulatory environment across the globe Knowledge of ICH/FDA guidelines for stability and testing of new drug products Compensation and Benefits Salary Range $83,000.00 - $117,000.00 USD Pay is determined based on experience, qualifications, and location. Salaried employees may also be eligible for discretionary bonuses, profit-sharing, and long-term incentives for Executive-level roles. Benefits: Salaried employees enjoy a comprehensive benefits package, including medical, dental, vision, basic life insurance, paid parental leave, disability coverage, and participation in the 401(k) retirement plan with company matching contributions subject to eligibility requirements. Additional benefits include a minimum of 15 vacation/PTO days (hourly employees receive a minimum of 120 hours) and 13 paid holidays (vacation days are prorated based on the employee's hire date within the calendar year). Paid sick leave is adjusted based on role and location in accordance with local laws. Detailed information regarding paid sick leave entitlements will be provided to employees upon hiring and may be subject to adjustments based on changes in legislation or company policies. Our Commitment to Inclusion Our journey begins with our people-developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business. Equal Opportunity Employer Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law. Reasonable accommodation during the application process is available for persons with disabilities. Please complete this request form should you require accommodation. For additional Colgate terms and conditions, please click here. #LI-On-site

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

R&D Assistant Scientist - In vivo Full-Time position Level: Assistant Scientist Location: On site (Philadelphia, PA) Start date: Available immediately Why Join Verismo? Our team is small but driven, with the single focus of bringing life-changing cell therapies to patients with cancer. With a solid pipeline built around the novel KIR-CAR platform, and two clinical trials underway, our technology has found a way to circumvent the barriers in solid cancer where other CAR therapies have had limited success. KIR-CARs eliminate the artificial recombinant chimeric receptors used in CAR T cells and instead use a natural NK cell derived signaling system. This system is potent against both hematologic and solid tumors, and in preclinical models is superior to current CAR T in conferring long-term, sustained anti-tumor function to overcome T cell exhaustion. We have a strong team for pre-clinical development, CMC with PD and AD, clinical product manufacture, and lead clinical investigators bringing KIR-CARs to patients in need. Our company is comprised of individuals who each bring something unique to the table and are valued for their contributions. Our culture is based on the concept of ‘love what you do' and the dedication that builds a team where people do their best and support one another. Because we believe our people are our greatest asset, career development is an encouraged as an investment in our team and we encourage a healthy work/life balance. Overall Job Purpose: An Assistant Scientist will first and foremost be a people-person, with the necessary scientific background to assist the senior Scientist with conducting scientific studies in the cutting-edge gene-engineered T cell therapy. The candidate will be working closely with our KIR-CAR translational science team in managing daily operations in the laboratory, and assisting with in vivo preclinical studies and ensuring Quality and Data Integrity are preserved in preparation for IND application and transition to first-in-human clinical trials. Additional responsibilities will include assisting with lentivirus preparation, cell line maintenance and related tasks. This role will also be fluent in communicating with our internal scientific team. The candidate will report directly to our Executive Director of Translational Science and assist R&D senior scientists with our in vivo experiments, by preparing materials, designing experiments, acquiring and analyzing data for IND-enabling studies and other translational studies. This individual will help manage daily operations in the laboratory and contribute to studies across R&D functions when needed. The candidate will be a team player who is eager to work in a fast-paced environment. Job summary: Assist R&D scientists with all in vivo experiments including, design, data acquisition, and data analysis to support pre-clinical development of Verismo's pipeline candidates in potential cancer indications. (70%) Manage the daily operation in the Verismo's translational science laboratory, including but not limited to ordering laboratory consumables and reagents, monitoring and maintaining the inventories, maintaining laboratory equipment, following safety procedures, and maintaining compliance records and lab notebooks in an industry setting. (15%) Assist R&D scientists with other lab tasks as assigned (15%). Essential Duties & Responsibilities: General scientific knowledge and laboratory skills. Hands-on lab work in a flexible, fast-paced industry setting is essential. Aseptic cell culture techniques are required. Working knowledge in mouse handling, IV/IP/SubQ injections, and blood and tissue collection is preferred. Experience in problem solving ability and ability to apply risk-based critical thinking in a technical environment. Ability to collaborate across R&D teams and good interpersonal skills. Technical written and oral communication skills are essential. Ability to prioritize, independently manage and complete deliverables within given timelines. Good organizational skills and attention to detail with high quality output. Appropriately document research findings in lab notebooks. Takes responsibility for laboratory efficiency, compliance and cleanliness. Required Qualifications, Experience & Abilities: B.A./B.S. in molecular biology, cell biology or related field with at least 2-3 year research experience. Working experience with cell culture and mice is a must. Molecular biology and flow cytometry experience is preferred. Prior industry experience with adoptive cell therapies is preferred. Prior experience working in a team setting. Well-organized and has experience documenting protocols and recording the data generated from them in an industry setting. Willingness to take other duties as assigned. * Please note that we cannot reimburse travel expenses for candidate interviews.

The Downstream Manufacturing Scientist is a hands-on position responsible for executing purification of mammalian cell-based cultures and producing recombinant proteins for a wide range of mammalian based biosimilars. The candidate will be responsible in the purification of 50L to 1000L volumes engineering, clinical and commercial batches in a cGMP environment. This position requires technical expertise in AKTA purification skids or similar, TFF and knowledge of initiating batch records, protocols, investigations and other technical documents. Work in a team environment to execute batches and can work independently with minimum supervision. This position requires extensive technical expertise in mammalian cell-based purification processes, cGMP manufacturing and compliance for BLA requirements. Essential Duties & Responsibilities Perform downstream process at multiple scales in a cGMP environment, column packing, process troubleshooting and data analysis. Provides technical direction in the execution and development of the purification process. Uses programs to collect and evaluate operating data to conduct on- line adjustments to products, instruments or equipment. Ensure that engineering and clinical batches are executed in a timely manner. Establishes operating equipment specifications and improves manufacturing techniques. Works with other teams and outside vendors to resolve technical issues as well as maintenance of production equipment. Should follow GMP instructions in the manufacturing area and take the lead to follow environmental health and safety policies. Coordinate the conduction of investigations and corrections for issues found during the batch execution process. Performs other functions as required or assigned Complies with all company policies and standards Requirements Education: Requires a Bachelor or Master' degree in chemical, biological or biochemical sciences and a minimum of 4- 5 years of related experience in the biopharmaceutical industry. Previous experience working in GMP and aseptic manufacturing environment. Experience working with AKTA Process skids or similar and familiarity of single use manufacturing consumables such as bags, tube sets, columns and process manifolds. Possess knowledge to execute engineering and clinical batches; familiar with GMP documentation. Special Skills: Ability to work with other team members and independently - good interpersonal skills. Good communication skills: verbal and written, good computer and organization skills, detail oriented. Basic computer skills, including knowledge of Word, Excel and spread sheet Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review. Knowledgeable in cleaning verification/validation. Work Environment & Physical Demands: General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines. Some travel may be involved. Supervisory Responsibility, if any: No This position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.

Job Title: Research Associate Co-op, Cell Culture Process Development Designs, executes and authors upstream cell culture development, optimization, scale up and tech transfer. Collaborates with other internal PD teams during process development and tech transfer. Partner with other internal PD teams during process tech transfer. * Responsibilities * Working on bench scale cell culture process development, optimization and process transfer studies under supervision. Assisting pilot-scale experiments for non-GMP material generation. * Assisting experiment workflow to ensure on time delivery: from initial planning, experiment execution, to data evaluation. * Performing data analysis and interpretation, and assisting in strategies for optimization and troubleshooting. * Performing job specific tasks in compliance with applicable Regulations, International Standards, and WuXi Biologics internal policies and guidelines. * Completing all required training (i.e. safety, equipment etc.). * Contributing to the overall operations and to the achievement of departmental goals. * May be required to assist in other departments or assigned other duties. * Qualifications * BS, MS, or PhD in Life Sciences or related field, with 0 - 2 years of experience in a biopharmaceutical or biological contract testing/manufacturing organization, or a research laboratory. * Hands-on experience in cell culture process/medium development using bench scale bioreactors is preferred. * Strong oral & written communication skills are required. * Ability to work effectively as part of a team and to exhibit effective interpersonal skills. * Ability to take on multiple tasks simultaneously. * Ability to lift 40 lbs * Proficient in Microsoft (Excel, Word, Outlook). Pay range for this position is 20-30 an hour The job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertis and company business needs. .

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 Cape Cod, Chunky, Goldfish, Kettle Brand, Lance, Late July, Pacific Foods, Pepperidge Farm, Prego, Pace, Rao's Homemade, Snack Factory, Snyder's of Hanover. Swanson, and V8. 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… Imagine...working for a company that knows that its people are the key to its success in the marketplace. A company in which achieving extraordinary results and having a stimulating work experience are part of the same process. We cultivate and embrace a diverse employee population. We recognize that people with diverse backgrounds, experiences and perspectives fuel our growth and enrich our global culture. We are looking for an individual who enjoys working in a fast-paced, team-oriented environment, likes to be challenged, and values the opportunity to make a difference. The Associate Scientist R&D will be responsible for supporting the Research & Development activities on the RTS Soup & Innovation Product Development Team. In this role you will be executing projects across the Soup & Broth portfolio, including ready to serve soup and innovation. The scope of the job encompasses the entire Product Development process from idea conception through plant commercialization. What you will do… * Execute work plans for the Ready to Serve Soup Business supporting one or more projects of low to moderate complexity and technical risk. * Demonstrate organizational and planning skills. * Assist with the development and execution of project timelines, which include contingency planning. * Leverage vendor capabilities to expand formulation possibilities and ingredient solves to increase speed to market. * With guidance, develop prototypes to support concept and ideation exploration work and continue to refine the prototypes based on consumer feedback. * Work on the bench and pilot plant line to understand initial feasibility of new products and conduct ingredient screenings during benchtop evaluation. * Conduct trials in the Pilot Plant and/or manufacturing facilities to assess manufacturing capability and consumer acceptability. * Incorporate nutritional and cost parameters into product design. * Demonstrate flexibility and agility by being able to adapt quickly to changes in direction. * Partner with team members to advance projects and be able to function effectively in a cross-functional team environment. Lead cross-functional tastings with business partners and stakeholders. * Communicate plans, results and project risks to vendors, senior functional staff and/or business teams as required. * Work independently to create new concepts based on research, benchmark and creativity solutions. Who you will work with… In this role you will report to the Manager of Research and Development - Soup & Broth. What you bring to the table… (Must Haves) * Bachelor of Science or higher in Food Science or related field. * Minimum of 6 months in CPG or Foodservice industry or related experience with basic or Co-Op food product development experience. It would be nice if you have… (Preferred Skills) * Demonstrated skills in commercializing products/processes in the manufacturing environment are desired. * Creative problem-solving skills. * Technical, culinary, and new product curiosity for food. * Ability to work with ambiguity and seek creative solutions. * Inclination to work in a team environment. * Strong planning and organizing skills. * Ability to synthesize data, interpret, and provide recommendations. * Highly capable with lab practices, running & improving test methods, material preparation, and batch assessment. * Strong planning and organizational skills. * Good written and oral communication skills. * Basic understanding of consumer testing methodologies. * Computer skills include basic fluency in Microsoft Office, and database management. Working Conditions: * Anticipated travel of up to 30% to locations 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 or 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 $57,800-$83,100 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.

Job DescriptionSalary: Princeton NuEnergy (PNE) is excited to announce future opportunities to join our innovative Research & Development team, focused on pioneering advancements in the direct recycling and upcycling of spent Lithium-ion battery materials. Our mission is to deliver a cost-efficient, environmentally friendly solution to the current industry pain points of high operational costs and low efficiency in battery recycling. We aim to solve these challenges by improving battery recycling efficiency and purity, thereby revolutionizing the lithium-ion battery recycling landscape. About Us: PNE is a lithium-ion battery direct recycling and critical materials recovery innovator, founded out of Princeton University. At its core, PNE's patented recycling technology is based on a low-temperature plasma-assisted separation process (LPAS) that does not damage but, rather, reclaims and repairs cathode material from spent lithium-ion batteries and manufacturing scrap at half the cost with significantly lower waste when compared with existing traditional recycling processes. Our state-of-the-art laboratory is located in Princeton, New Jersey, where we are dedicated to pushing the boundaries of sustainable energy technologies. We are building a team of passionate and talented individuals to drive forward our cutting-edge research initiatives. Potential Roles: We anticipate openings for the following positions in the near future: Research Scientist Process Engineer Technician Ideal Candidates: We welcome applications from candidates with expertise in: Battery cathode material synthesis and related research experience. Plasma physics, particularly in device development and experimental applications. Chemical Engineering (with a focus on inorganic chemistry), Materials Science & Engineering, Chemistry, or related areas of study. If you are passionate about sustainability, innovation, and advancing the future of energy storage, we would love to hear from you! Princeton NuEnergy, Inc. is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, gender, sexual orientation, gender identity or expression, religion, national origin, marital status, age, disability, veteran status, genetic information, or any other protected status under federal, state, and local laws.

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

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Biotherapeutics R&D Job Category: Scientific/Technology All Job Posting Locations: Spring House, Pennsylvania, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at *******************/innovative-medicine Johnson & Johnson Innovative Medicine R&D is recruiting for a Scientist, Biologics located in Spring House, PA. We are seeking a Scientist, Biologics to join our innovative team within Discovery, Product Development and Supply (DPDS). Principal Responsibilities: Design and execute experiments to assess high-concentration properties of lead molecules, including viscosity, concentratability, stability, aggregation, and self-association. Set up and manage stability studies; prepare samples for biophysical analysis. Conduct high-throughput biophysical measurements using techniques such as, NanoDSF, GXII, Chromatography (Size Exclusion (SEC), Hydrophobic Interaction (HIC), CIC), Capillary Isoelectric Focusing (cIEF), Dynamic Light Scattering (DLS), Mass photometry. Execute methods of automation workflows: execute methods on Liquid Handlers for sample preparation (mixing, dilution, plate transfer, plate mapping). Independently interpret and communicate experimental results to program teams and senior management. Innovate and implement new techniques to assess developability and biophysical characteristics of therapeutic candidates. Optimize biophysics characterization workflows to improve throughput and data quality. Serve as a Biophysics representative on multidisciplinary project teams, contributing scientific insights and strategic direction. Qualifications: A minimum of a Bachelor's degree in Biochemistry, Protein Analytical Chemistry, Biophysics, Chemistry, or a related discipline is required. Master degree in Biochemistry, Protein Analytical Chemistry, Biophysics, Chemistry, or a related discipline is preferred. A minimum of 5 years of relevant industry experience with a Bachelor's degree or a minimum of 3 years of relevant industry experience with a Master's degree is required. Solid understanding of protein science and biophysical principles is required. Hands-on experience characterizing therapeutic proteins and antibodies using a broad array of biophysical and stability techniques, including SEC, DSF, HIC, GXII, and/or DLS is required. Experience with high-throughput liquid handling systems is preferred. Experience in maintaining written records of work in the form of laboratory notebooks (paper or electronic) is required. Must have excellent verbal and written communication skills. Must have strong interpersonal skills. The ability to report data and present findings to management is required. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (********************************) or contact AskGS to be directed to your accommodation resource. Required Skills: Preferred Skills: Analytical Reasoning, Biochemistry, Chemistry, Manufacturing, and Control (CMC), Coaching, Collaborating, Conducting Experiments, Data Quality, Drug Discovery Development, Molecular Diagnostics, Patent Applications, Pharmacogenetics, Report Writing, Research Documents, Scientific Research, Technologically Savvy, Written Expression

Formulation Scientist Kelly OCG has an opportunity for a Formulation Scientist for our client a leading medical device company in Raritan, NJ. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. This role is a full-time, fully benefited position. As a Kelly OCG employee, you will be eligible for Medical, Dental, 401K and paid time off, including holiday, vacation and sick/personal time. Length of assignment one year Must provide your own laptop Day shift Hybrid - 3 days on site Pay $50-55 an hour depending on experience Responsibilities:Leads formulation design efforts from concept through to prototyping phases, Design Reviews and Validation Collaborate with external suppliers and internal partners to develop products Drive product characterization to ensure rigorous technical understanding and relationships to pre-clinical/clinical outcomes Lead raw material suppliers through raw material iterations, correlating to product design window Drive execution of Learning Plans Participate in multi-functional discussions and design reviews, including product creation at multiple scales (modeling, lab, pilot and manufacturing) Participate in clinical procedures and activities, translating learning into viable prototypes Proven problem-solving skills using analytical technologies is preferred\ Experience with respect to PMA preferred Proven problem-solving skills using analytical technologies is preferred Experience Design of Experiments (DOE) is preferred. Experience in developing protocols and writing completion reports is preferred. Experience developing combination (drug/device) medical devices products is preferred Working knowledge of basic statistics is required. Experience in vitro and ex vivo methods for characterizing prototypes and products is preferred Experience in developing and validating biochemical test methods for finished products and raw materials is preferred Excellent communication, collaboration and influencing skills Demonstrated ability to deliver project outcomes in an ambiguous environment Requires experience managing self-directed work teams Travel up to 20% may be required (domestic and international) QualificationsEducation: Minimum Bachelor's degree required; advanced degree (Ph D) in Chemistry, Chemical Engineering, Pharmaceutical Sciences, Polymer Science, Polymer Engineering, strongly preferred Experience in medical device development is required 5 -10 years ideally Successful experiences in launching new products & formulations to market is required. Experience in biomaterials and material development highly preferred P#1

Our large pharmaceutical client is seeking a Scientist for Protein Biophysical Analysis to join the growing Binding Group. This team focuses on developing and applying preclinical assays to support the discovery of therapeutic candidates. The ideal candidate will have strong expertise in biophysical and biochemical characterization, with a focus on affinity analysis methods. Key Responsibilities Conduct kinetics and affinity analysis of antigens and antibodies using SPR (Biacore, Proteon), BLI (Octet), and KinExA. Perform HPLC analyses to assess hydrophobicity, size, and purity of proteins. Characterize molecules using mass spectrometry (MS). Analyze data, document results, and maintain records in ELNs and LIMS. Maintain lab instruments, including cleaning spray sources, weekly calibration, and preparing calibration solutions. Support assay development, validation, and bioanalysis efforts as needed. Assist in drafting and executing peer-reviewed posters, manuscripts, technical reports, and patent filings. Required Skills & Experience Bachelor's degree in a related field (advanced degree preferred). Hands-on experience with biophysical binding analysis methods, such as: Biacore, LSA, SPR methods (Proteon), BLI (Octet), KinExA Fluorescence anisotropy, RIA, or flow cytometry for affinity determination Solid understanding of protein biochemistry, binding affinity, thermodynamics, and antibody structure. Pharmaceutical experience with mass spectrometry characterization of antibodies (preferred).