Research associate jobs in Franklin, NJ - 436 jobs

United Chemical Technology (UCT) was founded in 1986 by one of the pioneers of Solid Phase Extraction (SPE), Michael Telepchak, who is still active in the Company and continues to works with our team of talented chemist in our research and development department. UCT is a major competitor in the field of silica based phase extraction technology and silane manufacturing. UCT's mission is to establish and maintain a leadership position in the specialty chemical market for organosilicon products. Our products serve the environmental, forensics, food and beverage, clinical, pharma and cannabis industries. As a company, we consistently strive to distinguish ourselves from competitors in terms of service, pricing and quality. To accomplish this goal, we continue to invest in the best people, providing them with the finest tools available. Through excellence, UCT is committed to meeting not only the customer's needs of today but also those of tomorrow. This role involves developing applications and opportunities in our sample preparation product lines through authoring articles, white papers, posters, and technical presentations. The candidate will be a valued core member of the UCT R&D team, assisting with customer technical support, providing on-site support when required, and traveling with the sales team as needed. Key duties and responsibilities include: Drive R&D initiatives by executing laboratory project goals under the guidance of the R&D Team Manager, contributing to new product development, experimental evaluations, and preparation of application notes. Independently initiate and develop SPE applications by exploring innovative uses for existing products to expand their applicability in forensic and toxicological workflows. Staying current with emerging trends and techniques and applying UCT products to new applications for evaluation and comparison. Collaborate with Quality Control as needed to design evaluations and experiments that enhance product testing and performance. Publish at least two scientific papers or posters annually on newly developed applications of UCT products. Actively participate in professional organizations (e.g., AAFS, SOFT) to expand knowledge of SPE applications in forensic and toxicological fields. Provide timely and accurate technical support for customer inquiries and sales requests, addressing their needs effectively. Support our technical continuing education program by developing and maintaining training and workshops for the Sales Team, distributors, and customers, educating them on the effective use of UCT products and relevant forensic toxicology knowledge to enable productive sales interactions and technical discussions. Must be available to travel up to 30% of time to include applicable conferences and tradeshows, domestic/international customer visits, and distributor training. Promote a culture of safety, collaboration, and effective teamwork across the group and other company departments. Other duties as assigned. Skills & Abilities: Strong experience in sample preparation method development in an R&D environment, particularly with SPE and QuEChERs products (preferred) Proven ability to work independently in the laboratory, utilizing LC-MS/MS and GC-MS instrumentation, while applying analytical problem-solving skills. Ability to evaluate current products and recommend improvements for UCT's products and their applications. Highly adaptable and organized, capable of managing multiple projects simultaneously and delivering results on schedule. Effective collaborator and team leader, with strong communication skills to convey complex technical information and support cross-functional decision-making. Education & Experience: Bachelor's degree in Forensic Toxicology, Chemistry, or a related field, with an emphasis on chemical analysis; Master's degree preferred. Minimum of 3 years' experience in a forensic laboratory performing drug analysis and method development. Hands-on experience using sample preparation products (SPE, QuEChERS) in conjunction with GC, LC, GC-MS/MS and LC-MS/MS. Demonstrated ability to develop new methods, establish validation criteria, and define specifications. Familiarity with competitors' products and a strong interest in toxicological analysis. Awareness of current industry trends and emerging approaches in analytical method development. UCT is committed to the principles of equality in employment. It is contrary to our policy to discriminate against individuals because of race, color, creed, ethnicity, religion, ancestry, age, national origin, sex (including childbirth, or related medical conditions), sexual orientation, gender identity or expression, genetic information, physical or mental disability, union affiliation, citizenship status, marital status, pregnancy, military or veteran status or any other status prohibited by applicable federal, state or local law (“protected category”). Equal employment opportunity applies to all terms and conditions of employment, including hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation, and training. UCT explicitly prohibits any form of unlawful employee harassment or discrimination based on any of the characteristics mentioned above. Improper interference with the ability of other employees to perform their expected job duties will not be tolerated.

Immediate need for a talented Scientist 2, Research & Development. This is a 10 months contract opportunity with long-term potential and is located in Skillman, NJ (Hybrid). Please review the job description below and contact me ASAP if you are interested. Job ID: 26-00524 Pay Range: $35 - $43/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Hours: 8:30am to 5:00pm (Monday through Friday). 86 Morris Avenue Summit, NJ 1 day per week. May fluctuate based on needs. A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline. Key Requirements and Technology Experience: Key skills; Consumer Products - Skin Health BA Degree 2 to 4 years' experience Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

Are you an experienced Scientist - Cell-Based Assays with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Scientist - Cell-Based Assays to work at their company in Rahway, NJ. Position Summary: We're seeking a hands-on scientist to execute high-throughput cell-based assays in 384-well format. You will culture and plate cells, dispense compounds using the Echo, run diverse detection readouts, and analyze dose-response data to deliver high-quality EC50 results for discovery programs. Primary Responsibilities/Accountabilities: Maintain, expand, and plate mammalian cell lines for 384-well assays Set up and execute assays with compound dispensing via Labcyte/Beckman Echo Run and optimize detection formats (e.g., luminescence, cAMP, HTRF/TR-FRET, fluorescence) Generate dose-response curves (4-parameter logistic fits) and report EC50/IC50 with QC Troubleshoot assay performance, optimize Z' factors, and document SOPs/results Collaborate with discovery teams to prioritize studies and timelines Additional responsibilities may include setting up Western blot assays and learning how to run in-cell westerns Qualifications: BS/MS/PHD in Biology, Pharmacology, Biochemistry, or related field; BS with 5+ years, Masters with 3+ years and PHD with 1+ year of industry or equivalent lab experience. Proficiency in mammalian cell culture and 384-well assay workflows Experience with plate readers and assay platforms (e.g., cAMP, HTRF, luminescent assays) Strong data analysis skills: 4PL curve fitting, EC50/IC50 determination, and curve QC (e.g., R^2, top/bottom constraints) Detail-oriented, organized, and comfortable in a fast-paced, high-throughput environment Preferred: Experience with automation/LIQ handlers, LIMS/ELN, and statistical QC (Z', CV, S/B) Familiarity with GraphPad Prism, ActivityBase, or equivalent analysis tools Hands-on experience with Echo acoustic dispensing.

From the very beginning, we have been focusing on the science. We came together as a team of experts, committed to quality, driven by excellence, and dedicated to experimentation. Though we faced many challenges, we remained fearless in our research and rigorous in our thinking, pushing ourselves to work harder. However, what affected us the most was the enormous burden patient's bear and the difficulties they face, which drove us to think about what's next. We believe it is time to accelerate and expand that transformation. At Legend Biotech, we are excited to bring clinical trials to patients in our pursuit of a cure. While we are focusing on CAR-T in multiple myeloma, we firmly believe the prospects of cellular therapy stretch beyond just one disease or indication. The spark of hope is lit. At Legend Biotech, we are using that hope to ignite the future of CAR-T cell therapy. Job Description Role Overview: Legend Biotech is a clinical stage biopharmaceutical company focused on the discovery and development of novel cell therapies for oncology, immunology and infectious disease indications. We are currently seeking a talented and motivated candidate to join the R&D cell biology and immunology lab at US site. The successful candidate will contribute to the company's efforts to develop next-generation cell therapies in solid tumor malignancies. The successful candidate will have cell biology and immunology background, and expect to work in a collaborative cross-functional team environment, perform experiments, organize and analyze results, communicate effectively to support R & D teams. Major Responsibilities: Prepare cell banks of all the cell lines for R&D department usages Maintain biological reagents inventory stocks for R&D research. Maintain all laboratory instrument records. Comply with the correct procedures, policies, and health and safety regulations. Conduct laboratory tests, analyze results, and document your findings. Stay informed with the latest industry trends, techniques, and best practices. Document all activities, results and report to management as needed. Classify and label samples. Must also work well as a member of a collaborative team, be highly organized, have attention to detail and excellent time-management skills. Other duties assigned Qualifications Education: B.S. in bioscience field or cell biology and immunology Experience: · 0-2 year with B.S. Industry/academic experience in Cell Biology Key Capabilities, Knowledge, and Skills: Prior experience with cell culture and sterile technique Knowledge of cell biology and immunology Knowledge of lab procedures and understand the importance of maintaining a clean workspace by following all lab regulations for health and safety Flexibility to work on another lab support tasks Additional Information Legend Biotech USA Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech USA Inc. maintains a drug-free workplace.

Job Title - Research Associate Co-op, Analytical Sciences Work Location - Cranbury NJ WuXi Biologics is a is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing. WuXi Biologics' achievements are a direct result of the efforts made by our employees. We have built an extraordinary team motivated by our PROUD culture of Passion, Reward, Opportunity, Unity, and Determination. WuXi Biologics offers exciting job opportunities and careers around the globe. We currently employ over 12,000 people and provide services to more than 600 customers worldwide, including all the top 20 biopharmaceutical companies Job Summary We are looking for an enthusiastic co-op to join our Analytical Sciences team. This is a great opportunity for students interested in pharmaceutical or biotech R&D to gain practical lab experience and build a solid foundation in analytical method development and testing. Responsibilities * Assist in the execution of analytical tests, including but not limited to HPLC, CE, UV, and mass spectrometry. * Assist with sample preparation, buffer preparation, and instrument operation. * Perform data processing and documentation in compliance with laboratory standards. * Maintain accurate lab records and assist in generating technical reports. * Participate in equipment calibration, maintenance, and inventory management. * Work closely with scientists on assigned research or development tasks. Qualifications * Bachelor's or Master's student in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field. * Basic knowledge of chromatography, electrophoresis, and other analytical techniques. * Hands-on experience on lab work. * Experience with Empower or other data acquisition software. * Understanding of biologics development and regulatory expectations. * Basic knowledge of chromatography, electrophoresis, and other analytical techniques. * Strong organizational skills and attention to detail. * Effective communication and teamwork abilities. * Willingness to learn and good time management. * Proficient in Microsoft Office (Word, Excel, PowerPoint). The pay range for this position is $20-$30hr (based on education level) 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 expertise and company business needs. 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, or protected veteran status and will not be discriminated against on the basis of disability

We are seeking a scientist to fill an open position in the PBMC production group within biomarker technologies. The primary focus of this team will be processing high quality PBMC samples from whole blood of patients on various clinical trials for downstream flow cytometry analysis. The focus of this position is only on the production of PBMCs from whole blood. The scientist will also participate in the oversight of QC for PBMC samples at external vendors and evaluation of new PBMC technology and techniques as available. Experience with multiple PBMC processing and storage techniques is a plus. Qualifications PBMC -peripheral blood mononuclear cell Additional Information Please feel free to call me @ ************ to discuss about this job.

Clinical Research Investigator (MD/DO) DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 in the country, is looking for an Investigator for our site in Jersey City, NJ. This individual will conduct all clinical trials (studies) according to ICH, GCP, local regulations, study protocols, and company processes. Responsibilities Ensures the medical well-being and safety of the participants through the safe performance and execution of the studies. Assists in maintaining clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site. Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety, and retention of participants. Interprets protocols and IB and participates in initiatives to strategize for patient recruitment. Carries out clinical evaluation and assessment of participants to ensure eligibility to enroll in studies. Ensures and protects the welfare and safety of participants through ethical conduct. Fulfills and complies with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations. Exercises meticulous attention to detail in documentation and patient care. Requirements Medical license (MD, DO) - New Jersey 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator) Bilingual Spanish a plus Flexible hours - schedule can be tailored as required.

Job Title: Contractor at Research Associate Scientist level Division/Functional Area: Research & Development TMS, Development Biological Sciences R&D, is seeking a highly motivated junior scientist to support a development project in the Regenerative Medicine area. This contractor position offers an excellent opportunity for individuals seeking valuable industry experience and growth in a dynamic environment. The successful candidate will perform laboratory experiments to evaluate and **characterize biologic** and **synthetic implantable materials** . Knowledge and familiarity with biomaterial characterization techniques (DSC, SEM, etc.), biochemical analytical testing (such as colorimetric assays), digital image analysis, and mechanical testing methods (e.g. Instron testing) is preferred. Prior experience in **ECM biology, tissue engineering & regeneration** , or **biomaterials** is highly desirable. We are looking for someone who is naturally inquisitive, detail oriented, learns quickly, and thrives in a fast-moving research setting. The candidate will be expected to organize, analyze, and interpret experimental results with substantial independence, while receiving guidance from senior personnel and collaborating extensively with other Scientists and Research Associates. **Top 3-5 skills, experience or education required** 1. BS in material science, biomedical engineering or related field 2. 1+ years of hands-on laboratory experience (academic lab experience for fresh graduates or industry experience are both okay) 3. Knowledge and familiarity with one or more of the following instruments: DSC, SEM, Instron 4. Quick learner **Key Responsibilities** - Independently conduct laboratory experiments to generate reliable and consistent data in a timely manner. - Document, discuss, and modify experimental studies as needed in collaboration with other team members and/or project lead. - Summarize data and assist project lead in maintaining project documentation. **Qualifications** - Bachelor's degree in material science, biomedical engineering or a related field with 1+ years of academic or industry laboratory experience - Experience with performing and troubleshooting a wide variety of **material characterization** assays is desired - Demonstrated ability to quickly learn new concepts, skills and techniques - Capable of contributing independently but also work successfully in a highly collaborative scientific environment - Possess strong written and oral communication skills - Working knowledge of MS Office (Excel, Word, PowerPoint) and basic understanding of statistical analyses is a plus - Meticulous attention to detail and diligence in record keeping **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.

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 Include tracking of activities provided by external contract laboratoreis both clinical and pre clinical. Ensures all necessary documentation is inmplace (ie statements of work/assay development requirements etc). Additional responsibilities include reviewing/distributing all external research reports. Additional Information Regards, Anuj Mehta ************

Biologist needs BS requires 3-5 years and MS requires 1 -3 years of previous related experience. Biologist needs requires: BS requires 3-5 years and MS requires 1 -3 years of previous related experience. Good working knowledge of cGMP regulations is required. Ability to work independently with moderate supervisory guidance. Excellent teamwork and communication skills. Attentive to detail. Good computer skills BS or MS in a related science such as a Biology or Biochemistry is required Biologist duties: Monitor laboratory equipment for temperature and conformance to specifications. Apply acceptable cGMP practices during execution of all work tasks Work independently with minimal supervisory guidance. Exhibit strong teamwork skills. Use scientific expertise to provide assistance for troubleshooting, laboratory investigations and problem resolution. Suggest process improvements to QC management

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.

The Research Assistant I will be responsible for assisting the clinical research staff in conducting clinical research trials. DUTIES & RESPONSIBILITIES Completing DMCR-required training, including GCP and IATA. Maintaining a working knowledge of current FDA regulations, GCP/ICH guidelines, organizational SOPs, guidance documents, and study protocols. Assisting in the collection and recording of patient data per Sponsor requirements via the respective EDC system. Timely and accurately assist in collection, management, and shipment of subjects' samples, and/or specimens Completing Sponsor-required training prior to study-start, including, but not limited to Sponsor-provided and IRB-approved protocol All amendments Investigator Brochure Sponsor-specified EDC and/or IVRS This includes completing the above-mentioned training prior to any study-related procedures being conducted on that said protocol should the RA be added to a protocol post-study start. Maintaining clear, concise, accurate, and legible records. Being prepared for and available at all required company meetings and monitoring visits for their assigned protocols at their respective site(s). Utilizing the most recent version of the Protocol, Informed Consent, and Investigator Brochures at their respective site(s). Assisting in the compilation and organization of all regulatory and administrative binders for their assigned protocols at their respective site(s) upon initial receipt of and wherever applicable. Assisting in the creation of source documents for their assigned protocols at their respective site(s). Conducting patient visits. Assisting in reporting Adverse and Serious Adverse Events to the appropriate authorities per Sponsor. Assisting in addressing and resolving issues from internal/external audits and monitoring letters for all assigned protocols at their respective site(s) in a timely manner. Assists with all other aspects of the study and conducts as needed. Any other matters as assigned by management. KNOWLEDGE & EXPERIENCE Education: High school diploma or equivalent required Experience: Prior experience in clinical research is not required but preferred Credentials: Phlebotomist certificate preferred Medical Assistant Certification preferred Knowledge & Skills: Knowledge of medical terminology required Must be detail-oriented and demonstrate attention to detail Excellent customer service skills Excellent computer skills

We are seeking a motivated In vivo Lab Technician to support preclinical and translational research studies. This role involves hands-on animal care and technical support for in vivo pharmacology, toxicology, and disease models. Candidates with ALAT certification are preferred. The incumbent works cross-functionally with internal departments and external resources on preclinical and translational research related issues. The In vivo Lab Technician supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. Perform daily animal husbandry, health checks, and cage maintenance. Assist with in vivo study execution including dosing (IV, IP, SC, PO), animal monitoring, and data collection. Support blood, tissue, and organ sample collection under supervision. Maintain accurate animal records and study documentation. Ensure compliance with IACUC protocols, AAALAC standards, and animal welfare regulations. Assist with vivarium maintenance and sanitation procedures. Work closely with scientists and veterinary staff to support study timelines. Perform other tasks and assignments as needed and specified by management. Qualifications Required Knowledge, Skills and Abilities: Ability to follow SOPs and regulatory requirements. Proficiency with Microsoft Office Ability to work independently and collaboratively, as required, in a team environment consisting of internal and external team members. Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects Education and Experience Requirements: Required: Associate's or Bachelor's degree in Biology, Animal Science, or related field (or equivalent experience). Hands-on experience working with laboratory animals (rodents preferred). Strong attention to detail and record-keeping skills. Preferred: Experience with rodent handling, restraint, and basic procedures. Familiarity with dosing techniques (IV, IP, SC, PO). Experience in a preclinical CRO, biotech, or pharmaceutical environment. Understanding of IACUC, AAALAC, and animal welfare regulations. Physical Demands: N/A Working Conditions: Laboratory and office environment Certificates and Licenses required: ALAT certification (AALAS) preferred Compensation: $55,000 to 75,000 per annum NJ Bio, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to their race, color, sex, religion, age, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability or any other characteristic protected by applicable federal, state, or local laws.

About Us: Shamrock Technologies is a family-owned business which prides itself on its enterprising spirit. This atmosphere inspires associates to pursue their ambitions without the boundaries of classic organizational structure. Headquartered in Newark, New Jersey, Shamrock Technologies is one of the world's largest processors of micronized polytetrafluoroethylene (PTFE), as well as a leading worldwide manufacturer and supplier of a broad line of specialty products. Our materials are found in Inks and Coatings, Lubricants, Grease, Thermoplastics, and more. Using advanced technology and sophisticated production equipment, combined with our state-of-the-art Application and R&D laboratory facilities, Shamrock creates products to help customers meet their challenging formulation needs. Shamrock differentiates itself by hiring associates with an approach to thinking that actively seeks change rather than waiting to adapt to it. Our business embraces originality, curiosity, critical questioning, service, and continuous improvement, while creating a work culture that values cooperation. Summary: We are seeking a hands-on, innovative Research Chemist to support product development and applications research within the Wax Additives business. This role focuses on designing and conducting laboratory experiments, characterizing materials, and generating data that help bring new wax powders, dispersions, emulsions, and surface-modified products to market. The Research Chemist will work closely with the Technical Director and cross-functional teams to translate customer needs into technical solutions. Primary Responsibilities Plan, execute, and document lab experiments to develop new wax additives and improve existing products. Formulate and test emulsions, dispersions, blends, and surface-modified waxes for coatings, inks, and plastic applications. Operate and maintain laboratory equipment such as mills, mixers, particle size analyzers, DSC, FTIR, and rheometers. Collect, interpret, and summarize experimental data to guide decision-making. Prepare technical reports and communicate findings to the technical teams. Screen new raw materials and evaluate competitive technologies. Support scale-up trials by providing lab-to-pilot correlations and data. Assist in preparing technical presentations and samples for customer trials. Follow established safety protocols and maintain a clean, organized lab environment. Ensure accurate documentation and compliance with internal and external standards. Qualifications Education and Experience Bachelor's degree in Chemistry, Polymer Science, Materials Science, or Chemical Engineering. 0-5 years of experience in a chemical, polymer, or coatings laboratory (industrial or academic research). Hands-on experience with emulsions, dispersions, or polymer/wax formulations is highly preferred. Experience with polyamide chemistry or related polymer modification techniques is a plus. Professional Skills Strong experimental design and data analysis skills. Proficiency with common lab instrumentation (particle size, DSC, FTIR, rheology). Creative problem-solver with curiosity and initiative. Effective communicator with ability to work cross-functionally. Comfortable with multitasking in a fast-paced environment. Work Environment & Physical Requirements: Laboratory-based position with occasional pilot plant and production floor exposure. Required to wear PPE and complete safety training. Able to stand/sit for extended periods of time, may include bending/stooping. Prepared for prolonged periods sitting at a desk and working on a computer. Compensation package We offer a competitive salary complemented by an annual performance-based bonus. Our comprehensive benefits package includes generous paid time off hours, a 401(k) plan with employer matching, comprehensive healthcare coverage, employer-sponsored life insurance, and additional benefits designed to support your well-being and financial security. Equal Opportunity Statement Shamrock Technologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, 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. Request for Assistance If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting Human Resources via email at ***************************. Reasonable Accommodation Applicants with disabilities may contact Shamrock Technologies via telephone, e-mail, and other means to request and arrange accommodation. If you need assistance to accommodate the disability, you may request accommodation at any time. Please contact the Shamrock Technologies Human Resources department at ***************************.

The Scientist-2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment. Essential Functions: * Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. * Develops and optimizes new and existing analytical methods for qualification and release testing of products. Develops stability indicating methods and performs methods validation. * Provides timely responses to all internal and external inquiries. * Ensures deadlines are met for product development schedules, and checks that technical and compliance requirements are met. * Evaluates, recommends, and implements new analytical technologies and instrumentation for testing. * Assists with training other members of the analytical development team. Additional Responsibilities: * Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance.

Collectors is the leading creator of innovative technology that provides value-added services for collectors worldwide. We grade, authenticate, vault, and sell millions of record-setting collectibles, all while modernizing and digitalizing the process to further our mission of helping collectors pursue their passions. We're always on the lookout for talented people to join our growing team. Our services span collectible coins, trading cards, Funko Pops!, video games, event tickets, autographs, and memorabilia. Our subsidiaries include PSA, PCGS, SGC, and Card Ladder. Since our founding in 1986, we have graded and authenticated millions of items. We employ more than 1,900 people across our headquarters in Santa Ana and offices in Jersey City, Tokyo, Shanghai, Hong Kong, Toronto, Guadalajara, Dallas, and Paris. PSA is looking to add a Research Specialist to their team! Our Research Specialists physically review, identify, and classify sports and non-sports cards, tickets, packs, pins and coins for entry into the PSA specification database. What You'll Do: Identify sports cards and associated varieties (baseball, football, and all other major sports card releases) Identify non-sports cards (vintage cards such as R145 Gum, Inc. Superman to Wacky Packs to modern releases like Pokémon and Yu-gi-oh) Identify event tickets (sporting events, concerts) Research by means of trade magazines, books and internet Communicate effectively with other divisions Communicate with manufacturers such as Topps, Upper Deck & Panini Maintains and updates database Who You Are: Firsthand knowledge of trading cards, tickets and other sports collectibles Strong research and cataloging skills Strong written and verbal communication skills Effective problem-solving skills Physical Requirements: Computer Use: Typing, mouse work, and sitting and looking at a computer potentially for long periods of time. Hand Use: Regular hand use for various tasks. Hearing Requirements: Ability to hear alarms, signals, and verbal instructions. Lifting and Carrying: Ability to lift, carry, and move materials up to 25 pounds. Sitting or Standing: Ability to sit or stand for extended periods of time. Hourly Rate: The reasonable estimated hourly rate for this position is $17. Actual compensation varies based on a variety of non-discriminatory factors, including location, job level, prior experience and skill set. Collectors uses e-Verify to validate your ability to work legally in the United States. We are aware that there are instances where individuals are receiving job offers that fraudulently allege to be from Collectors or one of our business units. This type of fraud can be carried out through false websites, through fake e-mails claiming to be from the company or through social media. We never ask for personal information such as your bank account, Social Security numbers or National IDs, nor do we send or request payments for the purchase of business-related equipment. If you suspect fraud, please reach out to *******************. We are committed to equal employment opportunity regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, veteran status, or other class protected by applicable law. We believe that a team that represents a variety of backgrounds, perspectives, and skills will better service the diverse community of collectors we support. If you require an accommodation to apply or interview with us due to a disability or special need, please email ********************* . U.S. residents: for disclosures relating to personal information we collect during the employment application and recruitment process, please see our Privacy Notice for U.S. Applicants . If you are based in California, you can read information for California residents here .

The R&D Associate will support the Product Development team by managing tastings, coordinating projects, producing samples, and maintaining the R&D kitchen. This role requires strong organizational skills, attention to detail, and a good understanding of food production processes. Experience in R&D or food production is preferred. Key Responsibilities: Tasting Preparation: Organize tastings, ensure proper labeling, and handle product storage. Project Coordination: Set up and document product development kickoff meetings. Sample Production: Manage sample runs, gather data, and coordinate with QC and production teams. Kitchen Management: Maintain cleanliness, organize supplies, and operate R&D kitchen equipment. Product Knowledge: Understand coated products and production processes. Documentation: Track all production and sample data, ensuring accurate records. Qualifications: Experience in R&D or food production (preferred). Strong organizational and time management skills. Familiarity with food safety practices. Bilingual proficiency in English and Spanish (preferred). Physical Requirements: Ability to lift equipment and stand for long periods during kitchen tasks. Location: Newark, NJ 07114 (In-person, relocation required) Job Type: Full-time Pay: From $50,000 per year Schedule: Monday to Friday Benefits: 401(k), health insurance

Job Description We are on the prowl for a Lab Technician to join our Mount Olive, New Jersey team at Symbiotic Research, a Tentamus North America company! If you are deeply passionate about science and enthusiastic about broadening your expertise, we invite you to apply today and become a vital part of our mission. How you will contribute as a vital part of our team: The Laboratory Technician will contribute to a world class laboratory by performing various laboratory duties under the direction of scientific staff which may include: Performing sample extraction, workup and pipetting. Adhere to all laboratory safety practices and follow applicable GLP regulations and government guidelines to conduct studies. Document all work performed following GDP principles. Communicate clearly with laboratory staff and scientists. Rely on SOPs and/or methods to perform the functions of the job. Prepare routine solutions; upkeep with laboratory cleanliness, organize all lab supplies to be easily accessible for all and provide laboratory maintenance. Maintain and calibrate the laboratory instruments as assigned. Support laboratory staff as needed. Position & Schedule Full-Time, 40 hours per week, Monday - Friday 8:30AM - 5:00PM or 9:00AM - 5:30PM with a 30-minute lunch break. Qualifications Our ideal candidate will be authorized to work in the United States indefinitely without restriction or sponsorship; have a BS in Biology preferred or related science field or experience working in a scientific laboratory setting; and an ability to work both independently and within a team. Other items include: Has knowledge of the use, maintenance, and/or calibration of most GLP equipment. Knowledge of laboratory operations. Must be able to work in a flexible environment, perform a variety of tasks and prioritize work. Ability to work under minimum supervision. Ability to implement scientific procedures and processes involved with residue, environmental fate and metabolism studies. Exhibit excellent oral and strong written communication skills. Self-sufficient in planning and executing daily responsibilities and the ability to tend to experimental details and attention to detail. Good computer skills and being adept with standard software (e.g. Windows, Excel, Word). Must be able to read, understand, and follow SOPs, policies and regulations, and provide general laboratory support. Required to frequently stand, walk, and sit. The employee must occasionally lift and/or move up to 40 pounds. What's in it for you? $16 per hour and a comprehensive and low-cost benefit plans (medical, dental, vision, disability, life insurance, HSA) Ample PTO and a matching 401k About Tentamus: Labs for Life . We are a global network of full-service accredited analytical laboratories providing crucial quality and safety analysis for clients locally, nationally, and beyond using proven methods of chemistry and microbiology. Many of the products you use and consume daily rely on Tentamus labs. With 20 labs in North America and growing (100 globally), we celebrate having talented diverse scientific and service-oriented professionals. Learn More: Tentamus Website | Symbiotic Research Website Job Posted by ApplicantPro

Biologist needs 3 years of experience Biologist requires: Degree in Biology or other sciences Assays Documentation Labs MS Office Vell biology Molecular, cell biology immunology Biologist duties: .Conduct experiments to identify and validate drug targets. Support assay design, optimization, validation, and data analyses. Design and execute molecular and cell biology experiments. Troubleshoot and analyze complex data in support of drug discovery projects. Presents results and conclusions both orally and written.