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Job Description QC Analyst I–III Relocation Package Available (U.S. Citizens Only) Global Life Science Hub is recruiting on behalf of a rapidly growing biopharmaceutical company in New Jersey seeking QC Analysts (Levels I–III) to join their expanding Quality Control team. This is an exciting opportunity to contribute to the development and manufacturing of biologics in a state-of-the-art GMP facility, with a full relocation package offered for qualified U.S. citizens willing to move to New Jersey. Role Overview: As a QC Analyst, you will play a key role in performing analytical and microbiological testing to ensure product quality and compliance with regulatory standards. The role requires a minimum of 1 year of hands-on QC or GMP laboratory experience in the pharmaceutical/biotechnology industry. Key Responsibilities: • Perform analytical and/or microbiological testing of raw materials, in-process samples, and finished products under GMP., • Execute assays such as PCR, ELISA, HPLC, flow cytometry, and cell-based assays (depending on level and background)., • Support method qualification, validation, and transfer activities., • Document and review laboratory results in accordance with ALCOA+ and data integrity standards., • Contribute to deviation investigations, CAPAs, and change controls., • Maintain, calibrate, and operate laboratory instruments to ensure readiness for use., • Participate in audits, inspections, and continuous improvement initiatives. Requirements: • Bachelor’s or Master’s degree in Biology, Biotechnology, Chemistry, or related field., • Minimum of 1 year QC or GMP laboratory experience is required., • Analyst I: 1–2 years QC experience., • Analyst II: 2–4 years QC experience in GMP biopharma., • Analyst III: 4–6+ years QC experience with expertise in analytical/cell-based methods and mentoring., • Strong knowledge of GMP, FDA, and ICH guidelines., • Detail-oriented with strong documentation and organizational skills. Why Apply? • Competitive compensation and benefits package., • Relocation package offered exclusively to U.S. citizens willing to relocate to New Jersey., • Career development opportunities across QC levels with exposure to biologics and cell/gene therapy., • Join a collaborative and growing biopharma company shaping the future of medicine.

Company Description JAI Development is a food and beverage innovation lab specializing in product formulation and production operations management across diverse product categories. JAI Development helps emerging CPG brands reach their goals. JAI Development partners with a network of industry professionals to support these brands. The company has worked on award-winning projects at both local and national levels. Role Description This is a full-time on-site role for an Associate R&D Beverage Formulator located in Brooklyn, NY. The Associate R&D Beverage Formulator will be responsible for assisting with the formulation of new beverage products, conducting research and development activities, and utilizing laboratory skills to test and refine product formulations. Day-to-day tasks include supporting the R&D team with analytical assessments, collecting and analyzing data, and effectively communicating findings and progress within the team. Qualifications • Experience in Research and Development (R&D) and strong Research skills, • Proficient in Laboratory Skills and Analytical Skills, • Excellent Communication skills, • Highly organized with attention to detail, • Bachelor's degree in Food Science, Chemistry, or related field, • Ability to work collaboratively and independently in an on-site setting, • Experience in the food and beverage industry is a plus, • Desire to work in a fast-paced environment, collaborating with a team of professionals., • Detail oriented, striving for perfection but ability to learn from failure.

Job Description Magic Spoon reimagines your childhood breakfasts favorites with more protein, less sugar, and more fun. Since launching in 2019, we've brought our unbelievably tasty cereal to over one million customers online and over 20,000 stores nationwide. With our recently launched Protein Treats and Protein Granola we're continuing to find new ways to make mornings magical - all made possible by our incredible team. We’re looking for a passionate and detail-oriented Food Scientist to help fuel our product innovation and drive best-in-class quality as we expand in both retail and DTC channels. Reporting to our Senior Manager, Product Development, you’ll play a critical role in formulating, optimizing, and commercializing new loops (and maybe even some new breakfast surprises) for our growing customer base. We are open to relocation for this role, so you do not need to based in NY to apply. However, this role requires on-site presence in our NYC office up to 5 days per week, with exact in-office expectations determined by business needs. In this role you’ll: • Manage formulation and product development projects from bench-top concept through to commercialization, working closely with internal and external partners, • Design, plan, and execute lab-based experiments and pilot plant/commercial scale-up trials to optimize product quality, shelf life, and manufacturing efficiency, with support from manager, • Analyze ingredient functionality, processing parameters, and sensory and consumer feedback to iterate and refine product performance, • Evaluate, qualify, and partner with new and existing raw material suppliers in collaboration with procurement and FSQR, ensuring all specifications and compliance standards are met, • Ensure regulatory and nutritional compliance for all product prototypes and final formulas, maintaining internal documentation (Genesis, master BOMs, etc.), • Conduct analytical and sensory testing; document results to ensure products meet Magic Spoon’s high standards for flavor, freshness, and nutrition, • Support and maintain lab inventory levels, following SOPs and healthy restock procedures, • Proactively identify and troubleshoot challenges in ingredient sourcing, production, or quality, proposing innovative solutions, • Collaborate effectively with cross-functional teams, including operations, supply chain, procurement, marketing, and FSQR, to ensure a seamless transition from R&D to launch, • BS or MS in Food Science, Food Chemistry, Nutrition, or a related technical/science discipline, • 2-5 years relevant experience in food product development, formulation, or technical applications, ideally within CPG, ingredient, or startup environments. (Relevant internships or co-op experience welcomed), • Familiarity with product development lifecycle from concept through commercialization, • Hands-on laboratory experience in benchtop prototyping, analytical testing, and/or sensory evaluation, • Strong knowledge of food safety, ingredient functionality, and basic regulatory/Nutrition Labeling requirements (FDA, USDA, etc), • Track record of successful cross-functional collaboration and project documentation/management, • Excellent organizational and communication skills; highly detail-oriented with a strong sense of ownership and urgency, • Enthusiasm for startup energy, creative problem-solving, and a love of breakfast!, • Travel up to 50% (at peak time) for supplier visits, manufacturing trials, co-manufacturer oversight, trade shows, or other business needs, • Must possess a valid driver's license and maintain eligibility for business travel., • This role requires international travel to Canada. Candidates must hold or be able to obtain a valid passport for international travel., • Ability to stand for extended periods while conducting experiments, product trials, or working at lab benches and pilot plant equipment., • Frequent walking within laboratory, production, or R&D facilities., • Occasional lifting, carrying, and moving of materials, equipment, and ingredient containers (typically up to 25–50 pounds)., • Ability to perform work in labs, kitchens, pilot plants, or manufacturing environments that may be:, • Warm or cold (depending on the product being tested)., • Humid or dry., • Exposed to strong odors from flavorings, ingredients, or cleaning agents., • Exposure to food allergens, powders, or dust depending on the nature of product development., • Ability to safely operate and troubleshoot food processing and lab equipment., • Frequent use of hands to handle laboratory tools, small-scale processing equipment, packaging prototypes, or ingredient samples., • Precision required for measuring, weighing, and mixing formulations accurately., • Ability to operate computers, analytical instruments, and specialized lab equipment., • Strong sensory abilities for:, • Visual inspection of products (color, consistency, appearance)., • Taste and olfactory evaluation (flavor development, sensory testing). Benefits • Competitive salary & equity, • Bonus eligibility, • Open to offering relocation stipend for eligible candidates, • 100% covered Health, Vision, Dental insurance, • 401(k), • Generous parental leave, • Flexible vacation, • Catered lunch in office, • Dog friendly office, • Unlimited cereal ✨

Job DescriptionQuality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle. • Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients., • Support routine GMP testing as assigned. Mentor and train team members, • Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements., • Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports., • Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data., • Identify, evaluate, and implement continuous business process improvements., • Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS)., • Provide support during laboratory investigations., • Train QC personnel during method transfer and validation. Provide support during equipment qualification., • Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices., • Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures., • Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing.REQUIREMENT, • B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products., • 8-10 years of experience in the areas of method development, validation, and transfer., • Direct GMP Experience., • Proficiency in project management skills and tools., • Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc., • Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs., • Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required., • Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution., • Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team., • Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction., • Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external., • Must be familiar with GMP lab environment and Aseptic techniques.Working EnvironmentMust have the ability to work in a team-oriented environment and with clientsMust be able to work during the weekend, holidays, or overtime and as required by the companyMay be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluidsMust utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogenMust have the ability to work with specialized equipmentMust be able to handle the standard/moderate noise of the manufacturing facilityMay work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Job Description Job Summary Customer is one of the world’s fastest-growing AI companies accelerating the advancement and deployment of powerful AI systems. They help customers in two ways: Working with the world’s leading AI labs to advance frontier model capabilities in thinking, reasoning, coding, agentic behavior, multimodality, multilinguality, STEM and frontier knowledge; and leveraging that work to build real-world AI systems that solve mission-critical priorities for companies. Role Overview: · In this role, you will be working on projects to help fine-tune large language models (like ChatGPT) using your strong analytical and english comprehension skills. · The ideal candidate should have a solid foundation in Physics/Chemistry/Mathematics or Biology (STEM), particularly at the level expected in college/engineering entrance exams, as well as graduate or PhD-level programs. · You should be able to break down complex STEM concepts into simple, clear explanations and work efficiently. · The projects will also help you learn how to leverage AI to be a better analyst. This is your chance to future-proof your career in an AI-first world! Job Responsibilities What does day-to-day look like: · Design and solve challenging STEM problems to probe the limitations of large language models. · Create clear, high-quality, step-by-step solutions with well-articulated reasoning. · Collaborate with LLM researchers to align problems with evaluation goals, especially in areas where models typically struggle (e.g., abstraction, multi-step reasoning, symbolic manipulation). · Help define new evaluation benchmarks based on STEM curricula spanning early undergraduate to PhD-level topics. Essential Skills Requirements: · Analytical Skills: Good research and analytical skills · Feedback Skills: Ability to provide constructive feedback and detailed annotations. · Creative Thinking: Creative and lateral thinking abilities. · Communication: Excellent structured communication and collaboration skills in a remote setting. · Independence: Self-motivated and able to work independently in a remote setting. · Technical Setup: Desktop/Laptop set up with a good internet connection. Preferred Qualification: · Candidates currently pursuing a Master’s/Ph.D./Postdoctoral degree in STEM or a related field are eligible and encouraged to apply. · Ability to analyze and solve complex STEM problems with a structured and logical approach. · Ability to explain STEM concepts clearly using simple language, visuals, and simulations when needed. Other Details · Work in a fully remote environment. · Opportunity to work on cutting-edge AI projects with leading LLM companies. · Potential for contract extension based on performance and project needs. · Commitments Required : at least 4 hours per day and minimum 20 hours per week with 4 hours of overlap with PST. (We have 3 options of time commitment: 20 hrs/week, 30 hrs/week or 40 hrs/week) · Engagement type: Contractor assignment/freelancer (no medical/paid leave) · Duration of contract : 1 month; [expected start date is next week] Background Check required Hiring Process Vetting Process:- · The resume should have: the thesis, LinkedIn, and Google publications links mentioned. · Resume Review by TA team. · ICF to be filled by candidate compulsory. · Assessment / MTI as per the Client specifications . · Since there is no interview in the selection process. The resume should hold all the necessities asked for.

Job Description Schweiger Dermatology Group is one of the leading dermatology practices in the country with over 400 healthcare providers and over 170 offices in New York, New Jersey, Pennsylvania, Connecticut, Florida, Illinois, Missouri, Minnesota, and California. Schweiger Dermatology Group provides medical, cosmetic, and surgical dermatology services with over 1.5 million patient visits annually. Our mission is to create the Ultimate Patient Experience and a great working environment for our providers, support staff and all team members. Schweiger Dermatology Group has been included in the Inc. 5000 Fastest Growing Private Companies in America list for seven consecutive years. Schweiger Dermatology Group has also received Great Place to Work certification. To learn more, click here. Schweiger Dermatology Group's Ultimate Employee Experience: • Multiple office locations, find an opportunity near your home, • Positive work environment with the tools to need to do your job and grow, • Full time employees (30+ hours per week) are eligible for:, • Medical (TeleHeath included), HSA/FSA, Dental, Vision on 1st of the month after hire date, • 401K after 30 days of employment, • Your birthday is an additional personal holiday, • Company Sponsored Short Term Disability, • Pre-tax savings available for public transit commuters, • Part-time employees (less than 30 hours) are eligible for:, • Dental and Vision on 1st of the month after date of hire, • 401K after 30 days of employment, • Employee discounts on Schweiger Dermatology Group skin care products & cosmetic services Summary/Objective: A Full Time Grossing Technician at our Pathology Lab in the Financial District. To perform the duties of the Grossing Technician per the Laboratory's Standard Operating Procedures (SOPs). The Grossing Technician will adhere to and support our culture of compliance and safety by following all Standard Operating Procedures (SOPs) with attention to detail, accuracy and professionalism at all times. NYS pathology lab and Mohs clinic providers and staff positions are mandated W-2 employment status positions as required by applicable laws and regulations. Schedule: Monday to Friday 5am to 1:30 pm Essential Functions: Daily essential function of the Grossing Technician are listed below. Details on how each function is to be performed is outlined in the SOP manual. The SOP manual is to be reviewed by all Grossing Technician upon hire, when any updates occur and annually. • Performs tissue description, dissection, and sectioning for optimal diagnostic evaluation of small uncomplicated skin specimens such as shaves, punches and excisions., • Reviews specimens for completeness and accuracy, including site and patient identification., • Selects appropriate processing times and special procedures for tissues (nails, alopecia, hair mounts), • Troubleshoots and resolves technical problems involving methodology, technique, and instrumentation utilization in the gross area/room., • Performs maintenance and quality control on instruments as applicable., • Maintains a safe working environment., • Monitors supply and inventory., • Perform other histology-related work as needed (embedding, microtomy, block/slide filing) once properly trained on all related SOPs prior to completing any work., • Prior work experience of six months is desired in order to gain familiarity on-the-job with histology techniques., • Experience in large-scale organization or high-volume production environment preferred to gain seasoned familiarity with processing specimens in production environment., • Should be familiar with most major techniques for staining and special staining., • Analytical skills necessary for processing slides under tight deadlines and general supervision; should have ability to identify specific specimens for supervisory follow-up., • Completion of a clinical laboratory training program approved or accredited by the ABHES, the CAHEA, or other organization approved by HHS (this training may be included in the 60 semester hours listed in in the education required section) OR at least 3 months documented laboratory training in each specialty in which the individual performs high complexity testing., • An associate degree in a laboratory science, or medical laboratory technology from an accredited institution OR have education and training equivalent to such degree that includes:, • At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either, • 24 semester hours of medical laboratory technology courses; or, • 24 semester hours of science courses that include -, • 6 semester hours of chemistry, • 6 semester hours of biology and, • 12 semester hours of biology and chemistry in any combination Certification is not required for this position (however ASCP HT or HTL Certification is preferred. - Tech II ONLY) Hourly Pay Range$22—$30 USD Schweiger Dermatology Group, is an equal opportunity employer and does not discriminate in its hiring process with applicants, whether internal or external, because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender identity, disability, genetic information, veteran status, military status, application for military service or any other class per local, state or federal law. Schweiger Dermatology Group does not require vaccination for COVID-19 in order to be considered for employment; however, some state guidelines may require that we keep record of your vaccination status on file.

Job Description Excel Sports Management is an industry-leading sports agency representing top-tier talent, blue-chip brands and marquee properties. Our success is rooted in our people, our high character reputation and our commitment to creating a diverse and welcoming workplace. We focus on team chemistry, collaboration, strong relationships, valuable networks, and ambitious ideas to deliver innovative solutions that keep our clients and agency ahead of the curve. Excel Sports Management is an Equal Opportunity Employer (EOE). Position Summary Excel Sports Management is looking for an experienced attorney with a background in employment law to join our burgeoning Legal division. Based in our New York office, you will be responsible for supporting the General Counsel and Operations team with employment related matters. This attorney will take on the critical role of drafting, reviewing and negotiating employment agreements with current and prospective employees. Essential Duties & Responsibilities • Draft and review employment contracts for agency employees., • Advise General Counsel and company on employment law related issues and regulations., • Assist General Counsel and Operations team in the negotiation of employment contracts., • Ensure compliance with national and international labor law, including union regulations (e.g. NBPA, NFLPA, MLBPA)., • Advise company in employment related disputes, arbitration, and litigation., • Monitor changes in employment law and labor regulations., • Provide legal support on immigration matters related to clients or potential employees., • Juris Doctor from an accredited law school., • Admission in good standing to a State Bar, preferably New York or New Jersey., • Expert knowledge of employment law., • Strong drafting, negotiation and analytical skills., • Outstanding organizational skills and an ability to manage strict deadlines., • High level of commitment to quality of work product and organizational ethics, integrity, and compliance., • Strong interpersonal skills and ability to effectively communicate with a wide range of audiences, both written and verbally., • Ability to work independently and collaboratively within a team., • Ability to maintain discretion and confidentiality at all times., • Experience handling litigation, arbitration or mediation in employment disputes., • Knowledge of federal, state and international labor laws., • Expert knowledge in drafting severance, non-solicitation and confidentiality agreements. The pay range for this position is: $100,000- $125,000 per year. This position is also eligible for benefits and discretionary bonus. Please note that the foregoing compensation information is a good-faith assessment associated with this position only and is provided pursuant to the New York City Salary Transparency Law. Ultimately, the salary may vary based upon, but not limited to, relevant experience, time in role, business sector, and geographic location, among other criteria. This position is not eligible for sponsorship. Excel Sports Management provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, leaves of absence, compensation and training.

Job Description Excel Sports Management is an industry-leading sports agency representing top-tier talent, blue-chip brands and marquee properties. Our success is rooted in our people, our high character reputation and our commitment to creating a diverse and welcoming workplace. We focus on team chemistry, collaboration, strong relationships, valuable networks, and ambitious ideas to deliver innovative solutions that keep our clients and agency ahead of the curve. Excel Sports Management is an Equal Opportunity Employer (EOE). Position Summary: The Controller will serve as a proactive and strategic business partner to the CFO—and play an integral role in informing and implementing the strategic, operational, and financial decisions of the company. In this position, you'll be supporting senior management in regards to different growth initiatives including evaluating and integrating M&A, managing the monthly close, monthly financial reporting, and annual audit processes, and overseeing the bookkeeping function including our innovative ERP. The successful candidate will possess thorough knowledge of Generally Accepted Accounting Principles (GAAP), excellent analytical skills, and the ability to execute efficiently to meet company timelines. This position will be based in New York City. Essential Duties & Responsibilities: • Providing strong accounting and financial leadership to inform strategic initiatives, ensure the integrity of the financial statements and adherence to company policies and procedures, • Understanding GAAP and Preparing timely and accurate GAAP financial statements and reports, driven by a tightly managed monthly close process, • GL intercompany and consolidations, • Ensuring the business is structured in a tax-efficient and compliant manner and overseeing the process with external tax preparers with timely and accurate tax filings, • Managing the annual financial audit and serving as the main point of contact with our external auditors for the annual audit, as well as quarterly reviews inclusive of financial statement rollout and footnote disclosures, • Overseeing the ERP to provide accurate records of assets, liabilities and financial transactions, • Developing the long-term vision for the ongoing evolution of financial systems and helping deliver on that vision, • Managing, mentoring and providing a development path for team members, including hiring, training, motivating and addressing performance issue, • 7+ years of relevant accounting experience that includes supervisory responsibilities, • Experience working for a fast-growth company that ideally is backed by private equity or venture capital, • Experience working at a public accounting firm preferred, • M&A experience specifically with auditing and integrating financial systems from multiple exterior companies, • Strong technical accounting experience required, • Process driven; ability to implement and optimize systems, • Previous GL management experience required, • Bachelor's degree in Finance, Accounting or related field. CPA preferred, • Deep knowledge of GAAP, • Strong understanding of tax reporting and compliance, • Experience with progressively increasing responsibility and broader-scale management, including leading a high-performing team and developing leaders from within, • Superb analytical skills, accuracy and attention to detail, • Ability to meet deadlines in a fast-paced environment and manage multiple deliverables/workstreams and delegating to appropriate resources, • Ability to act and operate independently with minimal daily direction, while also possessing a talent for team collaboration, • Good judgment and resourcefulness with the ability to make timely and sound decisions, • Expert proficiency with various accounting software platforms and Microsoft Office (Excel) Please note that the foregoing compensation information is a good-faith assessment associated with this position only and is provided pursuant to the New York City Salary Transparency Law. Ultimately, the salary may vary based upon, but not limited to, relevant experience, time in role, business sector, and geographic location, among other criteria. This position is not eligible for sponsorship. Excel Sports Management provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, leaves of absence, compensation and training.

Job Description Excel Sports Management is an industry-leading sports agency representing top-tier talent, blue-chip brands and marquee properties. Our success is rooted in our people, our high character reputation and our commitment to creating a diverse and welcoming workplace. We focus on team chemistry, collaboration, strong relationships, valuable networks, and ambitious ideas to deliver innovative solutions that keep our clients and agency ahead of the curve. Excel Sports Management is an Equal Opportunity Employer (EOE). Position Summary: The primary responsibility of this position is to develop integrated sponsorship platforms and proposals for teams, leagues, rightsholders, and major brands. This individual will serve as a central hub for idea generation and brand storytelling, while working with the respective salesperson(s) to bring a deal from introductory call to close. The ideal candidate will be able to intuitively understand a brand's objectives, identify an authentic alignment, develop a narrative, integrate impactful insights, customize a comprehensive platform, and oversee the creative development of all deliverables. A comfort with copywriting is also essential to success in this role. With a true attention to detail, this individual will be tasked with writing, proofreading, editing, and providing constructive feedback to teammates on a daily basis. This role can be based in either our New York or West Hollywood offices. Essential Duties & Responsibilities: • Works collaboratively with our clients, leadership, sales executives, creative services, analytics, and other key departments to manage and develop the sales materials required for every project;, • Leads the creative ideation process for properties and brand partners, in conjunction with the sales and creative teams, developing customized sponsorship platforms and packages based on the property characteristics and the priorities of the prospect;, • Builds narratives/storylines for corporate sales opportunities and structures impactful presentations;, • Writes, reviews, and proofreads proposals, presentations, and other documents with extraordinary attention to detail, consistency, and grammar;, • Participates in client-facing meetings, business development pitches, and brand presentations with confidence, comfort, and ease, as needed;, • Organizes team workflows and timelines, while managing up to team leaders on priorities;, • Identifies new tools and efficiencies to benefit the marketing solutions team and optimize the quality and speed of materials developed for the properties sales team;, • Collaborates with team members at all levels, serving as an essential resource across the division;, • Invests in both personal growth and development, while serving as a champion to grow peers and junior team members. Education & Experience: • Bachelor's degree required;, • At least 7+ years of direct, relevant work experience;, • Proven ability to be a project lead for multiple projects/clients simultaneously;, • Experience managing individuals with the ability to inspire their growth and development;, • Client-facing experience or a project management background is a plus. Knowledge, Skills and Abilities: • Demonstrated ability to work in a highly-collaborative environment;, • Clear and effective copywriting and proofreading abilities, with high attention to detail;, • Excellent presentation and verbal communication skills;, • Ability to manage multiple projects while being responsive to the needs of the division and peers, be able to prioritize effectively and exercise flexibility as needed;, • Self-confidence in both brainstorm organization and individual idea generation;, • Excellent project management, organization and administrative skills;, • Knowledge and understanding of sports and entertainment industries;, • Strong research and analytical skills, with the ability to tell a story through data;, • Ability to identify and solve problems creatively;, • Self-motivated and self-directed;, • Positive outlook and culture builder;, • Highly responsive and accessible, with the flexibility to work nights and weekends if needed. The pay range for this position is: $115,000-$130,000 per year. This position is also eligible for benefits and discretionary bonus. Please note that the foregoing compensation information is a good-faith assessment associated with this position only and is provided pursuant to the New York City Salary Transparency Law. Ultimately, the salary may vary based upon, but not limited to, relevant experience, time in role, business sector, and geographic location, among other criteria. This position is not eligible for sponsorship. Excel Sports Management provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, leaves of absence, compensation and training.

Job Description Cresilon® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company’s proprietary hydrogel technology. The company’s plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure. The company's current and future product lines target veterinary, human trauma, and human surgical applications. Cresilon's mission is to save lives. Learn more about the company at . The Preclinical Principal Scientist will serve as a key scientific contributor, subject matter expert (SME) and Project Manager in the execution of Cresilon’s Preclinical Research Operations, including but not limited to in-vivo study design (Safety and Efficacy/Functionality evaluations), Preclinical Research Management, Vendor Management, and Preclinical Regulatory Strategy. This will include the development and execution of strategies for preclinical evidence necessary to competitively position a project’s product for domestic and international regulatory and clinical acceptance. This position as a hybrid role, with work off-site at CRO in NY/NJ area, work from home and on-site at Brooklyn NY. Job Responsibilities: The Preclinical Research Scientist will: • Lead, staff, and manage Cresilon’s Preclinical Research activities., • Provide preclinical scientific input and leadership on the evaluation of physical safety and efficacy for technologies and products at all stages of the product life cycle., • Plan, direct, coordinate and execute activities related to the design, initiation and follow-up of studies to support approval of Class I-III medical devices., • Develop, write, and/or review study protocols and reports. Act as technical mentor for the development of study experimental designs, protocols, and reports of junior associates., • Administrate and manage Cresilon preclinical regulatory strategy and communication., • Work with Contract Research Organizations (CROs) to execute both Biocompatibility / Safety and Efficacy/Functionality research, including negotiating, drafting, and managing research contracts and agreements with pre-clinical trial sites., • Ensure that company operates within the scope of regulatory compliance including Quality System Regulations (ISO 13485), health and safety, environmental protection regulations, and the core values of Cresilon., • Be a Subject Matter Expert (SME) for preclinical research department growth strategy. Actively interact with the internal and external scientific community to maintain state of the art knowledge., • Oversee the development of and modifications to preclinical models to address project needs., • Oversee the design and execution of preclinical functionality and safety in-vivo studies per project timelines., • Surveys the literature to identify and compare competitive product performance and safety risks., • Maintain current knowledge in existing regulations, requirements and standards, including but not limited to global regulatory requirements (ISO, FDA, etc) and compliance requirements (GLP, USDA, AAALAC, departmental SOP's, company policies, etc), • Work cross functionally with Regulatory and Quality to assess project risks, product safety and efficacy on NPD projects, including ensuring external facilities meet Cresilon standards for animal use and generating contracts and CRO audits, if necessary., • Manage budgetary requirements for all research projects to support efficacy and safety programs., • Lead the effort to publish surgical research in peer-reviewed journals., • Regularly interface with management to ensure research operations reflect overall corporate vision/strategy., • DVM, PhD or MD in a relevant discipline is preferred, A Bachelors in a technical or scientific field is required., • Minimum 6+ years’ experience in preclinical medical device research is required, preference given to veterinary surgical experience., • 4+ years of people management experience preferred., • Extensive knowledge of surgery, anatomy, toxicology, and pathology is required., • Experience with planning, directing, and coordinating activities related to studies to support approval of Class I-III medical devices is highly preferred., • Experience in a medical device, pharmaceutical, or related setting with a proven record of success in supporting studies for R&D projects is highly preferred., • Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare Regulations., • Experience with surgical publication submission strategy is strongly preferred., • Strong communication skills (both written and verbal) is required with the ability to extract key facts from complex information and present concise summaries to management., • Demonstrated experience with large animal in vivo surgical research and CRO vendor management is required., • Previous experience in authoring and reviewing nonclinical regulatory documents as well as interactions with regulatory authorities is strongly preferred., • Excellent problem solving, conflict resolution, and analytical skills is required., • Ability to work effectively both independently and collaboratively in a dynamic team-oriented environment is required., • Prior experience and ability to work well with external CROs and collaborators with professionalism and discretion is required., • Requires strong leadership and organizational skills including attention to detail and multi-tasking skills., • Able to understand and execute to project details but keep overall “big picture” view of projects, priorities, and strategies is required., • Medical Device product development experience, including knowledge of medical device regulations, regulatory/notified body requirements is preferred., • Good Laboratory Practices (GLP) experience preferred and working knowledge of Good Manufacturing Practices (GMP), • Experience in developing and commercializing regulated devices under Design Control (21 CFR 820) requirements, GLP/GMP, and ISO regulations is preferred., • Hands-on research experience with hemostatic devices and/or coagulation chemistry, strongly preferred., • Legal authorization to work in the United States., • This position is located in Brooklyn, NY and may require up to 30% travel (to monitor and execute out-sourced studies) Cresilon is an equal-opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Cresilon makes hiring decisions based solely on qualifications, merit, and business needs at the time. Benefits • Competitive annual base salary range of $130,000 - $210,000, depending upon job level and qualifications., • Paid Vacation, Sick, & Holidays, • Medical, Dental, and Vision Insurance, FSA: Dependent & Healthcare, Commuter & Parking Benefits, Long Term Disability Coverage, • Company Paid Life and Short-Term Disability Coverage, • Work/Life Employee Assistance Program, • Monthly MetroCard Reimbursement, • 401(k) & Roth Retirement Savings Plan with company match up to 5%

Job DescriptionSalary: $22-$25 DOE Job Summary: We are seeking a motivated and detail-oriented R&D Lab Technician to join our team. This position plays a key role in supporting product development tasks, including executing bench-top formulations across various specialty food product categories. In this fast-paced R&D environment, the technician will ensure accurate sample preparation, data collection, and adherence to project timelines. Key Responsibilities: • Maintain a clean, safe, and organized R&D lab by following established procedures., • Prepare benchtop samples for internal evaluations, consumer testing, and sales presentations., • Conduct shelf-life testing on prototype and finished products., • Manage inventory of lab ingredients and supplies., • Collect and document analytical data on new and existing formulations., • Operate lab, kitchen, and plant equipment as needed., • Ensure accurate and timely sample preparation to meet project timelines., • Adapt to changing priorities and work efficiently under deadlines., • Perform additional duties as assigned. Education & Experience Requirements: • Bachelors degree in a science-related field with hands-on benchwork experience., • Prior experience in food science, product development, or a related field preferred., • Ability to execute benchwork accurately and communicate findings effectively., • Strong organizational skills and attention to detail., • Excellent written and verbal communication skills., • Ability to manage multiple projects simultaneously with precision., • Comfortable in fast-paced and dynamic environments., • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)., • Strong math skills for calculations and data analysis. Preferred Skills & Qualifications: • A process-driven mindset with a commitment to continuous improvement., • Strong critical thinking and problem-solving skills., • Excellent interpersonal skills and a positive, team-oriented attitude., • Experience with wet chemistry lab techniques is a plus., • Experience in manufacturing environments is an advantage. PANOS Brands makes great-tasting, better-for-you foods enjoyed by millions of households every year. Based in the New York City area, PANOS stands for Premium, Authentic, Natural, Organic and Specialty the characteristics of our brands that set us apart within the food industry. Our portfolio includes family-favorite foods and ingredients, including KA-ME Asian Noodles & Cooking Sauces, Andrew & Everett Cheese, Walden Farms and Tessemaes Salad Dressings, Santa Barbara Smokehouse Smoked Salmon, Amore Tomato Paste, MI-DEL Ginger Snap Cookies and Gluten-free Pie Crusts, and Sesmark Crackers. Join us and be part of a dynamic team dedicated to winning through collaboration, with a culture where individuals can flourish. Join us and be part of a dynamic team dedicated to winning through collaboration, with a culture where individuals can flourish!

Job Description PerkinElmer has partnered with Hueman to find a Full-Time Field Service Engineer in Long Island, NY. The Field Service Engineer provides highly visible customer support through the performance of on-site installation, as well as overseeing any necessary diagnoses, troubleshooting, service, and repair of complex equipment and systems. The Field Engineer will instruct customers in the operation and maintenance of the system and serve as company liaison with customer on administrative and technical matters for assigned projects. This role may include any aspect of field support, and is not limited to system hardware and software, PCs, and networking/wireless networking. PerkinElmer is a leading, global provider of technology and service solutions that help customers measure, quantify, detect, and report in ways that help ensure the quality, safety, and satisfaction of their products. For 85 years, PerkinElmer has pushed the boundaries of science in our food, industrial, life science and environmental markets. In addition to innovative laboratory technologies, our OneSource services division delivers a highly trained, experienced, and collaborative team of service engineers with solutions scalable and customizable to serve laboratory needs. Job Responsibilities: • Perform installations, maintenance, validations, and repairs while ensuring compliance with PerkinElmer’s service standards and key performance indicators, • Engage with customers to understand their analytical workflows and tailor service offerings, including training, support, and upgrades., • Enhance account profitability through efficient service execution and by identifying revenue opportunities such as billable work, consumables, and service leads, • Maintain assigned assets, including tools, test equipment (MTE), telecommunication equipment, and service parts inventory., • Enhance PerkinElmer’s product quality by proactively reporting improvement opportunities via the quality notification process., • Attend higher level certification through participation in company sponsored training & development offerings, • Complete all administrative tasks, including but not limited to time reporting and assigned training., • BA Bachelor Degree in Applied Science, Biology, Chemistry, Electronics, Mathematics, Engineering, or related discipline including military experience plus 3 years direct experience with repair of laboratory equipment OR, • Associate Degree in Applied Science, Biology, Chemistry, Electronics, Mathematics, Engineering, or related discipline including military experience plus 5 years direct experience with repair of laboratory equipment OR, • High School Diploma plus 7+ years direct experience with repair of laboratory equipment, • Outstanding interpersonal, written, and verbal skills, demonstrating the ability to communicate information clearly and accurately., • Technical critical thinking skills and attention to detail., • Outstanding customer service skills complemented by an ability to listen to and interpret client requests., • Aptitude for technical and practical matters., • MS Office skills: Outlook, PowerPoint, Word., • Excellent team player with a customer satisfaction focus, • Ability to follow and create written and verbal directions, read and understand technical bulletins and service manuals, work under time constraints, maintain alertness and concentration, and work safely with potential hazard Preferred Qualifications: • Detailed knowledge of analytical equipment, laboratory environment, and/or instrument control software, • Vendor issued certification on relevant laboratory equipment, • Knowledge of laboratory safety practices as defined by the Company and/or the customer’s site safety code, • Ability to travel by air, vehicle and/or other means of transportation as business requires. Travel will vary depending on territory requirements and/or customer base typically up to 50% of the time. (Car, laptop, and phone are company provided)., • Valid driver’s license and safe motor vehicle operation. AT PERKINELMER, WE BELIEVE IN THE POWER OF SCIENCE TO TRANSFORM OUR WORLD We partner with scientists, clinicians, lab technicians, engineers, and food producers globally to empower them with reliable and compelling scientific insights they need to accelerate the development of ground-breaking products, and laboratory solutions that improve the quality of our lives. By drawing on the ingenuity, creativity, and passion of our people, together, we enable our customers to fulfil their mission towards a healthier, safer, and more sustainable world. Hueman is proud to partner with PerkinElmer as the exclusive recruitment partner for this role. If you are interested in learning more about a career with PerkinElmer as a Field Service Engineer, apply today!

Job DescriptionWho we are… Nuvation Bio is a biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates. Our vision is to significantly change the practice of oncology by developing medicines that provide truly meaningful improvements in quality of life and survival for people with cancer. What you’ll be doing The Senior Clinical Trial Manager will be responsible for the operational management and oversight of clinical trials, sites, and vendors within a clinical development program. This role works closely with the Clinical Operations team as well as other key cross-functional team members to ensure that Nuvation Bio conducts high quality clinical trials efficiently, cost effectively, and in alignment with corporate deliverables and timelines. Additional accountabilities may include collaborative development of program level operational strategy, budget projections, and day-to-day personnel management and development as needed. You will be responsible for… • Plan and organize the implementation of clinical studies to ensure that the studies are delivered on time, on budget and to quality as expected from planning, initiation, implementation, to completion., • Develops and track quality and risk management plans for clinical studies, organizes feasibility studies at the study, country and/or study center level, identifies participating countries and/or study centers, and develops subject recruitment strategies., • Responsible for the preparation of clinical operation related documents, including clinical study required documents, ethics committee review materials, genetic resources related filings, and domestic and international clinical trial disclosures., • Organize investigator/monitor meetings and ensure that they receive adequate and appropriate training, • Develop clinical monitoring plans and oversee their implementation and ensure the quality of clinical monitoring through co-monitoring or other means., • Organize clinical study teams and identify appropriate external vendors., • Plan and manage clinical study budgets., • Organize regular internal and external meetings to maintain oversight of internal deliverables and external vendors., • Regularly review clinical trial required documents to ensure their completeness and filing in the Trial Master File within the required timelines., • Regularly report on study progress, milestones, and major risks and issues.What Knowledge & Experience you'll bring to us..., • Minimum Educational Requirement:, • Bachelor’s Degree preferably in Life Sciences (e.g. Biology, Chemistry, Pharmaceuticals), Business Administration or related discipline or equivalent experience., • Experience:, • At least 5 years experience managing or supporting clinical trials and/or directly applicable experience in drug development, ideally includes a small, start-up environment., • Oncology experience preferred., • Experience managing clinical trials staff directly or indirectly desirable., • Core Competencies:, • Direct, prior experience with selecting and managing CROs and other key vendors., • Direct, prior experience with multiple phases of clinical trials including start-up, enrollment, maintenance, and close-out., • Current knowledge and understanding of FDA, CFDA, and ICH Guidelines, including Good Clinical Practices (GCP) E6(R3) requirements., • Proficient with MS Word products and database software; experience in directly using electronic data capture., • Familiarity with drug development processes across all phases of development (early to late stage)., • Travel may be required for clinical investigative site visits, vendor visits, meetings, and presentations., • Communication & Interpersonal Skills:, • Excellent communication and interpersonal skills., • Must be able to write clearly and summarize information effectively., • Must be self-motivated and able to prioritize/manage a large volume of work in a dynamic, changing, growing start-up culture., • Must be able to present complex information to various audiencesBehavioral skills to be successful..., • Problem-Solver - As an action-oriented self-starter, you’re eager to apply your expertise in diagnosing inefficiencies, determining root causes, and recommending solutions to complex challenges., • Personable - You establish and nurture highly effective relationships with colleagues and key stakeholders that support and advance project goals and objectives., • Credible - Thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource., • Emotional intelligence, curiosity, and a knack to figure out a way to build something better, • Communication - Effectively listens, conveys, and receives ideas. Maintains a consistent flow of information. A strong presenter and effective communicator with the ability to influence stakeholders., • Accountability - Acts with a clear sense of ownership - whether the task is in their role description. Holds yourself and others accountable to execute all tasks at hand through seen and unforeseen circumstances with high quality and integrity., • Adaptability - Can manage in an environment of ambiguity. Embraces the change of a new system, process, technology, or idea in the organization. You could reassess priorities, alter goals and take risks.What we have for you!, • Competitive Base Salary, Bonus, and Equity Plans, • Unlimited Vacation and 10 Sick Days Annually, • Excellent Medical, Dental, and Vision Coverage, • 401K with Company Matching Disclaimer Nuvation Bio, Inc. is an equal opportunity employer, and, in accordance with applicable federal, state, and/or local law, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by the law. This job description reflects the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Nothing restricts management’s right to assign or reassign duties and responsibilities to this job at any time. Note to all external Recruiters & Staffing Agencies All of our open positions are managed by our Talent Acquisition department. Any resumes submitted through the website or directly by recruiters or staffing agencies in advance of an executed agreement with Nuvation Bio, Inc., will be considered unsolicited and the company will not be responsible for any related fees. Resumes sent directly to employees or hiring managers will also not be accepted as referrals.

Job Description About Atria: Atria is a membership-based preventive health care practice delivering cutting-edge primary and specialty care from the comfort of your home, at our practices in Palm Beach and New York, or wherever you are in the world. We bring together a multidisciplinary team of renowned, in-house physicians to provide proactive, preventive, and precision-based care for Atria members and their families. We aim to optimize the lifespan and healthspan of all our members through meticulous screening and tailored interventions to prevent, reverse, or manage all major chronic diseases. Each member’s care is led by a dedicated Chief Medical Officer who collaborates on your behalf with specialists in cardiology, neurology, pediatrics, gynecology, endocrinology, performance and movement, and more. Our exceptional clinicians also work closely with the 60+ members of the Atria Academy of Science & Medicine, top experts in their respective fields who are available for rapid consults, support, and referrals. About the Role: Atria is seeking a Laboratory Supervisor for our in-office laboratory in Manhattan. This position will oversee the collection, processing, and testing of in-office orders of waived and moderate complexity assays, interaction with partner labs for send-out of high complexity testing, and maintain of the laboratory with a focus on compliance and safety. The position is on-site during business hours on weekdays with occasional need for additional coverage due to clinical and business needs. We are looking for an energetic and motivated leader with a passion for quality, continual improvement, and delivering exceptional clinical care. Experience: Minimum of 6 years in a high complexity clinical laboratory with experience in Hematology and Chemistry required. Experience with waived and moderate laboratory operations is desired. The ideal candidate has experience with phlebotomy and patient facing care. Key Responsibilities: • Provide day-to-day technical and regulatory oversight of the laboratory, • Ensure compliance with CLIA and NYS DoH regulations and standards, • Verify test procedures and monitor performance criteria, including accuracy and precision, • Enroll and participate in proficiency testing programs, • Maintain and employ the quality control program, • Resolve technical problems and ensure corrective actions are taken, • Identify training needs and ensure regular in-service training for testing personnel, • Evaluate the competency, proficiency, and confidence of all testing personnel, • Oversee the process of collection, preparation, and submission of testing to external partner labs, • Prepare samples and perform waived and moderate complexity testing, • Maintain inventory and interact with purchasing and finance as needed Compensation: $95,000 - $115,000 Requirements • Extensive documentation experience, including maintenance of records, the creation of forms and documents to support operations, and a record of review/audit experience, • Practiced and successful history of problem resolution through Root Cause Analysis (RCA), Corrective and Preventive Actions (CAPA), and Change Management, • Demonstrable capabilities as a bench tech in Hematology and Chemistry, • Deep understanding of test orders, requisitions, specimen preparation, accessioning, and data flows from LIMS to EMR, • Strong analytical and problem-solving skills, • Excellent communication and interpersonal skills, • Current NYS CLT license is required or able to be obtained., • Certification with ASCP or similar is a preferred., • Bachelor's degree in Biological or Chemical sciences, Clinical Science, or related field. At Atria, we are proud to offer every member of the Atria team: • Excellent health and wellness benefits, 100% paid by Atria effective date of hire, • Flexible Time Off, • 401k match at 4% effective 6 months after date of hire, • Opportunity to participate in continuing medical education programs for maintenance of Continued Medical Education and CEUs for professional licensure, • Fitness Perks including Wellhub +, • Time to give back and make an impact in underserved communities

Job Description Clinical Testing Company seeks Medical Laboratory Scientist who will be responsible for performing routine and non-routine activities pertaining to laboratory testing and the reporting of results. Shift: Monday - Friday 9:00 AM - 5:30 PM Will perform moderately difficult to complex tasks and will perform assigned analytical testing procedures in an accurate, precise, and timely manner. JOB RESPONSIBILITIES: • Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result;, • Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens;, • Analyze specimens using approved testing procedures (see department SOPs)., • Review and release test results., • Follow CLIA, HIPAA, OSHA, and safety guidelines as described in their respective guidelines., • Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and all maintenance performed;, • Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance., • Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor., • Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications., • Follow department's procedure in reporting STATS or Critical results to clients., • If applicable, answer questions from customers or other lab personnel., • Maintain complete records of all testing performed on-site., • Maintain general appearance of the department., • Make sure reagents/test kits have received dates, expiration dates, and if applicable opened dates. 15. Review/train on new procedures., • Attend monthly department and any additional training/educational meetings., • Participate in all applicable safety training sessions. Know the location and contents of the safety manual. Know the location/use of all applicable safety equipment., • If needed, participate in government or regulatory agency inspections., • A solid understanding of basic laboratory testing is required for this position. The successful candidate must possess good computer skills and be able to adapt to working in multiple computer systems., • BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or, • Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990., • Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)., • United States educated candidates must provide a detailed original transcript., • 1 year Clinical experience (high complexity testing) preferred., • Minimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology., • Must have the ability to establish work priorities and handle several procedures simultaneously., • Must interact with other departments., • Contact with clients may be required, good customer service skills are important.

Job DescriptionSupplier Quality AuditorAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Device, IT & Human Resources disciplines in New Jersey. The Supplier Quality Auditor ensures and promotes compliance through external auditing of company's suppliers; vendors/ laboratory services/service providers/manufacturers for the Allendale, NJ and Mountain View, CA sites based on company's procedures and external regulatory requirements, including but not limited to current FDA Quality System Regulations; 21 CFR Parts 210/211 (cGMP), 21 CFR Part 1271 (GTP), 21 CFR Parts 50/54/56/312 (GCP), 21 CFR Pat 58 (GLP), ICH Q7, Q9, Q10, 21 CFR Part 11 and Data Integrity and Eudralex Volume 4 Guidelines.The Supplier Quality Auditor position will be responsible for the development of a risk-based auditing program for company and management of the Approved Supplier List. The Supplier Quality Auditor will conduct external supplier/vendor/manufacturer audits and harmonize the supplier qualification process across all sites. The Supplier Quality Auditor supports qualification initiatives, continuous improvement, and regulatory compliance across all sites. • Develop and maintain a risk-based external auditing program for company harmonized across all sites., • Perform GAP analyses of the Approved Supplier List (ASL) of suppliers used at all company facilities to ensure complete profile., • Management of ASL to add suppliers and maintain approval status of all suppliers as needed., • Based on ASL status, conduct reviews and perform audits to qualify each supplier used., • Prepare external audit schedule and conduct audits per the schedule., • Prepare and complete audit reports and communicate audit information to cross functional teams within company and supplier within a timely manner., • Ensure adequate CAPAs are developed by suppliers and monitor CAPA closures., • Track audit findings for suppliers to completion and ensure timely closure of audit reports., • Act as a quality lead and liaison between suppliers and internal teams to identify new suppliers and identify and communicate issues that may impact quality, system gaps or cause interruptions in business continuity., • Maintain metrics on supplier audit findings used for oversight, qualification status, continuous improvement, and/or opportunities for reduction/alternate suppliers., • Maintain audit files and ensure all files are properly archived., • Author and review External Auditing, Supplier Qualification and Supplier Management Program and/or Quality Systems SOPs, as needed., • Ensure that Quality Agreements are generated and enforced at each supplier., • Ensure and promote compliance with applicable regulations (e.g., cGMPs, GTPs, etc.) and company and client SOPs., • Assist in other Quality System related responsibilities and provide Quality related support to various departments, as needed.REQUIREMENTS, • Minimum 5-8 years quality systems auditing experience in pharmaceutical, biologics, or medical device industry., • Auditor qualifications and certifications such as Certified Quality Auditor (CQA)/ASQ Certification, ISO Certification, etc., • Experience with auditing raw materials/excipients, components, and analytical and micro laboratories., • Proven ability to identify, collaborate, and resolve supplier related compliance issues., • In-depth knowledge and understanding of current Good Manufacturing Practices (cGMPs), Good Laboratory Practices (GLPs), ICH Q10, 21 CFR Part 11, Good Tissue Practices (GTPs) and Data Integrity principles,, • EU and PMDA regulations knowledge and associated guidelines are a plus., • Bachelor’s Degree in the chemistry or biological sciences, engineering, or life sciences., • Certified Auditor or Lead Auditor credentials required., • Understanding of the manufacture and testing of cellular and gene therapies is desirable., • Working knowledge of routine laboratory operations, equipment and systems, production processes, and validation., • Experience in Quality Assurance, including the ability to identify and resolve compliance issues., • Sound knowledge of aseptic processing and supporting technologies., • Must have exceptional written and oral communication skills., • Exhibit professional mannerisms when dealing with Clients/Suppliers and company personnel, • Ability to multi-task is essential., • Proficiency with IT skills, such as MS Office (Word, Excel, Outlook, PowerPoint) and SharePoint., • Ability to think strategically and tactically (strong detail-oriented)., • Strong collaborative and influencing skills and ability to work well in a cross-functional, team matrixed environment as well as independent contributor., • Strong analytical and problem-solving skills., • Flexible and able to adapt to company growth and evolving responsibilities., • Multi-disciplinary knowledge across GxP functional areas., • Excellent organizational skills including efficiency, punctuality and attention to detail and managing multiple priorities., • Good verbal, written communication, and presentation skills., • Demonstrable multitasking, project management, and execution skills., • Good business acumen and strong team-oriented interpersonal skills, including communication, presentation, negotiation, influence., • Environment includes working with all levels of internal management and staff as well as with external clients, suppliers, and contractors., • Must have the ability to work in a team-oriented environment and with clients, • Must be able to handle the standard/moderate noise of the manufacturing facility, • Travel required (approx. 50%)Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Job DescriptionSalary: Base salary range $62,500 - $67,000 Corporate Insight (CI) is a research and consulting firm known for providing actionable competitive intelligence on the digital customer experience. CI publishes in-depth research on online/mobile banking, investing, insurance, retirement, healthcare and emerging areas like fintech and digital advice. For 30 years, we have helped firms improve the way they serve millions of customers by offering objective feedback and advice on their customer experience. CIs clients include approximately 70% of the financial services firms in the Fortune 500. CI is looking for talented and motivated Research Associates to join our Projects Team. Research Associates support our Analysts, Senior Analysts and Project Managers in conducting custom research projects for clients with a focus on consumer financial services. Typical engagements involve benchmarking a client firms website or app versus competitors, identifying industry best practices and key trends, and providing advice to help the client improve the overall experience they provide to their customers. The Research Associates chief responsibility will be to contribute to team-based projects by performing detailed research and analysis, collecting competitive intelligence and collaborating on written reports and presentations to clients. Successful Research Associates grow into Analysts and then Project Managers, developing deep industry/subject matter expertise, the ability to lead large research engagements, superb presentation skills and the ability to manage relationships with clients throughout the full project lifecycle. CI strives to deliver high-quality work daily, but we like to have fun, too. Our active social committee organizes regular team-building and recreational events. We have frequent in-office, out-of-office and hybrid events, including field days, scavenger hunts, board game tournaments, an annual Yankee game, and more. CI provides health, vision and dental insurance, and a 401(k) with a company contribution. We also provide paid time off: vacation days, sick days and personal days. CI is currently operating on a hybrid model at our NY office where team members will be expected to work at our Midtown Manhattan office part of the time. Unfortunately, we are not able to sponsor visas for this position. SpecificResearch Associate responsibilitiesinclude: * Supporting Analysts, Senior Analysts and Project Managers on client engagements, with a focus on collecting competitive intelligence on the digital experience * Conducting primary research on assigned topics and writing detailed findings * Developing well-supported and actionable recommendations to help our clients address unique business challenges * Contributing to executive summaries and presentations to debrief clients on project results * Managing multiple project-related tasks simultaneously This position is suited for an entry-level candidate interested in beginning a career in business, consulting, research, or financial services. Your cover letter should outline your qualitative research, writing, and project management experience. Successful applicants have a range of backgrounds, including but not limited to business, economics, English, history, chemistry, government, and sociology. Note: This is not a financial analyst position.Candidates with experience that exceeds the below may be hired at a more senior level. Requirements include: * Bachelors degree and a record of strong academic performance * Exceptional writing, speaking, and analytical skills * Positive attitude, strong work ethic, and intellectual curiosity * Professional writing style with experience writing in multiple styles * Experience working independently and collaborating with a team * Experience conducting research and communicating results to an audience • Leadership experience Attention to detail and the ability to synthesize information to arrive at clear and useful insights * Ability to handle multiple research projects simultaneously and maintain excellent work quality under tight deadlines Preferred qualifications include: * Experience working in a business environment (internships in market research, financial services or consulting are a plus) * An understanding of both website usability principles and personal finance * Quantitative research experience, specifically survey data analysis * Experience working with Microsoft Office (familiarity with SharePoint and OneDrive is a plus) Corporate Insight 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

Job Description Key Responsibilities: 1. Formulation Development: o Develop and optimize pest control formulations, including insecticides, rodenticides, repellents, and larvicides. o Tailor formulations to meet efficacy, safety, environmental, and regulatory requirements. 2. Product Testing and Evaluation: o Conduct laboratory and field tests to evaluate product effectiveness against target pests. o Assess physical and chemical stability, efficacy, and environmental impact under various conditions. 3. Regulatory Compliance: o Ensure formulations comply with local, national, and international regulatory standards (e.g., EPA, EU regulations). o Prepare and submit technical documentation for regulatory approval. 4. Research and Innovation: o Explore and integrate emerging active ingredients, delivery systems, and sustainable practices into product development. o Stay informed about new technologies and advancements in pest control chemistry. 5. Process Improvement: o Collaborate with manufacturing teams to scale up formulations and optimize production processes. o Troubleshoot issues during scale-up and recommend improvements for quality control. 6. Documentation and Reporting: o Maintain accurate lab records, including experimental design, data analysis, and findings. o Prepare detailed technical reports and present research results to internal and external stakeholders. 7. Collaboration and Teamwork: o Work with cross-functional teams, including biology, regulatory, and marketing teams, to ensure product success. o Liaise with suppliers and external research organizations as needed. Qualifications: Education and Experience: • Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Agricultural Science, or a related field., • 2+ years of experience in pesticide formulation, pest control product development, or related fields preferred. Technical Skills: • Strong knowledge of pesticide chemistry, toxicology, and modes of action., • Experience with analytical techniques such as HPLC, GC-MS, or FTIR for active ingredient analysis. • Familiarity with encapsulation, emulsification, and other delivery technologies. Soft Skills: • Excellent problem-solving and analytical thinking abilities., • Strong written and verbal communication skills., • Ability to work effectively in a team-oriented and fast-paced environment. Preferred Qualifications: • Experience with biodegradable and environmentally friendly pest control solutions., • Knowledge of integrated pest management (IPM) practices and their implementation. We’re proud of the investments we’ve made in our team, having grown from four to 1000 employees and evolving into one of the leading recruitment and staffing solution providers in the industry. Our recruiters and account managers are passionate about connecting qualified professionals with the right positions in small, medium, and large companies. Our Services W3Global understands the natural ups and downs of an organization’s staffing needs. We are continuously adapting to industry and economic changes to find the right candidates. We specialize in placing permanent, direct, contract, and temporary positions for companies of any size. Our recruiting services include sourcing, recruiting, screening, interview management, salary negotiations, training, and onboarding. We are committed to helping organizations redefine their recruitment process by delivering our SaaS-based proprietary application tracking system software. Our Expertise W3Global has been delivering staffing solutions for nearly two decades; we know which recruiting strategies work best. Our expert team is committed to developing a customized solution to fit your company’s unique needs. As a W3Global client, you’ll also receive personalized assistance from a seasoned team of staffing specialists. We are committed to providing both technical support and industry expertise to simplify the hiring process. We know that your time matters. W3Global will help you streamline the hiring process, getting it done and getting it right.W3Global was established in 2006 in Fremont, CA with a vision: simplify the recruiting process and develop an industry-disrupting platform to connect candidates with clients. Our cutting-edge Applicant Tracking System enables us to find the right person for the right job, creating value for job seekers and employers. While W3Global initially focused on IT staffing, we have expanded the business to serve many other industries, including accounting and finance, legal, engineering, human resources, government and more.\r\n\r\nWe’re proud of the investments we’ve made in our team, having grown from four to 1000 employees and evolving into one of the leading recruitment and staffing solution providers in the industry. Our recruiters and account managers are passionate about connecting qualified professionals with the right positions in small, medium, and large companies.\r\n\r\nOur Services\r\nW3Global understands the natural ups and downs of an organization’s staffing needs. We are continuously adapting to industry and economic changes to find the right candidates.\r\n\r\nWe specialize in placing permanent, direct, contract, and temporary positions for companies of any size. Our recruiting services include sourcing, recruiting, screening, interview management, salary negotiations, training, and onboarding.\r\n\r\nWe are committed to helping organizations redefine their recruitment process by delivering our SaaS-based proprietary application tracking system software.\r\n\r\nOur Expertise\r\nW3Global has been delivering staffing solutions for nearly two decades; we know which recruiting strategies work best. Our expert team is committed to developing a customized solution to fit your company’s unique needs.\r\n\r\nAs a W3Global client, you’ll also receive personalized assistance from a seasoned team of staffing specialists. We are committed to providing both technical support and industry expertise to simplify the hiring process. We know that your time matters. W3Global will help you streamline the hiring process, getting it done and getting it right.

Perform basic chemistry tasks such as pipetting, volumetric measurements, and the utilization of analytical balances. Laboratory Technician II (Chemistry). Operate and maintain basic analytical equipment and instruments.

TotalMed Allied is seeking a travel Cath Lab Technologist for a travel job in Rochester, New York.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 09/15/2025 Duration: 17 weeks 40 hours per week Shift: 8 hours, days Employment Type: T

David creates tools to increase muscle and decrease fat.Our first product is a protein bar.More broadly, David is a platform to develop high-protein, low-calorie, blood-sugar-friendly foods that are craveable.This is a compelling opportunity to be a part of an exciting new food brand as we operate w

Host Healthcare is seeking a travel Cath Lab Technologist for a travel job in New York, New York.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 09/23/2025 Duration: 9 weeks 38 hours per week Shift: 8 hours, evenings Employment Type:

Combining our leading positions in the science of materials flow, surface modification, and formulation with access to unique natural materials, Elementis delivers unique chemistry, sustainable solutions to customers in a wide range of markets, including cosmetics, anti-perspirants, decorative and i

PRIDE Health is seeking a travel Cath Lab Technologist for a travel job in Rochester, New York.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: ASAP Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel A

David creates tools to increase muscle and decrease fat.Our first product is a protein bar.More broadly, David is a platform to develop high-protein, low-calorie, blood-sugar-friendly foods that are craveable.This is a compelling opportunity to be a part of an exciting new food brand as we operate w

PHP is seeking a travel Cath Lab Technologist for a travel job in Rochester, New York.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 09/15/2025 Duration: 13 weeks 40 hours per week Shift: 10 hours Employment Type: Travel PHP Job ID

Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life.Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory.This foundational understanding of smell's imp

Host Healthcare is seeking a local contract Cath Lab Technologist for a local contract job in New York, New York.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 09/23/2025 Duration: 9 weeks 38 hours per week Shift: 8 hours, evenings

The Biology Department is seeking student laboratory Technicians.Students will provide technical assistance concerning experimental preparations and procedures for laboratory classes.Responsibilities include, but are not limited To.Preparing undergraduate laboratory classes, including solutions and

TotalMed Allied is seeking a travel Cath Lab Technologist for a travel job in Hackensack, New Jersey.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: ASAP Duration: 17 weeks 40 hours per week Shift: 8 hours, days Employment Type: Trav

QCi) (Nasdaq: QUBT) is an innovative, integrated photonics company that provides accessible and affordable quantum machines to the world today.QCi products are designed to operate at room temperature and low power at an affordable cost.The Company's portfolio of core technology and products offer un

PRIDE Health is seeking a travel Cath Lab Technologist for a travel job in Rochester, New York.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 09/15/2025 Duration: 17 weeks 40 hours per week Shift: 10 hours, days Employment Type: Tra

I am interested in laboratory operations and analytical methods.

EvolutionaryScale's mission is to develop artificial intelligence to understand biology for the benefit of human health and society, through open, safe, and responsible research, and in partnership with the scientific community.Over the next ten years AI will transform biological design, making mole

Conduct raw material testing and chemical analysis using wet chemistry techniques. Utilize analytical instrumentation such as GC-MS for testing. Experience with analytical instrumentation including GC-MS.

Note: We have a preference for candidates that are able to work out of NYC or SF for this role!.Patronus AI's mission is to provide the security and risk management layer for AI.We are solving the problem of scalable oversight - how can humans continue to supervise AI systems when AI far outperforms

The main function of a lab technician is to manage the prototype device farm to ensure they are ready to perform automated firmware and software tests.A typical lab technician may work under the supervision of a production engineer or a lab manager.This position requires physical presence at Meta's

Anthropic's mission is to create reliable, interpretable, and steerable AI systems.We want AI to be safe and beneficial for our users and for society as a whole.Our team is a quickly growing group of committed researchers, engineers, policy experts, and business leaders working together to build ben

To find out more about EMSL Analytical, Inc.

Pluralis Research is pioneering Protocol Learninga fully decentralised way to train and deploy AI models that opens this layer to individuals rather than well resourced corporates.By pooling compute from many participants, incentivising their efforts, and preventing any single party from controlling

Max Bill Rate: $65/hour Onsite Position- Englewood Cliffs , NJ Duration: 6 months North America Foods Lab Technician Description: This is a temporary role to support laboratory, pilot plant, and analytical work for innovations, renovations, and operations projects within the Condiments and Savory po

This is the main job post content.It focuses on the key details of the job opportunity, including responsibilities, requirements, and other important information.The content is presented in a clear and concise manner, ensuring that all necessary details are included without any unnecessary clutter.T

Medical Laboratory Technician to work in the Core Laboratory under the direct supervision of supervisor and or Medical Laboratory Technologist on duty.Will be responsible for performing a variety of complex and routine test within the Core Laboratory complying with all safety and regulatory requirem

Interact with various software and business groups to develop an understanding of their business requirements and operational processes.Utilize acquired knowledge and business judgment to build decision-supporting and operational tools to improve the bottom line.Build quantitative mathematical model

Performs highly-skilled laboratory functions and other technical duties in support of coursework.Sets up, maintains, and organizes student laboratories.Assists students with setting up experiments and other learning exercises, and with the use of equipment and materials.Maintains appropriate safety

The NYC Department of Environmental Protection (DEP) protects public health and the environment by supplying clean drinking water, collecting and treating wastewater, and reducing air, noise, and hazardous materials pollution.DEP is the largest combined municipal water and wastewater utility in the

Laboratory Technician - Engineering.Faculty is eligible for Tenure Track?.Functions and Responsibilities.Under the supervision of the Chairperson of Mathematics, Engineering Technologies and Computer Sciences Division or designee, the Laboratory Technician is responsible for the maintenance, prepara

Specific tasks for the Analyst may involve: - Provide analytical and technical assistance to brief the Chief and their staff on a daily basis - Prepare documentation for the weekly QoLStat meetings - Prepare and deliver informative, well-organized presentations.

Job DescriptionJob Description .With 19 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies.ERG has 340+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep d

Tandem is a generational opportunity to rethink how we bring new therapies to market, and our path to doing so is significantly de-risked we have:.Exponential organic growth: We have product-market fit and are growing rapidly through word-of-mouth.Tandem supports thousands of patients every day, is

Performs highly-skilled laboratory functions and other technical duties in support of coursework.Sets up, maintains, and organizes student laboratories.Assists students with setting up experiments and other learning exercises, and with the use of equipment and materials.Maintains appropriate safety

Pluralis Research is pioneering Protocol Learninga fully decentralized way to train and deploy AI models that opens this layer to individuals rather than well-resourced corporates.By pooling compute from many participants, incentivizing their efforts, and preventing any single party from controlling

Provides technology and learning support in one or more library facilities.Assists faculty and students in using course-related technologies.Assists students with common technology problems.Provides technical support for library faculty offering instruction and/or workshops, for multi-media resource

Research Scientist - CTRL Labs.Reality Labs at Meta is seeking Research Scientists with experience in product-focused machine learning and signal processing research to advance our pioneering work in neuromotor interfaces, which has grown out of the acquisition of CTRL-labs.We're building a practica

David creates tools to increase muscle and decrease fat.Our first product is a protein bar.More broadly, David is a platform to develop high-protein, low-calorie, blood-sugar-friendly foods that are craveable.This is a compelling opportunity to be a part of an exciting new food brand as we operate w

Receive, label and analyze samples (blood, toxic, tissue etc.Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organi

Artificial Intelligence could be one of humanity's most useful inventions.At Google DeepMind, we're a team of scientists, engineers, machine learning experts and more, working together to advance the state of the art in artificial intelligence.We use our technologies for widespread public benefit an

Receive, label and analyze samples (blood, toxic, tissue etc.Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organi

Research Scientist Intern, Optimization, Privacy and Inference (PhD).Central Applied Science is a research and development team, working to improve Meta's products and infrastructure.We generate real-world impact through a combination of scientific rigor and methodological innovation.Our focus is on

Receive, label and analyze samples (blood, toxic, tissue etc.Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organi

We value solid expertise in Deep Learning with hands-on implementation experience, strong analytical thinking, a deep desire to learn and high motivation. Curious, hardworking and detail-oriented, and motivated by complex analytical problems.

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : New York, NY.Travel Assignment Salary $2452/Week.Travel Allied Job Assignment Length

This is the main job post content.We have removed all extraneous metadata, links, buttons, and other unnecessary elements to focus on the core job post details.The formatting has been adjusted to ensure consistency across our platform.

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Hackensack, NJ.Travel Assignment Salary $2954/Week.Start Date : September 15, 2025.T

Jump Trading Group is committed to world class research.We empower exceptional talents in Mathematics, Physics, and Computer Science to seek scientific boundaries, push through them, and apply cutting edge research to global financial markets.Constant innovation requires fearlessness, creativity, in

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Hackensack, NJ.Travel Assignment Salary $2954/Week.Start Date : September 15, 2025.T

A PhD degree in molecular or cell biology, neurobiology, biochemistry, biomedical engineering, computational biology or other relevant fields. Two years of experience in molecular biology, biochemistry, next generation sequencing methods.

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Hackensack, NJ.Travel Assignment Salary $2614/Week.Start Date : September 15, 2025.T

Experience in biochemistry and molecular biology.

Receive, label and analyze samples (blood, toxic, tissue etc.Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organi

Performs analytical studies to analyze and evaluate data generated under the technology support contract to determine correlations with policy and other legal considerations.

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Hackensack, NJ.Travel Assignment Salary $2934/Week.Start Date : September 15, 2025.T

AI Research Scientist, CoreML - Monetization AI.We are the Monetization Ranking AI Research organization, dedicated to delivering personalized ads that maximize both user utility and advertiser value.We focus on advancing AI and ML technologies for all aspects of Monetization, including ranking, ret

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Englewood, NJ.Travel Assignment Salary $2934/Week.Start Date : September 22, 2025.Tr

Job Opportunity At Synergisticit.Synergisticit wants every candidate to know that the job market is challenging and to stand out, you need to have exceptional skills and technologies and that's where we come in to make sure you get the attention which you need.Position open for all visas and US citi

Host Healthcare is seeking a local contract Cath Lab Technologist for a local contract job in New York, New York.Job Description & Requirements.Host Healthcare Job ID #La1fVJ000006iuKnYAI.Pay package is based on 8 hour shifts and 38 hours per week (subject to confirmation) with tax-free stipend amou

Candidate should excel at clearly articulating analytical findings and offering practical, data-driven solutions.

Host Healthcare is seeking a travel Cath Lab Technologist for a travel job in New York, New York.Job Description & Requirements.Host Healthcare Job ID #a1fVJ000006iuKnYAI.Pay package is based on 8 hour shifts and 38 hours per week (subject to confirmation) with tax-free stipend amount to be determin

This organization is looking to add a permanent and full-time Medical Technologist/Medical Laboratory Technician to their team on either day, evening, or night shift! They also have department specific openings in blood bank, microbiology, core laboratory or special chemistry!.

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : HACKENSACK, NJ.Travel Assignment Salary $2561/Week.Travel Allied Job Assignment Leng

Our Authentication Centers (warehouses) are where the magic happens! The Art & Science of Real comes to life within our facilities located in New Jersey and Arizona combining the knowledge of hundreds of luxury experts with cutting-edge, proprietary technology.As consigned goods travel into our fac

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : New York, NY.Travel Assignment Salary $2452/Week.Travel Allied Job Assignment Length

Research Engineer, Frontier Red Team (Rsp Evaluations).San Francisco, CA | Seattle, WA.Research Scientist, Frontier Red Team (Autonomy).Remote-Friendly (Travel-Required) | San Francisco, CA | Seattle, WA | New York City, NY.Research Scientist, Frontier Red Team (Cbrn, Biosecurity).Anthropic Ai Safet

Receive, label and analyze samples (blood, toxic, tissue etc.Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organi

Our mission is to make healthcare reimbursement transparent and fair, so providers can spend more time caring for patients and less time haggling over costs.We specifically focus on the most complex AI challenges that require novel R&D, with a team that blends AI researchers and engineers with clini

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : HACKENSACK, NJ.Travel Assignment Salary $2561/Week.Travel Allied Job Assignment Leng

Research Engineer, Frontier Red Team (Rsp Evaluations).San Francisco, CA | Seattle, WA.Research Scientist, Frontier Red Team (Autonomy).Remote-Friendly (Travel-Required) | San Francisco, CA | Seattle, WA | New York City, NY.Research Scientist, Frontier Red Team (Cbrn, Biosecurity).Anthropic Ai Safet

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Hackensack, NJ.Travel Assignment Salary $2934/Week.Start Date : September 15, 2025.T

The Center for Health Equity and Community Wellness (CHECW) seeks to eliminate racial and other inequities resulting in premature mortality.With an unwavering grounding in history and structural analysis, CHECW works to increase visibility of the harm perpetuated by centuries of racist, socially unj

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Englewood, NJ.Travel Assignment Salary $2934/Week.Start Date : September 22, 2025.Tr

Processing Technician - Automated Lab/Central Processing Unit - Nights.Step into NewYork-Presbyterian/Columbia University Medical Center, where clinical laboratory professionals are redefining the limits of science and medicine.With patients from across the globe, we study some of the most complex a

TotalMed Allied is seeking a travel Cath Lab Technologist for a travel job in Hackensack, New Jersey.Job Description & Requirements.We are seeking a Technician-Cath Lab Tech for a travel assignment in Hackensack New Jersey.Totalmed allied Job ID #1917148.Pay package is based on 8 hour shifts and 40

Schedule: 3x8-Hour 23:00 - 07:30.Skills: ABO/Rh/Antibody Screen & ID, AHG Crossmatch, Antibody Typing: Tube Method, Antigen Typing, Blood Banking Procedures, Blood Irradiation, Cold Agglutinins, Cord Blood Evaluation, Crossmatch-Immediate Spin/IgG, Direct Coombs (DAT), Electronic Crossmatch, Indirec

With Wanderly you can chat and apply to any agency with Wanderly’s Universal Application, below are the details of this.Specialty: Cath Lab Tech Allied.Travel Catherization Lab Technician (Cath Lab Tech) Allied : Hackensack, NJ.Travel Assignment Salary $2614/Week.Start Date : September 15, 2025.T

Research Engineer, Frontier Red Team (Rsp Evaluations).San Francisco, CA | Seattle, WA.Research Scientist, Frontier Red Team (Autonomy).Remote-Friendly (Travel-Required) | San Francisco, CA | Seattle, WA | New York City, NY.Research Scientist, Frontier Red Team (Cbrn, Biosecurity).Anthropic Ai Safet

Receive, label and analyze samples (blood, toxic, tissue etc.Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organi

Research Scientist, AI (Biology Focus).EvolutionaryScale's mission is to develop artificial intelligence to understand biology for the benefit of human health and society, through open, safe, and responsible research, and in partnership with the scientific community.Over the next ten years AI will t

Receive, label and analyze samples (blood, toxic, tissue etc.Design and execute laboratory testing according standard procedures, make observations and interpret findings Conduct experiments under defined conditions to verify/reject various types of hypotheses using refined scientific methods Organi

The mission of the New York City Police Department is to enhance the quality of life in New York City by working in partnership with the community to enforce the law, preserve peace, protect the people, reduce fear, and maintain order.The NYPD strives to foster a safe and fair city by incorporating

Research Scientist Intern, Graph Science and Statistics Research (PhD).Central Applied Science (CAS) is a research and development team, working to improve Meta's products, infrastructure, and processes.We generate real-world impact through a combination of scientific rigor and methodological innova

Research Scientist - Neuromotor Interfaces.Meta is seeking Research Scientists with experience in product-focused signal processing and machine learning to help us create novel wearable sensors and algorithms to power the next generation of neuromotor interfaces and augmented reality systems.Help us

Design, develop, and fine-tune AI models and analytical frameworks tailored to detect emerging challenges and operational inefficiencies. Excellent analytical, problem-solving, and communication skills, with the capability to simplify complex ideas for diverse audiences.

GLGers also have access to benefits such as:.Comprehensive medical, dental and vision coverage effective on your first day of employment.No pre-determined limits on vacation time, plus 10 company holidays.Roth 401(k) plans with an employer match (subject to annual limits & vesting).Tuition reimburse

Success in this role requires analytical experience across healthcare markets, federal and state policies, and reimbursement structures.

A minimum of 2+ years of experience in a banking, research role, or accounting focused role which may include working as a desk analyst, investment banking analyst, or other analytical and demanding roles. We are seeking a credit trained, highly analytical, creative, and self-motivated individual to

Our New Associate Program is a full-time program for individuals who have 2-5 years of experience and an advanced degree.As a new associate, you will be an integral part of our business and develop product-specific and function-specific skills and interact closely with senior professionals and clien

Pharmaceuticals & Biotechnology Equity Research Analyst.The Pharmaceuticals & Biotechnology Equity Research team covers both large and small biopharmaceutical companies that develop and sell products in almost all disease areas, both US and internationally.The lead analyst is top three ranked in the

Associate, Prospect Research & Outreach.Part-Time Prospect Research and Outreach Associate.DonorsChoose makes it easy for anyone to help a teacher in need, moving us closer to a nation where students in every community have the tools and experiences they need for a great education.Since 2000, more t

Credit Derivative And Index Research Associate.One of the world's most highly respected advisory franchises, J.Morgan's fundamental and quantitative research has earned top rankings in surveys by Institutional Investor.We provide thoughtful and differentiated analysis on sectors and companies, actio

Requires expert level analytical and quantitative skills with proven experience in developing strategic solutions for a growing matrix-based multi-industry sales environment.

At Piper Sandler, we connect capital with opportunity to build a better future.We believe that diverse teams with unique backgrounds, skills and experiences yield more innovative solutions.This is reflected in our commitment to engage, hire, and retain bright, committed people to work in partnership

Strong analytical and sales skills.

Jefferies is seeking an equity research associate to support the TMT Research Group covering Technology and Internet.The candidate will support the TMT research team in delivering extensive company and industry research, constructing detailed financial/valuation models, and marketing written researc

Research, Equity Research Associate, Utilities & Power.The Associate will be responsible for assisting a Senior Analyst in the Healthcare sector focusing on Utilities & Power.The main focus of this role will be conducting primary research, including financial analysis, due diligence on industry tren

Strong analytical and sales skills.

Publish proprietary equity research in industries aligned to the firm's banking sectors exhibiting the firm's expertise in the sector.Create and publish proprietary equity research content in designated industry with stock recommendations (Buy, Hold, Sell) to institutional buy-side clients.Conduct d