Chemist Jobs in Morris, NJ

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

Role: Tech BA - Trade Analytics Duration: Fulltime Inputs to look for matching profiles - Trade Analytics Tech BA with experience in Trade Analytics (exposure, routing to brokers with low trade cost and high execution, ADR vs stock routing for hedging, generate alpha etc Job Description: BA/BS Degree in finance, computer science or related field 8+ years of relevant Asset Management experience working as an IT business systems analyst or individuals with business analyst experience looking to transition to technology. 5-7+ years of experience in systems development life cycle including the ability to define and document specifications, work with developers to design/analyze alternative technical solutions, test completed code and complete a smooth implementation with the business partners. 5-7+ years of experience conducting requirements-gathering meetings with users, developers, system design architects, system integrators and vendors. 5+ years of experience working in a cross functional environment while supporting multiple lines of stakeholders, such as trading, portfolio management, compliance, and/or risk. 5+ years of experience partnering with Agile team members to generate requirement stories, UAT test scripts, release notes, and other project artifacts. 5+ years of experience analyzing and providing technology recommendations to the business. 3-5+ years of working knowledge in Visio, Lucid Chart or other visualization software, with experience building flowcharts to represent workflows. 3-5+ years of experience with collaborative tools such as Jira, Azure DevOps (ADO) and Confluence. Coordinating user acceptance testing between vendor, business and NTAM technology team. 8+ years' experience as business analyst or product member in Investments Asset Management (front office), preferably Trading. Experience in Order management system, Aladdin OMS, or Charles River focused on Portfolio Management and/or Trading. Lead teams thru requirements, story writing and sprint planning Experience with directly working with Portfolio Managers or Traders in Investments, enhancing workflows and user experience. Preferred Qualifications: Finance CFA Foundation or CFA certification. Subject matter expertise and experience with OMS/EMS, Order Management Systems - BlackRock Aladdin, CRD or other widely used enterprise OMS solutions. EMS solutions - Virtu Triton, Bloomberg EMSX. Extensive experience in the financial Asset management, particularly equity trading, portfolio management, operations, and accounting. Experience in component-based development (integrating vendor products with in-house developed code). Strong data analysis skills and working experience in an agile development environment. Confidence in presenting both strategic and tactical vision to the business team for both big-picture planning and day-to-day management of project goal. Desire to work with both in-house developed systems and third-party vendor packages. Excellent communication, interpersonal, analytical, problem solving, organizational and negotiation skills. Ensuring that system solutions are delivered successfully to the business stakeholders. Providing deep data support and maintenance of vendor applications and in-house systems, as needed. Gaining in-depth business knowledge to successfully represent the business community in arriving at technical solutions that support business strategies. Adapting to changing priorities and managing multiple tasks.

DUTIES & RESPONSIBILITIES: Essential Duties and Responsibilities include, but are not limited to, the following: • Independently perform analytical testing including but not limited to FTIR and Raman spectroscopy methods, color & physical appearance tests, pH and osmolality measurements, compendial wet chemistry identification methods (e.g., USP), and other general analytical lab techniques. Executed tests will support clinical release and stability testing of drug substances, drug products, excipients and raw materials used in the manufacturing and formulation of Clinical drug substances and drug products. • Demonstrate practical knowledge of analytical techniques contributing to the development of phase-appropriate robust and reproducible analytical methods used in a GMP testing laboratory. • Maintain clear, complete, accurate and GMP-compliant documentation for experiments. • Independently execute analytical method qualifications, verifications, and validations (as applicable), carefully adhering to approved protocols. • Contribute to study design and the authoring of analytical protocols and reports. • Proactively provide clear, timely communication of potential issues to management. • Organize and present data for internal meetings. • Proactively provide clear, timely communication of potential issues to management. Professional Qualifications: • The candidate must have a B.S. or equivalent with a degree in Analytical Chemistry, Chemistry, Biochemistry or equivalent; 1-2 years of analytical laboratory experience in a GMP environment is strongly preferred. • An understanding of cGMP/GLP and GDPs practices and EHS requirements is essential for success in this position. Ability to comply with all applicable SOPs, internal and external (ICH, compendial) requirements/regulations is a must. • The candidate must be able to deliver when working under assigned timelines and demonstrate good communication skills, particularly in documentation of data and writing reports and methods. Skill in communicating/escalating critical issues to appropriate team leaders and functional area management is necessary. • Expertise in MS Office applications, in particular MS Word and Excel, is required. Familiarity with electronic documentation systems (e.g., Qumas, Infinity, Syncade-DCA) for routing protocols/reports, investigation reports for review and approval is a plus. • Experience in use of scientific reporting applications and ELN software, e.g., VelQuest, Symyx and LIMS is preferred.

* Work independently and/or cross-functionally to initiate and execute lab works on evaluation of recyclability, pulpability, and biodegradation of various materials. * Responsible for collecting and recording, interpreting and documenting data in a manner consistent with Good Documentation Practices * Abe to be aware and comply of all relevant standard Operating Procedures (SOPs) * Manages and prioritizes assigned projects with little or no direction. Quals-- Must be reliable/dependable Good technical skills with training in wet chemistry laboratory safety is a must. Comfort and knowledge of working with chemicals, especially hazardous chemicals. Ability to perform heavy lifting (5 lb. up to 40 lb.). Organized with good time management skills. Good communications and observation skills Good focus and attention to detail. Ability to travel and work with outside agencies (Somerset Raritan Valley Sewerage Authority). Ability to perform repetitive work on a weekly basis. Appreciation of good housekeeping and ability to clean glassware thoroughly and repetitively. willing to conduct tedious/repetitive work. Degree requirement, BS in Chemistry, Chemical Engineering, Biology, Biological Engineering, Microbiology, Packaging, Materials Science or Polymer Science would be preferred, However we are also open to candidates with high school/community college background as long as this person is dedicated and has a can-do attitude.

SGS is the global leader and innovator in inspection, verification, testing and certification services. Founded in 1878, SGS is recognized as the global benchmark in quality and integrity. With over 97,000 employees in 130 countries and operating a network of more than 2,400 offices and laboratories, we provide services to almost every industry by assuring quality and safety of products and services. Trusted all over the world, SGS is a market leader because we put 100% passion, pride and innovation into everything we do. We encourage new ideas. We welcome people who challenge the way we do things. And we will be 100% committed to helping you reach your full potential. Summary As the Laboratory Technician, you will perform performance, chemical, and physical testing of samples such as fabrics, garments, accessories, and other soft goods among others to determine performance properties as well as other characteristics. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Job Functions Perform routine laboratory testing, following the relevant company's Standard Operating Procedures (SOP's) and methods. Validate performance on methods as required. Test to applicable standards (ASTM, CSPA, ISO, SSC, etc.) and customer-specific protocols. Determines the type of testing based on the appropriate guidelines and regulations. Accurately complete and maintain all laboratory reports. Responsible for sample breakdown and preparation, including extraction of materials from finished products as required for testing. May be required to receive, sort, log client samples into the database, and prepare sample labels. Perform daily, weekly, and monthly Quality Assurance/Quality Control checks on equipment. Assist in keeping inventory of laboratory chemicals and equipment necessary for the day-to-day functioning of the laboratory and in compiling a list of supplies to be ordered when needed. Assists in calibration/verification tasks and other ISO 17025 related activities. Ensure all personal protective equipment (PPE) relevant for tasks is worn at all times. Adheres to internal standards, policies, and procedures. Performs other duties as assigned. Summary As the Laboratory Technician, you will perform performance, chemical, and physical testing of samples such as fabrics, garments, accessories, and other soft goods among others to determine performance properties as well as other characteristics. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Job Functions Perform routine laboratory testing, following the relevant company's Standard Operating Procedures (SOP's) and methods. Validate performance on methods as required. Test to applicable standards (ASTM, CSPA, ISO, SSC, etc.) and customer-specific protocols. Determines the type of testing based on the appropriate guidelines and regulations. Accurately complete and maintain all laboratory reports. Responsible for sample breakdown and preparation, including extraction of materials from finished products as required for testing. May be required to receive, sort, log client samples into the database, and prepare sample labels. Perform daily, weekly, and monthly Quality Assurance/Quality Control checks on equipment. Assist in keeping inventory of laboratory chemicals and equipment necessary for the day-to-day functioning of the laboratory and in compiling a list of supplies to be ordered when needed. Assists in calibration/verification tasks and other ISO 17025 related activities. Ensure all personal protective equipment (PPE) relevant for tasks is worn at all times. Adheres to internal standards, policies, and procedures. Performs other duties as assigned. Qualifications Education and Experience Required: High School diploma or GED Preferred: Degree in Textiles or related science Associates degree in a related scientific field 3+ years working in a lab setting with experience following strict safety standards, or equivalent education and experience Pay: $21.15 - $26.44/ hour Additional Information Benefits Competitive salary. Comprehensive health, dental, and vision insurance for full time employees. Retirement savings plan. Continuous professional development and training opportunities. A dynamic, collaborative work environment. Access to cutting-edge cryptographic technology and tools. Physical Demands of the Job Stand: Occasionally Move or traverse: Frequently Sit: Constantly Use hands: Constantly Reach with hands and arms: Occasionally Climb or balance: Occasionally Stoop, kneel, crouch or crawl: Occasionally Talk/hear: Constantly Taste/Smell: Occasionally Lift/carry/push or pull: Occasionally 30 lbs Additional information SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time. If you are applying for a position within the United States and you have difficulty completing the on-line employment application because of a disability, please call ************ for assistance and leave a message. You will receive a callback. Please note, this phone number is not for general employment information but is only for individuals who are experiencing difficulty applying for a position due to a disability.

QC Analytical Associate II - Allendale, NJ Our vision is creating future cell therapy miracles together. We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies, and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company. The Quality Control Analytical Associate II serves as a supporting role to clinical and commercial production. The QC Analytical Associate II will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. Essential Functions and Responsibilities Performs the accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or efficacy of different cell populations Performs maintenance, monitoring, and troubleshooting of pertinent equipment Performs and assists in the training of other Quality Control technicians Maintains training records and coordinates records retention with Document Control and Training groups Tests, documents, and reports results for products or materials following company and/or client procedures following CGMP and/or GTP guidelines Performs state proficiency testing and/or client proficiency testing under direct supervision as applicable Participates in managing QC materials and supplies Performs and assists in equipment and method qualification/validation activities as needed Performs reagent and media preparation Provides input based on level of knowledge and experience with troubleshooting malfunctioning equipment Investigates out-of-specification, out-of-trend, aberrant, and/or non-conforming test results Initiates, investigates, and prepares deviation reports with input from assigned supervisor Brainstorms and implements corrective and preventive actions, as and when applicable Documents training and execution of shipping test samples to contract laboratories for testing Completes all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) Communicates effectively with other co-workers, departments, management and clients Eventually serves as a lead and/or co-lead for client projects Additional tasks as assigned Qualifications and Competencies: BA/BS in a science or relevant field required Experience in GMP, cell count, flow cytometry, documentations, flexibility, CBC, ELISA, qPCR Prior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a cGMP/GTP environment preferred Prior industrial experience in cell count methodologies preferred Prior academic and/or industrial cell therapeutics experience preferred Minimum 2-4 years of experience in QC lab setting or withing biopharma industry

Required Skills & Experience • Familiarity with common chemicals/solvent property databases, laboratory practices/equipment and general lab safety practices • Experience working in a GMP-regulated environment and ability to follow established procedures required to comply with safety • Experience working with or troubleshooting lab equipment and/or electronics • Domestic and International compound shipment experience/trade compliance experience • Experience working in Ariba Job Description Insight Global is seeking a Prep Lab Technician to join the Chemical Engineering Research and Development department of a pharmaceutical client located in Rahway, New Jersey/ This employee will support laboratory scientists through centralizing a variety of tasks needed to maintain the laboratories in good working order. The role will be responsible for domestic and international shipments, checking eye-wash stations in laboratories, and monthly weight checks of GMP balances and scales, in addition to other work.

Opportunity Description Main purpose is to assist in all tasks associated with the Analytical Laboratory (Quality Control, Analytical R&D). Company Information Biopharma Performing analytical laboratory testing in a cGMP environment Preparing solutions and reagents for experimentation as required Follow instructions from immediate supervisor for day to day activates/schedule Perform quantitative and/or qualitative analyses on samples Follow written Standard Operating Procedures (SOPs), monographs and methods Use various analytical equipment (HPLC, Dissolution Apparatus, Karl Fisher, Laser Diffraction PSD, Aerodynamic PSD) Document methods and results into laboratory notebooks and logbooks Follow safe laboratory practices Maintain Chemical reagents and supplies for analytical chemistry work Education Bachelor's in chemistry or related field Experience & Skills Required (Entry Level, 1-3 years in a pharmaceutical laboratory preferred)

QC Analytical Associate I - Allendale, NJ Our vision is creating future cell therapy miracles together. We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies, and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company. The Quality Control Analytical Associate serves as a supporting role to clinical and commercial production. The QC Analytical Associate will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. Essential Functions and Responsibilities: Performs the accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or efficacy of different cell populations Performs maintenance, monitoring, and troubleshooting of pertinent equipment Tests, documents, and reports results for products or materials following company and/or client procedures following CGMP and/or GTP guidelines Performs state proficiency testing and/or client proficiency testing under direct supervision as applicable Participates in managing QC materials and supplies Performs and assists in equipment and method qualification/validation activities as needed Performs reagent and media preparation Provides input based on level of knowledge and experience with troubleshooting malfunctioning equipment Investigates out-of-specification, out-of-trend, aberrant, and/or non-conforming test results Initiates, investigates, and prepares deviation reports with input from assigned supervisor Brainstorms and implements corrective and preventive actions, as and when applicable Documents training and execution of shipping test samples and equipment to contract laboratories for testing Completes all documentation according to written Standard Operating Procedures in accordance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Communicates effectively with other co-workers, departments, management and clients. Additional tasks as assigned. Qualifications and competencies: BA/BS in a science or related field required Prior cGMP experience preferred Basic lab equipment experience, cell count, flow cytometry, CBC, documentation Prior academic and/or industrial cel therapeutic experience preferred Minimum 0-2 years of experience in QC Lab setting or withing the biopharma industry Candidate must be detail oriented, can multi-task, work in a team environment, and have the flexibility to adapt to company growth as well as its evolving responsibilities

Part of kdc/one, Zobele is a multinational, global leader in product development and manufacturing, key partner of the top Home & Personal Care FMCG´s companies. To meet our growth challenges we're looking for proactive, enthusiastic and talented professionals willing to join our team. For our North America Business Development Centre in Somerville (New Jersey), we are currently looking for a: LABORATORY & PRODUCT DEVELOPMENT TECHNICIAN Our Laboratory & Product Development Technician manages the activities of laboratory (testing, results reporting, certificates of analysis, tools, samples archive) and organizes the activities to support all the product development phase Scouts and proposes innovative materials and formulation performing evaluation and validation protocols for the realization of specific products/technologies. Responsibilities: Timely executes and record all the laboratory tests, according to Divisional plans and needs, releasing the products if applicable. Is responsible for the correct maintenance and functioning of the laboratory tools, equipment, and infrastructures, taking care of calibration, and repairing activities and contributing to new instruments selection and calibration methods issue. Manages the retained samples archive, ensuring clear samples identification and tidy storage. Collaborate to the study, issue and update of the innovative technologies and Product, constantly monitoring the relative normative evolution. Identify and manage contacts with external technology sources (suppliers, laboratories, institutes, consultants…). Requirements: Fluent English University degree, preferably in technical fields (chemistry for chemical labs as requirement) 1+ year of experience in laboratories, Chemical formulations 2+ years in Product Innovation (Formulations and Processes) in FMCG industry. (Laundry Care, Toilet Care, Home Cleaning). Test methods and relative normative Laboratory instruments Metrology IT tools (MS Office, SAP R/3 QM module as preferable) Global mind-set, commercial understanding of corporate and operational business issues. Excellent problem resolution and technical decision-making abilities. Well organized, dynamic, and able to multitask and change focus quickly when required. Organizational skills Precision Join US! Apply now and join the kdc/one worldwide team! Zobele by kdc/one is an Equal Opportunity Employer and as such, treats all applications equally and recruits purely on the basis of skills and qualifications.

TotalMed Allied is seeking a travel Cath Lab Technologist for a travel job in Morristown, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel We are seeking a Technician-Cath Lab Tech for a travel assignment in Morristown New Jersey. Totalmed allied Job ID #1722372. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Technician-Morristown in New Jersey About TotalMed Allied In the fast-paced, highly competitive industry that is healthcare, you need a partner who works for and with you. At TotalMed, we're a team who really cares. Our goal is to give gold standard customer care by enhancing the recruiter - traveler partnership with a high level of integrity and fun while supporting the experience you want to have throughout your travel career. Our recruiters can help you evaluate the best healthcare jobs offered nationwide by uncovering your ideal career path and providing as much information as possible to assist in making the best decision for you in a no pressure atmosphere. We care like no other so that you can care like no other. What the TotalMed experience can offer you: Top paying contracts 24x7 concierge one-on-one service to meet your needs Long or short term contracts available nationwide Top 10 agency per recent traveler surveys - Highway Hypodermics - Travel Nursing Central Come experience the “Care like no other” difference!

Hello we are looking for a Lab Technician II in Edison, NJ! in Edison, NJ. Key Details: Shift: 7:30 AM to 4:00 PM Location: Edison, NJ 08817 Top 3 Must-Have Skills: Basic lab instrumentation knowledge Ability to follow lab procedures Strong data entry and reporting skills Key Responsibilities: Perform polymerizations and physical testing of polymers. Maintain lab procedures, ensure quality compliance, and troubleshoot quality issues. Operate efficiently to prevent resource waste. Manage safety and environmental responsibilities, including ISO instrument calibrations. Handle tasks requiring physical activity, such as loading/unloading materials. Requirements: High School Graduate: 5+ years of laboratory experience. Associate Degree: 2+ years of lab experience. BS in Chemistry (or related field): No experience required.

Essential Functions and Responsibilities Ensure all procedures and processes comply with internal quality standards and external regulations for pre-clinical, clinical, and commercial manufacturing. Read, comprehend, and adhere to cGMP and cGTP documentation for Quality System Functions (SOPs, WIs, etc.). Maintain cGMP and cGTP compliance in all areas of pre-clinical, clinical, and commercial manufacturing. Release raw materials in the ERP system and record manually. Perform accessioning of incoming apheresis. Review batch records and manage material disposition for finished products to clients. Provide information regarding Out of Specification results and deviations to investigators. Conduct line clearance before the start of manufacturing operations. Support tech transfer activities. Perform additional duties as assigned. Qualifications Bachelor's degree or higher in a scientific field. 0-2 years of experience in a biologics or biotechnology company. Familiarity with the aseptic manufacturing process for biologics is preferred. Knowledge of GMP and TCTP regulations. Experience reviewing GMP/GCTP-related documents (validation/qualification reports, SOPs, etc.). Competencies/Candidate Profile Proficient in relevant computer software (Microsoft Office, Outlook). Strong attention to detail and organizational skills. Excellent analytical and problem-solving abilities. Effective written and oral communication skills. Capable of multi-tasking and adapting to change. Flexible and able to adjust to the company's growth and evolving responsibilities. Able to work both independently and as part of a team.

Nightingale Nurses is seeking a travel Cath Lab Technologist for a travel job in Somerville, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel About Nightingale Nurses the first name in travel nursing You may not realize it, but as an RN with real world hospital experience, you are legendary. To the lives you've helped save, the patients you've cared for, and to the hospitals where you've done it. And you're just getting started. Legendary is where Nightingale begins. We're the first name in travel nursing, representing only the very best RNs. That's why hospitals prefer us, allowing us to offer exceptional travel nursing assignments all over the US, as well as the highest pay rates and most extensive benefits in the industry. Nightingale facilitates every aspect of your travel nursing assignment, so you can focus on doing what you do best. We want you to grow, explore, and enjoy unrivaled liberty, the freedom to nurse.

Epic Travel Staffing is hiring a Travel - Cath Lab Tech Shift: Days / 8a-6:30p, 10x4, 40 hours per week, Monday-Friday Length: 13 weeks Requirements: NJ License 2-3 years of current cath lab (CV) experience Must have Cardiac Cath Lab and Vascular Experience Must have experience with PPM Implants and Vascular procedures Experience with the following equipment: IVUS, PFR, IFR... Experience with scrubbing in procedures for cardiac cath and vascular invasive procedures using a Philips x-ray machine Must have Scrubbing, circulating and monitoring experience, knowledge of procedures, 2HC/RHC/PCI, Peripheral Angiogram, PTA, PPM Implant BLS ARRT(R) RCIS ACLS preferred Neuro experience preferred Charting: GE Mac Lab and Cerner preferred Other Details: 1st time travelers accepted Locals Accepted Local Radius: 50 miles Shift: 8a-630p...ARRT(R) (NJ License required), or RCIS...BLS required…ACLS preferred…2-3 years of current Cath Lab (CV) experience required…Neuro experience preferred...Must have Cardiac Cath Lab and Vascular Experience…Must have experience with PPM Implants and Vascular procedures…No blocked scheduling…Call Required: Minimum of at least 7 days of call during the month, including weekends & holidays Charting: GE Mac Lab and Cerner - preferred…Types of procedures: cardiac cath, PCI, Fistogram, Vascular Angiogram, PTA, PPM Implant…Experience with the following equipment: IVUS, PFR, IFR...Experience with scrubbing in procedures for cardiac cath and vascular invasive procedures using a Philips x-ray machine…Must have scrubbing, circulating and monitoring experience, knowledge of procedures, 2HC/RHC/PCI, Peripheral Angiogram, PTA, PPM Implant…1st time travelers accepted…Scrubs provided by the hospital - change daily; Can bring own lead aprons but unit will provide as needed… COVID-19 Vaccine (Facility Guideline): Required + Booster - Medical/Religious Exemptions only Flu Vaccine (Facility Guideline):Unknown Unit: Cath Lab, 106426 Epic Travel Staffing: Day 1 health insurance coverage and comprehensive benefits options 401(k) matching program Weekly direct deposit Concierge state licensing program for RN and other healthcare modalities in multiple states, including CA Industry leading allowances and reimbursements Referral program with cash bonuses and additional perks Exclusive job openings - Only at Epic Epic Elite Program - Priority status at top facilities and exclusive loyalty bonuses Epic Staffing Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, housing, age, disability, or genetics. We will consider all qualified applicants for employment, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws. By applying for this position, you agree that any calls from Epic Staffing Group and its subsidiaries may be monitored or recorded for training and quality assurance purposes. Pay rate is estimated based on weekly gross income. Weekly gross pay based on qualifications and experience. Rate applies to travel positions only (50+ miles from permanent address). Estimated Weekly Rate: $2595 per week Job ID: 902354

TotalMed Allied is seeking a travel Cath Lab Technologist for a travel job in Somerville, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel We are seeking a Technician-Cath Lab Tech for a travel assignment in Somerville New Jersey. Totalmed allied Job ID #1724382. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Technician-Somerville in New Jersey About TotalMed Allied In the fast-paced, highly competitive industry that is healthcare, you need a partner who works for and with you. At TotalMed, we're a team who really cares. Our goal is to give gold standard customer care by enhancing the recruiter - traveler partnership with a high level of integrity and fun while supporting the experience you want to have throughout your travel career. Our recruiters can help you evaluate the best healthcare jobs offered nationwide by uncovering your ideal career path and providing as much information as possible to assist in making the best decision for you in a no pressure atmosphere. We care like no other so that you can care like no other. What the TotalMed experience can offer you: Top paying contracts 24x7 concierge one-on-one service to meet your needs Long or short term contracts available nationwide Top 10 agency per recent traveler surveys - Highway Hypodermics - Travel Nursing Central Come experience the “Care like no other” difference!

Nightingale Nurses is seeking a travel Cath Lab Technologist for a travel job in Paterson, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel About Nightingale Nurses the first name in travel nursing You may not realize it, but as an RN with real world hospital experience, you are legendary. To the lives you've helped save, the patients you've cared for, and to the hospitals where you've done it. And you're just getting started. Legendary is where Nightingale begins. We're the first name in travel nursing, representing only the very best RNs. That's why hospitals prefer us, allowing us to offer exceptional travel nursing assignments all over the US, as well as the highest pay rates and most extensive benefits in the industry. Nightingale facilitates every aspect of your travel nursing assignment, so you can focus on doing what you do best. We want you to grow, explore, and enjoy unrivaled liberty, the freedom to nurse.

Epic Travel Staffing is hiring a Travel - Cath Lab Tech Shift: Days, 7a-3:30p, 8x5, 40hrs per week, On-call every third week Length: 13 weeks Requirements: NJ License Minimum 2 years experience Need experienced Cath Lab tech AHA BLS ARRT with corresponding sub certification Epic Travel Staffing: Day 1 health insurance coverage and comprehensive benefits options 401(k) matching program Weekly direct deposit Concierge state licensing program for RN and other healthcare modalities in multiple states, including CA Industry leading allowances and reimbursements Referral program with cash bonuses and additional perks Exclusive job openings - Only at Epic Epic Elite Program - Priority status at top facilities and exclusive loyalty bonuses Epic Staffing Group provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, housing, age, disability, or genetics. We will consider all qualified applicants for employment, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws. By applying for this position, you agree that any calls from Epic Staffing Group and its subsidiaries may be monitored or recorded for training and quality assurance purposes. Pay rate is estimated based on weekly gross income. Weekly gross pay based on qualifications and experience. Rate applies to travel positions only (50+ miles from permanent address). Estimated Weekly Rate: $2864 per week Job ID: 840683

Nightingale Nurses is seeking a travel Cath Lab Technologist for a travel job in Paterson, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel About Nightingale Nurses the first name in travel nursing You may not realize it, but as an RN with real world hospital experience, you are legendary. To the lives you've helped save, the patients you've cared for, and to the hospitals where you've done it. And you're just getting started. Legendary is where Nightingale begins. We're the first name in travel nursing, representing only the very best RNs. That's why hospitals prefer us, allowing us to offer exceptional travel nursing assignments all over the US, as well as the highest pay rates and most extensive benefits in the industry. Nightingale facilitates every aspect of your travel nursing assignment, so you can focus on doing what you do best. We want you to grow, explore, and enjoy unrivaled liberty, the freedom to nurse.