Chemist Jobs in Bayonne, NJ

QC Chemist Job Title: Quality Control Laboratory Chemist - Radiopharmaceuticals Evergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, developing our own radiopharmaceutical products and providing contract development and manufacturing services for other radiopharmaceutical companies. We also operate our own cutting edge cancer research laboratories. Evergreen is a small team, where all team members support each other in a variety of activities. We are looking for team members who are motivated to take on new challenges and excited to help build the company. Job Description: We are seeking a highly skilled and experienced Quality Control Laboratory Chemist to join our team in the Radiopharmaceuticals division. This critical role involves the quality control processes documentation development, analytical methods improvement, and ensuring compliance with regulatory standards. The ideal candidate will have extensive experience in the pharmaceutical or radiopharmaceutical industry, a strong background in analytical chemistry, and well development technical writing capabilities. Key Responsibilities: Develop, optimize, and validate analytical methods for testing radiopharmaceutical products, including HPLC, GC, and TLC techniques. Troubleshoot and resolve issues related to laboratory equipment, ensuring proper functioning and accurate results and offering expertise and executing tasks related to department objectives and quality initiatives. Support the validation of analytical procedures, ensuring they meet internal specifications and regulatory requirements. Write, develop, and analyze methods and protocols for new and existing testing procedures. Serve as a key resource for the team, providing client support and managing communications related to reports, calls, and project updates. Contribute to the development of QC-specific protocols and reports, particularly for analytical method validation and related documentation. Collaborate with cross-functional teams and assist with the execution of client-driven requirements, ensuring that testing processes are aligned with regulatory standards. Lead and support efforts in continuous improvement projects that aim to optimize laboratory processes, increase efficiency, and enhance the overall quality system. Assist with departmental initiatives, including recruitment, training, and development of team members, as well as contributing to team scheduling and resource management. Ensure the accurate documentation of all testing results, protocols, and reports in compliance with GMP, GLP, and other regulatory guidelines. Qualifications: 5+ years of experience in the pharmaceutical, life sciences, or radiopharmaceutical industry Bachelor's degree in a scientific field (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences), or equivalent relevant work experience. Extensive experience with laboratory techniques, including HPLC, GC, and TLC, with a strong ability to troubleshoot and resolve issues related to these methods. Proven ability to develop, modify, and validate analytical methods for a variety of testing procedures. Strong written and verbal communication skills, with experience developing and writing technical reports, protocols, and validation documents. Demonstrated ability to work independently as well as collaborate effectively with cross-functional teams. Experience in supporting client needs, including providing timely updates, addressing inquiries, and delivering high-quality reports. Knowledge of GMP, GLP, and other regulatory requirements for pharmaceutical testing and documentation. Working Environment: Laboratory setting with exposure to radiation and other chemical hazards. Fast-paced laboratory setting with responsibility for multiple concurrent projects and tasks. Opportunity to contribute to team improvement, including process optimization and team development. Collaborative environment with a focus on innovation and continuous growth in the radiopharmaceutical sector.

Job Title: Process Chemist Department: Process R&D Job Type: Full Time Director of Process Chemistry We are seeking a highly motivated and skilled Process Chemist to join our Process R&D Department at Porton J-STAR. In this role, you will be responsible for the development, optimization, and scaling of chemical processes for pharmaceutical production. You will collaborate with cross-functional teams to ensure that our processes are efficient, cost-effective, and compliant with regulatory standards. This job description applies to activities and responsibilities associated with the process chemistry development group and support of GMP Operations. Responsibilities Follow existing synthetic routes, making processing improvements where necessary, while conducting multi-step organic synthesis Plan and organize routine operations to maximize production output. Design novel synthetic routes and carry out multi-step organic synthesis. Operate simple open access HPLC/UV, LC/MS, MS, NMR, GC/MS, and other analytical instruments required to monitor reaction processes. Consult with management, the Analytical Department, the Director of GMP Operations and others on issues concerning experiments prior to and during GMP production. Accurately make and check calculations, prepare raw materials, reagents and solutions in accordance with company SOP's. Faithfully record procedures and results in Batch Records or Solution Preparation Forms, notebooks, or other appropriate forms in an organized manner as dictated by departmental SOP and GMP regulations. Write reports on research as required. Promote compliance with cGMP regulations. Attend GMP training sessions. Support management and maintenance of the SOP and Document Control system. Work with clients to develop material release tests and specifications for materials supplied by J‑STAR. Help ensure that client project needs, requirements, and timelines are communicated to, and coordinated between, GMP Operations and Quality Control. Conduct process chemistry R&D for clients as an individual contributor, which includes, but is not limited to, research on synthetic routes to active pharmaceutical ingredients and chemical intermediates by route discovery, process optimization, safety evaluation, enabling technologies, high throughput screening and chemo/biocatalytic reaction discovery and optimization. This will include R&D under c-GLP and potentially under c-GMP conditions. Develop safe, timely and efficient chemical processes by using established, new and/or novel chemical methodologies and processes. Coordinate analytical chemistry methodology to process and/or catalysis discovery, development optimization and problem solving. Maintain an uncompromising focus on quality, documentation, confidentiality and scientific execution. Participate in idea generation for selective quotes/proposals to clients as well as successfully execute against accepted quotes. Initiate cross-department communication and develop coordinated R&D, processing schedules and deliverables Lead and contribute to scientific and technical discussions with co-workers and clients to plan, execute, resolve issues and problem solve. Communicate candidly, clearly and timely with clients, management and peers. Participate in weekly client updates as needed, prepare weekly reports, contribute to and lead campaign reports and participate in process chemistry technology transfer. Coordinate and author professional campaign reports, research summaries, and tech packages. Follow all company, site and laboratory Environmental, Health and Safety (EHS)-related protocols, processes, guidelines and SOPs. Actively participate in EHS discussions with peers and management for continuous improvement of EHS practices. Maintain a clean and well-organized hood, bench, glove-box and common work area that is free of clutter, excess chemicals/samples. Advocate for these principals and positively influence others in this regard. Qualifications Required MS, PhD degree in Organic Chemistry. Proven track record meeting aggressive targets as related to safe, timely and successful synthetic organic chemistry projects. Knowledge and experience base of working in a c-GMP environment is preferable, but not required Excellent written, verbal and presentation skills. Experience in small molecule drug development is preferable, but not required. Track record of scientific success as measured by publications and presentations. Ability to prioritize and manage numerous activities simultaneously. Ability to interact in an effective and appropriate manner with diverse population sets. Experience in working on and positively contributing to scientific teams. Ability to perform the physical requirements of the position.

Job Details: Chemist Global Pharmaceutical Company Contract, Long Term Will start in Skillman, NJ and move to Summit, NJ in the summer Pay up to $33-34/hr The Scientist, Analytical Advanced Models and Methods is responsible for planning and conducting moderately complex experiments, analyzing results, and providing solutions to problems of moderate complexity. You will also keep accurate records, review case report forms, and present data at in-house meetings: Key Responsibilities Develop advanced analytical models and methods to solve complex scientific problems Utilize innovative techniques to analyze data and generate insights Collaborate with cross-functional teams to design and implement cutting-edge solutions Stay current with industry trends and advancements in analytical methodologies Conduct in-depth research in assigned areas using cutting-edge methodologies Analyze and interpret complex data to provide actionable insights Continuously explore and integrate new technologies to enhance analytical capabilities Present findings and recommendations to stakeholders in a clear and compelling manner Present findings and recommendations to stakeholders in a clear and concise manner Qualifications What we are looking for Required Qualifications Bachelor's Degree in Chemistry, Materials Science or equivalent in a related field 2-4 years of experience in developing analytical models and methods using instrumentation techniques such as SEM, DSC, TGA, HPLC, UPLC, FTIR, LC/MS and GC/MS Proven track record of developing and implementing analytical solutions Strong proficiency in statistical analysis and data visualization tools Ability to think critically and problem-solve creatively Excellent communication skills and ability to work effectively in a team environment Desired Qualifications Experience with chemometrics and statistical tools such as PCA, PCR, and PLS Experience with programming languages such as Python, SAS, MATLAB Strong understanding of statistical methods and machine learning algorithms Experience with formulation chemistry across a wide variety of product types (e.g. emulsions, suspensions, solid oral dosage forms)

Specialty paint, coatings, and additives company is looking for a Coatings Chemist with application development experience. The position is located in Fairfield, NJ Responsibilities: Solve customer problems by applying our additives to the customer coatings problems. The employee is primarily responsible for working in a lab to test and evaluate those solutions Explore R&D teams new additives for potential applications Daily working on the bench Spraying and testing of formulations Extensive tracking of data Work from formulation to plant scale up. Interact with internal and external customers. Requirements The employee must have at least a Bachelor's degree in Chemistry. Masters or PHD is a plus. 5 years Coatings work experience is required Confident working in a lab Strong Application Development skills Strong organization skills are important to effectively manage the wide range of responsibilities. The employee must be able to clearly and effectively communicate in person and in writing. PLEASE NOTE THIS POSITION IS LOCATED IN FAIRFIELD, NJ. Relocation Assistance is provided.

Our client, a well-established company in the cosmetic and personal care industry, is looking for an Associate Chemist to join their team. This role operates fully onsite in their Clark, New Jersey location. Responsibilities: Assist with the formulation of cosmetic products, including batching, stability studies, and product evaluations. Conduct physicochemical characterizations, including pH, viscosity, rheology, and microscopy. Perform regulatory compliance assessments for raw materials and final formulations in alignment with industry standards. Operate lab equipment (e.g., rheometers, viscometers, microscopes) to assess product performance. Conduct quality control measurements and microscopic analysis. Required Qualifications: Bachelor's degree in Chemistry, Chemical Engineering, or a related scientific field. 0-3 years of professional experience in a laboratory environment (internships or academic projects in related fields are also considered). Previous experience in the cosmetic, pharmaceutical, or related industries is a plus. Strong proficiency in Microsoft Excel and other relevant computer programs. Experience with lab equipment (rheometers, viscometers, microscopes) is a plus. Ideal candidate will be quick learner, detail oriented with good communication skills and able to thrive in fast-paced team environment Strong attention to detail, organized, and methodical. If you meet the required qualifications and are interested in this role, please apply today. The Solomon Page Distinction Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve. About Solomon Page Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook, and LinkedIn. Opportunity Awaits.

6-month Contract Onsite in Piscataway, NJ Responsibilities: Analyze samples of finished products using chromatographic, spectroscopic, wet chemistry, and other analytical techniques Process analytical data and prepare reports to communicate results and findings to key stakeholders. Qualifications: Bachelor's degree in Chemistry 3+ years of Analytical Chemistry experience Experience in the cosmetics/consumer goods industry

Analyze samples of finished products using chromatographic, spectroscopic, wet chemistry, and other analytical techniques; process analytical data and prepare reports to communicate results and findings to key stakeholders. Qualifications: Position requires a Bachelor's degree in Chemistry 3+ years analytical chemistry Experience in cosmetics/consumer goods industry and good communication skills.

We're hiring an exceptionally talented Scientist specializing in hypertension, with a focus on in vitro models of hypertension and practical, innovative approaches to managing hypertension in a personalized medicine paradigm. Integrating hypertension knowledge at the molecular, cellular and systems levels to draw potential hypertension management insights will be critical in this role. At ICR, you'll get to: Develop practical and actionable interventions to manage hypertension Evaluate and improve existing hypertension management strategies Collaborate with other ICR scientists to leverage company resources and maximize productivity Please apply if you have: A PhD with 2+ years of post-graduate experience focused on molecular, cellular or systems-level hypertension research Experience with iPSC (induced pluripotent stem cell)-derived in vitro hypertension models Extensive knowledge of hypertension drugs and a good familiarity with world-wide anti-hypertensive drug development pipelines Clinical knowledge of hypertension measurement and management Even if you don't meet all these criteria, please apply anyway And you'll need: A friendly, easygoing personality The ability to work in the United States without sponsorship Compensation is commensurate with experience. The compensation ranges listed below are starting ranges. Starting base pay range: $135,000/yr - $185,000/yr Starting bonus range: $7,500/yr - $18,000/yr

Adecco is recruiting for an Analytical Chemist at a leading global cosmetic manufacturer in Piscataway, NJ. Apply today! Qualifications: Education: Bachelor's degree in chemistry. Experience: Minimum of 3 years in analytical chemistry, preferably within the cosmetics or consumer goods industry. Skills: Strong communication skills are essential. Pay Rate- The anticipated wage for this position is between $34 and $36.76 per hour. Hourly wage depends upon experience, education, geographic location, and other factors. Job Description: Analyze Samples: Utilize chromatographic, spectroscopic, wet chemistry, and other analytical techniques to analyze samples of finished products. Data Processing: Process analytical data and prepare comprehensive reports to communicate results and findings to key stakeholders. Work Hours: 8 AM - 5 PM Location: Piscataway, New Jersey PPE and Dress Code: Business Casual, work-appropriate attire. Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility

Industry: Pharmaceutical Research and Development We are seeking a highly skilled and motivated Formulation Chemist to lead and contribute to the development of oral liquid dosage forms. The ideal candidate will have expertise in taste masking, nanoparticle formulation, and scaling up to GMP manufacturing. You will collaborate with cross-functional teams to design, optimize, and implement robust formulations for clinical and commercial production. Key Responsibilities Formulation Development: Design and optimize oral liquid formulations, focusing on stability, bioavailability, and palatability. Incorporate taste-masking technologies such as encapsulation, polymer coatings, and flavor systems. Nanoparticle Formulation: Develop and characterize nanoparticle-based drug delivery systems to improve solubility and absorption. Scale-Up and GMP Manufacturing: Transition formulations from R&D to GMP manufacturing, ensuring scalability and regulatory compliance. Collaborate with manufacturing teams to troubleshoot and optimize production processes. Regulatory Support: Prepare documentation for regulatory submissions, including INDs, ANDAs, and 505(b)(2) NDAs. Ensure formulations comply with regulatory guidelines (FDA, ICH, etc.). Cross-Functional Collaboration: Work with analytical, quality assurance, and clinical teams to ensure successful project outcomes. Present technical findings and updates to stakeholders. Qualifications Education: Bachelor's, Master's, or Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field. Experience: Minimum 5 years of experience in pharmaceutical formulation development, particularly oral liquid dosage forms. Proven expertise in taste masking, including techniques such as encapsulation, particle size reduction, and polymer coatings. Hands-on experience with nanoparticle formulation and characterization is highly desirable. Familiarity with scaling up processes for GMP manufacturing. Knowledge of regulatory requirements for drug development (e.g., FDA, EMA). Skills and Competencies: Strong problem-solving skills and the ability to develop innovative solutions for formulation challenges. Proficient in using formulation and characterization equipment (e.g., high-shear mixers, spray dryers, particle sizers). Excellent project management and organizational skills. Effective communication skills for both technical and non-technical audiences. Preferred Qualifications: Experience with automated liquid filling systems and other manufacturing technologies. Knowledge of biopharmaceutical classification systems (BCS) and their application to formulation strategies. Understanding of controlled-release technologies and excipient compatibility studies. What We Offer: Competitive salary and comprehensive benefits package. Opportunities for professional development and growth within the organization. Collaborative and inclusive work environment. Access to state-of-the-art facilities and technologies. Equity participation in pre-IPO pharma / MedTech, commercial stage company

This position is for an experienced scientist with significant skills and interests in bench-level technical work. The individual will be part of a successful team focused on delivering innovation. Conduct laboratory bench research in the area of chromatography and sample preparation. Primary activities include execution of technical work under general supervision of senior technical staff. This will include carrying out chromatography sample preparation and testing as well as basic method development in GC. The ability to develop technical approaches and plans, solve appropriate technical problems and work independently is also expected. This position will require development of a detailed understanding of chromatographic theory. Key Responsibilities: Plan, setup and execute experiments Analyze data, accurately document experiments, propose next steps Follow safe laboratory practices and keep areas clean Participate in Department meetings and other R&D facility activities Requirements BS in Chemistry with 1-5 years of industry experience, or fresh MS in chemistry. Preferred: Familiarization with Agilent OpenLAB and ChemStation GC software.

LanceSoft is seeking a travel Cath Lab Technologist for a travel job in Brooklyn, New York. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 12 weeks 35 hours per week Shift: 11 hours, days Employment Type: Travel Cath lab and EP. Responsible for bedside CCL/EP procedures, circulating, documenting. No Call; No weekends 1:1 Ratio CCl has 3 rooms and EP lab 2 rooms PCI, Peripheral cases, diagnostic cases, Afib ablations, implants, AICD At least 2 yrs.; travel exp required BLS/ACLS #HCRKK8 About LanceSoft Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities. Benefits Weekly pay Medical benefits

Equiliem is seeking a local contract Cath Lab Technologist for a local contract job in Englewood, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 04/22/2025 Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Local Contract Cath Lab Tech Opportunity in Englewood, NJ! 4x10 Days - local 13 week contract REQUIRED: A minimum of 3 years of Cath lab experience required. RCIS or ARRT preferred. BLS required. Call/Text Amber with Equiliem ************ Email Resumes to ********************

AHS Staffing is seeking a travel Cath Lab Technologist for a travel job in Pequannock Township, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 05/12/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel AHS MedStat is looking for a Long Term (Travel) Radiologic Technologist Cardiac Cath Lab Tech in Pequannock Township, NJ. This assignment lasts 13 weeks and is scheduled to start on 2025-05-12T00:00:00.0000000 and run through 2025-08-15T00:00:00.0000000. Contracted travel position will have the possibility of being extended. True AHS Job ID #2142591. Posted job title: Radiologic Technologist Cardiac Cath Lab Tech About AHS Staffing At AHS Staffing, we are committed to providing a personalized, transparent, and rewarding experience. We go beyond the transactional nature of the industry by offering individualized job matching, clear communication, no-nonsense pay rates, and dedicated recruiter support 24/7. When you're on assignment with us, you'll get access to industry-leading benefits, including comprehensive medical coverage, 401(k) matching, competitive pay packages, licensure reimbursement, weekly pay, and more. Easily manage your day-to-day with our mobile app where you can view your assignment details, manage your compliance and licensing documents, submit timecards, and browse new jobs to land your next adventure. As a nationally recognized and award-winning agency, we understand the importance of providing a seamless experience from application to placement. Our top priority is matching you with assignments that align with both your personal and professional goals. Join us to experience working with an agency that truly prioritizes your success and well-being and see why thousands of healthcare professionals continue to trust us with their careers.

American Traveler is seeking a travel Cath Lab Technologist for a travel job in Denville, 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 American Traveler is offering a traveling Cardiac Cath Lab assignment in Denville New Jersey. Qualifications Current professional license as required by the state Proof of eligibility to work in the United States Valid BLS through the American Heart Association Specialty-related certifications are preferred and may be required for specific travel positions. RN positions require at least one year of recent experience in specialty and a like setting. American Traveler Benefits Customized compensation and benefits package Insurance coverage that suits your needs, including day one options Generous housing allowance or company-arranged accommodations Tax advantage options that can increase your take-home Travel and licensure reimbursements, referral bonuses, continuing education, and more American Traveler Job ID #P-471735. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About American Traveler With over 25 years of experience, American Traveler has established a reputation for outstanding customer service. Our team ensures a smooth, worry-free experience for those starting on or expanding their travel nursing and allied careers. With thousands of travel nursing and allied jobs nationwide, our attentive and approachable recruiters find positions that align perfectly with your career aspirations and personal requirements. American Traveler offers exceptional benefits, including premium medical, dental, vision and life insurance beginning day one of your assignment, generous 401(k) match, substantial housing stipends, and more. Additionally, with 24/7 support and access to our in-house clinicians, you are assured confidence and comfort throughout your assignment. With our team behind you, you can relax and enjoy a rewarding travel career. Benefits Weekly pay Medical benefits Referral bonus Discount program Dental benefits Vision benefits Continuing Education 401k retirement plan Mileage reimbursement

Host Healthcare is seeking a travel Cath Lab Technologist for a travel job in Englewood, 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 Host Healthcare is an award-winning travel healthcare company with an immediate opening for this Cath Lab Tech Position in Englewood, NJ. If you are interested in this position, please contact your recruiter and reference Job #2027035 Why choose Host Healthcare? Because a great Host provides a worry-free travel experience and always puts your needs first. Our passionate and transparent team members have made Host Healthcare the #1 ranked Travel Healthcare company in the U.S. Our recruiters act not only as your dedicated travel career mentor but also as your #1 advocate. When you work with us, you can trust that we will help you with everything from travel, to housing, and acting as a liaison between you and the facility. We've got your back! Travel Happy With Host Healthcare We offer the best pay for our travelers Day one medical, dental, and vision insurance License, travel, tuition, and scrub reimbursement Matching 401k Deluxe private housing or generous housing stipend Discounts to your favorite activities, restaurants, health & beauty brands, shopping and hotels Host Healthcare Job ID #a1fVJ000005U1LZYA0. 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: Cath Lab Tech About Host Healthcare At Host Healthcare, we provide a truly comfortable experience as you explore your travel nursing, therapy, or allied career. We make your travel healthcare journey easy by taking care of all the details, so you don't have to. We are on a mission to help others live better and we do this by helping the healers of the world be as comfortable as possible. With access to tens of thousands of travel nursing, therapy, and allied jobs in all 50 states, our responsive and friendly recruiters find your dream position based on what's important to you. During your assignment, get access to premium benefits, including Day 1 medical that continues up to 30 days between assignments, 401K matching, travel reimbursements, dedicated housing support, and more. We also offer 24/7 support from our team and access to our on-staff clinicians so you can feel comfortable and confident throughout your entire assignment. Travel comfortably with Host Healthcare. Benefits Referral bonus School loan reimbursement Vision benefits Wellness and fitness programs Company provided housing options License and certification reimbursement Life insurance Medical benefits Mileage reimbursement Pet insurance Discount program Employee assistance programs Guaranteed Hours Health savings account Holiday Pay 401k retirement plan Continuing Education Dental benefits

Key Responsibilities Conduct routine analysis of finished products and raw materials. Operate and troubleshoot laboratory instruments: HPLC, UPLC, GC, Karl Fischer, FTIR, visualization testers, and pH meters. Experience with chromatography software specifically Empower 3 for HPLC and UPLC analysis. Perform a range of tests, including assay, identity, content uniformity, blending uniformity, impurity testing, water content determination, content resolution, disintegration, and hardness testing, Follow approved testing procedures and methods according to internal SOPs and USP monographs. Report data accurately and promptly. Conduct peer data reviews and analyze data trends to ensure consistent results. Participate in laboratory investigations using TrackWise software Support routine lab activities such as balance calibration, pH calculations Perform stability testing of pharmaceutical products and excipients under ICH conditions, and assist with medical testing as necessary Position Requirement 4-8 years of hands-on experience in a laboratory setting, with a focus on oral solid dosage forms (tablets, capsules, sub-gels) and raw material Strong working knowledge of pharmaceutical testing, including stability testing, dissolution testing and compliance with USP standard Experience with laboratory instrumentation: HPLC, UPLC, GC, Karl Fischer, FTIR, and pH meter Prior experience with Empower 3 software

LanceSoft is seeking a travel Cath Lab Technologist for a travel job in New York City, New York. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 36 hours per week Shift: 9 hours, days, evenings, nights Employment Type: Travel Position: Cardiovascular Invasive Specialist (RCIS) - Cardiac Cath Lab Tech Location: New York, NY 10011 Required Qualifications: Registered Cardiovascular Invasive Specialist (RCIS) certification Minimum of 1 year of experience, including: Scrubbing cases and acting as first-assist BLS and ACLS certifications Shift Information: Shift Times: 8:00 AM - 6:00 PM, 4 days/week (Monday-Friday) Shift Length: 9 hours, 30 minutes Unpaid Meal Break: 30 minutes About LanceSoft Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities. Benefits Weekly pay Medical benefits

American Traveler is seeking a travel Cath Lab Technologist for a travel job in Livingston, New Jersey. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: Travel American Traveler is offering a traveling Cardiac Cath Lab assignment in Livingston New Jersey. Qualifications Current professional license as required by the state Proof of eligibility to work in the United States Valid BLS through the American Heart Association Specialty-related certifications are preferred and may be required for specific travel positions. RN positions require at least one year of recent experience in specialty and a like setting. American Traveler Benefits Customized compensation and benefits package Insurance coverage that suits your needs, including day one options Generous housing allowance or company-arranged accommodations Tax advantage options that can increase your take-home Travel and licensure reimbursements, referral bonuses, continuing education, and more American Traveler Job ID #P-528383. Pay package is based on 12 hour shifts and 36 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About American Traveler With over 25 years of experience, American Traveler has established a reputation for outstanding customer service. Our team ensures a smooth, worry-free experience for those starting on or expanding their travel nursing and allied careers. With thousands of travel nursing and allied jobs nationwide, our attentive and approachable recruiters find positions that align perfectly with your career aspirations and personal requirements. American Traveler offers exceptional benefits, including premium medical, dental, vision and life insurance beginning day one of your assignment, generous 401(k) match, substantial housing stipends, and more. Additionally, with 24/7 support and access to our in-house clinicians, you are assured confidence and comfort throughout your assignment. With our team behind you, you can relax and enjoy a rewarding travel career. Benefits Weekly pay Medical benefits Referral bonus Discount program Dental benefits Vision benefits Continuing Education 401k retirement plan Mileage reimbursement