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🔬 Scientist – Biopharma Services Title Level Commensurate with Experience (Senior Associate Scientist II or Scientist I) 📍 Location: South Plainfield, NJ Admera Health is hiring a Scientist to join our Biopharma Services team in South Plainfield, NJ. This is a hands-on, lab-based role supporting high-impact research in genomics and next-generation sequencing (NGS). We are open to hiring at either the Senior Associate Scientist II or Scientist I level depending on your background. Title and responsibilities will align with your education, experience, and demonstrated capabilities. 🧬 About Admera Health Admera Health – Entering the ADvanced Molecular ERA Admera Health is a genomic and bioinformatics research services company supporting pharmaceutical and biotech clients from early discoveries through clinical research. Our areas of expertise include genomics, transcriptomics, epigenomics, and advanced bioinformatics. We specialize in working with challenging sample types, such as FFPE, single-cell, and low-input materials, and offer tailored solutions across a wide range of platforms. 🌟 Why Join Us? We’re proud of our innovative, energetic, and collaborative culture. Our values: • Innovation, • Accountability, • Customer focus, • Results orientation, • Team-driven success 🧪 What You’ll Be Doing • Perform molecular biology and NGS workflows (e.g., RNA-seq, WGS, WES), • Maintain accurate and thorough documentation of experiments and outcomes, • Collaborate cross-functionally with project managers and scientific teams, • Contribute to troubleshooting and continuous workflow improvement, • Ensure timely, high-quality project delivery in a fast-paced R&D environment 📈 Role Levels and Expectations 🔹 Senior Associate Scientist II • Execute experiments with guidance, • Participate in troubleshooting and basic protocol refinement, • Assist with documentation, data review, and internal communications, • Support project timelines and collaborate with teammates, • Independently design, troubleshoot, and optimize experiments, • Lead training and mentoring of junior staff on techniques, documentation, and SOPs, • Contribute to or lead workflow development and process innovation, • Present results to internal stakeholders and clients, • Serve as a technical resource across departments 🎓 Qualifications • M.S. or Ph.D. in Biological Sciences or a related field, • For Senior Associate Scientist II: Typically 2–3 years of hands-on lab experience, • For Scientist I: Typically 5+ years of lab experience or a Ph.D. with industry exposure, • Strong background in molecular biology techniques (e.g., PCR, cloning, sequence analysis), • Experience with NGS platforms (e.g., Illumina) strongly preferred, • Excellent documentation, communication, and organizational skills, • Experience in research-focused or biopharma service environments preferred 💵 Compensation • Salary Range Starting at: $70,000 annually (commensurate with experience and qualifications), • Bonus Eligibility: Performance-based discretionary bonus, • Comprehensive health, dental, vision, and retirement benefits, • Paid time off and holiday schedule, • Ongoing professional development support 🌐 How to Apply For more information, please visit . To review and apply to our open positions, visit: 🤝 Equal Opportunity Employer Statement Admera Health is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Company Description At MedCore Research, we are redefining the future of clinical trials with a decentralized, patient-centric, and technology-driven approach. Our mission is to accelerate medical advancements by delivering efficient, high-quality, and compliant research solutions. We specialize in early to late-phase trials, offering customized, scalable, and regulatory-compliant solutions for pharmaceutical, biotech, and medical device companies. Our decentralized clinical trial (DCT) model enhances patient accessibility, engagement, and retention, ensuring data integrity and compliance, to bring life-changing treatments to patients faster. Location: Irvington, NJ (Onsite) Schedule: 3 days per week, 10:00 AM – 4:00 PM Role Description We are seeking a dedicated and detail-oriented Part-Time Nurse to support our clinical trial site in Irvington, NJ. This role is ideal for a nurse interested in expanding into clinical research, providing hands-on support for the safe and efficient conduct of clinical trials. As part of the clinical team, you will assist in patient care, protocol adherence, and site operations while learning the unique aspects of clinical trial management. Key responsibilities include: • Supporting investigators and coordinators with patient visits during clinical trials., • Performing vital signs, sample collection, and drug administration per protocol and scope of practice., • Monitoring and documenting adverse events and patient safety data., • Assisting with drug accountability and maintaining proper storage conditions., • Recording and maintaining temperature logs and compliance documentation., • Ensuring accurate source documentation and assisting with regulatory paperwork., • Collaborating with research staff to maintain compliance with ICH/GCP guidelines. Qualifications • Licensed Registered Nurse (RN) or Licensed Practical Nurse (LPN) in the state of New Jersey., • Minimum 1 year of clinical experience in a healthcare or patient care setting., • Strong interest in clinical research and clinical trials., • Excellent organizational, communication, and documentation skills., • Ability to work independently while collaborating effectively with a multidisciplinary team., • Prior clinical research experience is a plus but not required (training provided)., • Proficiency with Microsoft Office (Word, Excel, Outlook). ✨ This role offers nurses the chance to transition into the growing field of clinical research, gaining valuable experience in trial operations while maintaining a flexible, part-time schedule.

Job Description Seeking a Swiss CNC Programmer for our client, a leading manufacturer specializing in precision components for the medical device industry. Type: Contract-to-hire Location: Union County, NJ Pay: $35 - $39/hr Shift: Monday - Friday, 7am - 3pm Duties: * Program, set up, and operate a range of CNC machines, including Wire EDM, CNC Mills, and CNC Grinders. * Translate detailed technical drawings into accurate, high-quality components. * Support cost reduction initiatives once parts are in production. * Manage full setups, tool changes, and machine adjustments to maintain quoted cycle times. * Inspect parts using both contact and non-contact methods to confirm surface finish, concentricity, straightness, and other key tolerances. * Design and develop tooling for complex component geometries. * Troubleshoot setup and production issues to keep output on schedule and within quality standards. * Provide input for new part estimates, including setup/cycle times, tooling requirements, and scrap considerations. * Collaborate closely with Quality, Manufacturing, and Engineering teams to resolve production challenges and support quoting efforts. * Maintain compliance with safety standards and company operating procedures. • Perform machine and bar feeder troubleshooting; work with outside vendors when necessary. Qualifications: * Minimum of 5 years of hands-on CNC programming, setup, and operation experience. * Background in regulated manufacturing environments (ISO 9001, ISO 13485, or similar). * Familiarity with Lean Manufacturing practices and process improvement methods. * Strong mechanical aptitude with the ability to troubleshoot complex machining challenges. * Analytical thinker who can evaluate problems, identify solutions, and work well in collaborative problem-solving environments. * Consistently meets production standards while maintaining accuracy and quality. * Skilled in precision machining with a focus on meeting both internal and customer-driven quality standards. * Proficiency with CAM software (FeatureCAM, PartMaker, or similar) and CAD platforms such as SolidWorks. * Ability to edit CNC programs, adjust offsets, and perform complete setups. • Excellent communication and teamwork skills, with the ability to collaborate effectively across all levels of the organization. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! Company DescriptionSince 1995 Astrix has been delivering information technology consulting, regulatory advisory services and staffing solutions to the scientific community. We can assist in augmenting your internal resources to deliver optimum solutions on time and within budget. It is our goal to simply do it right. We work everyday to create value and build trust with our clients, employees, partners and vendors. Astrix provides scientists to a broad spectrum of scientific based industries including: Chemical, Biotech, Pharmaceutical, Cosmetics, Food Science, Flavors and Fragrances, Biomedical, Consumer Products, Environmental, Medical device, Petrochemical and Clinical Research.Since 1995 Astrix has been delivering information technology consulting, regulatory advisory services and staffing solutions to the scientific community. We can assist in augmenting your internal resources to deliver optimum solutions on time and within budget. It is our goal to simply do it right. We work everyday to create value and build trust with our clients, employees, partners and vendors.\r\n\r\nAstrix provides scientists to a broad spectrum of scientific based industries including: Chemical, Biotech, Pharmaceutical, Cosmetics, Food Science, Flavors and Fragrances, Biomedical, Consumer Products, Environmental, Medical device, Petrochemical and Clinical Research.

Job DescriptionQBench is the modern operating system for testing labs. We help scientific laboratories scale faster, reduce errors, and ship results seamlessly by replacing legacy systems with a highly configurable, cloud-native LIMS (Laboratory Information Management System). Our customers are doing everything from detecting food-borne pathogens to enabling cutting-edge molecular diagnostics — and we’re helping them do it faster and better. Why You’ll Love Working with Us: * Shape the Future of Lab Software: As a Product Designer at QBench, your work won’t just make our product look better — it will shape how scientists, technicians, and researchers work every day, helping them deliver faster, more accurate results that drive innovation. Career Growth: We’re committed to your professional development, offering continuous learning opportunities, mentorship, and the chance to lead strategic design initiatives. Collaborative Culture: Work with a tight-knit, cross-functional team that values curiosity, creativity, and your unique perspective. Your input will influence not only design but also product direction. Competitive Compensation: We offer a strong salary package and benefits designed to support your financial and personal well-being. Remote Flexibility: Enjoy the freedom of a fully remote role while still feeling connected to a motivated, mission-driven team. About the Role We’re looking for a talented Product Designer to join our growing product team and help shape the future of laboratory software. You’ll work closely with the product manager, engineers, and subject matter experts to research, design, and iterate on intuitive, elegant user experiences that solve complex problems for our customers. You’ll blend design craft with product thinking, and have ownership of features from concept to final polish, ensuring they are both delightful to use and highly functional. What You’ll Do * Conduct user research to deeply understand customer needs, workflows, pain points, and synthesize findings to guide design decisions. * Translate insights into end-to-end feature designs that align with both user goals and business priorities. * Translate concepts into user flows, wireframes, interactive prototypes, and high-fidelity mockups that lead to intuitive user experiences. * Collaborate with product and engineering to ensure designs are feasible, scalable, and implemented with high quality. * Take a user-centric design approach and iterate based on feedback and conduct usability testing to continually improve the product’s user experience. * Identify user experience challenges and design solutions that improve the overall UX for customers. * Make strategic design and user-experience decisions related to old and new features. * Advocate for design best practices and user needs while balancing technical and business constraints. * Contribute to our new and evolving design system. What We’re Looking For * 3-5 years of experience designing SaaS products, ideally in complex or technical domains. * A strong portfolio showcasing visual design excellence, and UI/UX and product thinking. * Proficiency in Figma and modern design practices. * Experience working from problem definition through to shipped product. * Strong understanding of user-centered design principles, accessibility, and responsive design. * Experience designing workflow software and dashboards. * Excellent communication skills and ability to work cross-functionally. * Demonstrated ability to collaborate in a remote-first environment. * Able to work within US-based time zones. Nice to Have * Experience designing for enterprise or B2B software. * Familiarity with laboratory workflows or LIMS platforms. * Experience designing compact applications that are highly configurable for power users. * Experience in regulated domains (e.g. HealthTech, Biotech, Life Sciences) Powered by JazzHR KMwmYSpQWh

Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success. The Experience With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents. We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn. At PSC Biotech®, it’s about more than just a job—it’s about your career and your future. Your Role We are excited to accept applications for future opportunities. Join our talent pool for future openings by applying now. This is a W2-Temp 6-month role with potential FTE extension.We are seeking a highly skilled and detail-oriented Quality Assurance Engineer to join our team in the life science sector. The ideal candidate will have a strong background in quality assurance processes, with specialized experience in auditing, ensuring compliance with regulatory standards, and maintaining the highest quality standards in pharmaceutical production. This individual will play a crucial role in the review and assessment of manufacturing practices, quality control systems, and regulatory compliance within a highly regulated environment. • Develop, implement, and maintain quality assurance processes and procedures in alignment with industry standards and regulations., • Ensure all manufacturing processes comply with relevant regulations, including but not limited to FDA, EMA, ICH, and GMP guidelines., • Review batch records, validation documentation, and quality control data to ensure compliance and product quality., • Conduct internal and external audits to assess compliance with Good Manufacturing Practices (GMP), FDA regulations, and other relevant standards., • Collaborate with cross-functional teams to ensure effective implementation of audit findings and continuous improvement initiatives., • Prepare detailed audit reports, CAPA (Corrective and Preventive Actions) reports, and other documentation as required., • Maintain thorough and accurate records of quality assurance activities, audits, and regulatory communications., • Participate in the preparation and review of SOPs, work instructions, and other quality-related documents., • Lead or participate in continuous improvement initiatives, focusing on quality and operational efficiency. Requirements • Bachelor's degree in engineering or related technical field., • Minimum of 5+ years of experience in quality assurance within the life science industry., • Proven experience in conducting GMP audits, both internal and external, in a pharmaceutical or life sciences environment., • Experience with regulatory bodies such as the FDA, EMA, and other international regulatory agencies., • Familiarity with Quality Management Systems (QMS), CAPA, deviation management, and risk management., • Strong understanding of GMP regulations, FDA guidelines, and other applicable industry standards., • Excellent analytical and problem-solving skills., • Exceptional attention to detail and ability to identify potential areas of risk and non-compliance., • Strong verbal and written communication skills, with the ability to prepare clear and concise reports., • Travel is required. At PSC Biotech, many of our projects and clients are located in various regions around the country. Therefore, we value candidates who are willing and able to travel as needed for project assignments and client engagements. The ability to adapt to different locations, cultures, and work environments is essential, as it allows our team members to collaborate effectively with clients and colleagues nationally. Equal Opportunity Employment Statement PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law. #LI-RW1 BenefitsW2 Temp positions include our medical and sick time benefits. Adhering to the requirements of New Jersey's law on salary transparency, the salary bracket for this role is set between $100,000 - $115,000 annually. The offered salary may be adjusted based on various factors such as the applicant's qualifications, skills, and professional experience.

Job Description Location: Flexible U.S. Offices | Hybrid Work Environment Summary Foley & Lardner’s nationally recognized Chemical, Biotechnology & Pharmaceutical group is seeking a Patent Agent or Patent Attorney with a Ph.D. in life sciences to support its growing portfolio of biotech and pharmaceutical clients. This is an exceptional opportunity to work with cutting-edge innovations and a top-tier legal team known for strategic IP counsel. Ideal for professionals with strong scientific backgrounds and a passion for life sciences, patent law, and client-facing advisory work. Key Responsibilities * Draft and prosecute U.S. and international patent applications in the biotechnology and life sciences sectors * Conduct patentability, freedom-to-operate, and due diligence analyses * Advise clients on IP strategy, portfolio management, and patent lifecycle issues * Collaborate with partners and senior attorneys on patent opinions and litigation strategy support * Engage in client communication and USPTO correspondence * Stay informed on developments in biotech IP law and relevant case precedents * Participate in internal training and contribute to knowledge sharing across the team Qualifications * Ph.D. in Molecular Biology, Biochemistry, Chemistry, Genetics, or a closely related life sciences field * Minimum 3 years of experience in patent drafting and prosecution * USPTO registration is required * Experience preparing patent opinions (preferred) * Strong legal research, technical writing, and client communication skills * Law firm or IP agency background preferred * Demonstrated ability to counsel clients and manage workflow independently * Excellent academic credentials Please Do Not Apply If You: * Do not have direct experience in biotech or pharmaceutical patent drafting/prosecution * Are unwilling to develop subject-matter depth in the life sciences IP space * Avoid direct client interaction or prefer to work in isolated, non-collaborative environments * Are not open to working in a fast-paced, high-performing team * Cannot commit to timely bar admission in Florida (if applicable to your location) Interview Process * Resume & Academic Transcript Review * Initial Screen with IP Team * Technical Interview or Writing Sample Evaluation * Interview Panel with Senior Patent Attorneys and Partners * Final “Office Fit” Discussion & Offer

Computer System Validation (CSV) experience in regulated pharmaceutical and biotech environments, with strong knowledge of GAMP 5, 21 CFR Part 11, and Computer Software Assurance (CSA) principles. This position will drive computer system validation activities for the Summit site Manufacturing Execut

The Account Executive, Cell & Gene Therapies (CGT), is responsible for driving strategic sales growth and market penetration of Fresenius Kabi's CGT technologies across the U.This role builds and manages key relationships with academic, biotech, and pharmaceutical stakeholders, identifies new busine

Job Description SENIOR CONSTRUCTION MANAGER WHO WE ARE We’re Genesis AEC – an award-winning architecture, engineering, construction management, and CQV firm and a leader in the life sciences industry. Ranked #5 in Pharmaceutical Design by ENR magazine, we’re designing and constructing facilities that advance worldwide health. We’re proud to contribute to our clients’ success, earning honors that include a 2021 ISPE Facility of the Year (FOYA) award and an ENR Mid-Atlantic’s Best Manufacturing Project award for our work at the National Institutes of Health. Our culture is based on inclusion, embracing all identities, backgrounds, and perspectives. When you’re on our team, you’ll find you are supported, challenged, and encouraged to grow, with opportunities, training, and a work-life balance to help you succeed. Description Assigned to a project team, reporting directly to the project manager, and is responsible for supporting the team during all phases of a construction project. Individuals must be motivated self-starters who possess strong organizational and communication skills while working under strict time deadlines in an ever-changing environment. Projects consist of renovations and new construction for pharmaceutical and institutional facilities. Qualified candidates will be on job sites during construction and will be responsible for the daily operations of construction. These responsibilities include: • Develop and manage the site safety and logistics plans, • Develops and manages the project schedule, • Complete job safety documentation as required by the corporate safety program, • Oversee the work of vendors and subcontractors to ensure compliance with quality requirements, • Manages all stages of construction, • Scheduling and managing subcontractors, • Monitor plans and material take-offs for work in place values, • Perform site inspections, evaluations, and provide a report of those inspections, • Support the Project Manager in coordination meetings with trade subcontractors onsite, • Performance of the duties may require physical ability to climb permanent and temporary stairs, walk distances, climb ladders, and otherwise negotiate work areas under construction. Specific vision abilities required by this job include close vision, peripheral vision, depth perception, and the ability to adjust focus., • Performing this job requires the use of hands to handle, or feel objects, tools, or controls, sit, talk, and hear (bells, whistles, etc.), stand, climb, balance, stoop, kneel, crouch, or crawl. While performing the duties of this job, the employee works on-site at the construction worksite where the employee is regularly exposed to moving mechanical parts; high precarious places, fumes or airborne particles, and outside weather conditions. The noise in this work environment is usually moderate to very loud. May perform other duties as necessary or assigned. Training: • OSHA 30-hour training must be completed within 5 years, or can be completed upon hire., • A bachelor's degree is preferred but not required., • 10+ years of experience in managing facility construction in the Pharmaceutical, Biotech, and Healthcare industries is required, • Experience in the life sciences and design-build industry is preferred, • Travel will be required to project sites in the Mid-Atlantic region. However, we do our best to keep our people close to home., • A valid driver's license and reliable transportation are required., • Experience in the life sciences and design-build industry is preferred, • Procore experience preferred, • Our collaborative and positive culture sets us apart, • We offer schedule flexibility. *For field-based personnel, flexible scheduling may be subject to client/project site requirements., • Comprehensive medical, dental, vision, and RX insurance plans, with two-thirds of your premiums and deductible paid!, • Competitive 401 (k) match program, • Generous paid time off, • Thought leadership opportunities, including a $1,000 award for presenting or publishing your technical expertise!, • Competitive company-paid training opportunities, • A 5% salary increase for earning your professional license!, • Endless opportunities to grow your career Genesis is dedicated to supporting professional development in a welcoming work environment. Our collaborative culture ensures that our clients benefit from top-tier work across our entire range of professional offerings. At Genesis, we believe that hard work and achievement are integral to a balanced and rewarding life. As our single most valuable asset, we make sure our employees know that we appreciate them. At Genesis, you will find people from many different backgrounds and with very different interests all working together to achieve a common goal.Join our team at Genesis, where we have the privilege of contributing to worldwide health through the design and construction of facilities where science is conducted and life-saving drugs are manufactured. This is a tremendous opportunity for a dedicated individual who wants to contribute to our client’s success, as well as our impressive growth.\r\n\r\nGenesis is dedicated to supporting professional development in a welcoming work environment. Our collaborative culture ensures that our clients benefit from top-tier work across our entire range of professional offerings.\r\n\r\nAt Genesis, we believe that hard work and achievement are integral to a balanced and rewarding life. As our single most valuable asset, we make sure our employees know that we appreciate them. At Genesis, you will find people from many different backgrounds and with very different interests all working together to achieve a common goal.

Private Practice, Outpatient/Inpatient.Experienced Physician preferred.Unique opportunity to blend clinical and research responsibilities.Hematologist and Clinical Investigator.Young to mid-career clinical researcher with a strong background in providing direct patient care and conducting clini

Host Healthcare is seeking a travel Medical Technologist for a travel job in New York, New York.Job Description & Requirements.Host Healthcare Job ID #a1fVJ0000076Lk6YAE.Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determine

RWJBarnabas Health and Rutgers Robert Wood Johnson Medical School (RWJMS), Department of Pathology and Laboratory Medicine, are seeking a Medical Director for the Laboratory at Robert Wood Johnson University Hospital-Hamilton.This leadership role provides oversight of all anatomic and clinical labor

Interest in the dynamic world of life sciences, including biotechnology, pharmaceuticals, digital health, medical devices, diagnostics, and discovery tools.

Gastroenterologist - Director of Inflammatory Bowel Disease.Jersey Shore University Medical Center - Neptune, New Jersey.Jersey Shore University Medical Center in Neptune, New Jersey as the Director of Inflammatory Bowel Disease (IBD).Successful candidates will have a passion for clinical and academ

RWJBarnabas Health and Rutgers Robert Wood Johnson Medical School (RWJMS), Department of Pathology and Laboratory Medicine, are seeking a Medical Director of Pathology/Transfusion Medicine to provide leadership and expertise in transfusion medicine at Robert Wood Johnson University Hospital in New B

Health Advocates Network - Allied is seeking a travel Cath Lab Technologist for a travel job in Newark, New Jersey.Job Description & Requirements.Health Advocates Network is hiring a Cath Lab/ Cardiovascular Technologist with.This is a full-time contract position at a nationally recognized hospital

Director of Bone Marrow Transplant .Jersey Shore University Medical Center - Neptune, New Jersey.Board Certified/Board Eligible Infectious Disease physician to serve as the founding Director of the new Bone Marrow Transplant (BMT) Infectious Disease Program at Jersey Shore University Medical Ce

Capital Healths Hematology Oncology Specialist Team Seeks Full Time Hematologist Oncologist.The Capital Health Hematology Oncology Specialist team is strongly committed to caring for the whole patient and places special emphasis on providing patient-centered care.This open role is an opportunit

Strategic Deployment Manager, Life Science.We're looking to hire a Strategic Deployment Manager to join us in our mission to improve human health and quality of life through the development, distribution, and application of advanced computational methods!.As a member of our Enterprise Informatics te

Job Description Health Advocates Network - 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 - Start Date: 11/10/2025 - Duration: 13 weeks - 36 hours

RWJBarnabas Health, the largest integrated healthcare system in New Jersey, is currently seeking an experienced and dynamic leader in Acute Care Surgery Program at Monmouth Medical Center (MMC) in Long Branch, NJ.This is an exciting opportunity for a visionary leader to develop and grow an evolving

ALOIS Healthcare is seeking a travel Cath Lab Technologist for a travel job in Newton, New Jersey.Job Description & Requirements.The Cardiac Cath Lab Tech performs advanced diagnostic and interventional cardiac procedures, peripheral vascular procedures, and structural heart procedures in the Cardia

RWJBarnabas Health, New Jerseys largest integrated healthcare system, is seeking board-certified/board-eligible.New staff will be joining a group of 19 anesthesiologists and 20 CRNAs.Successful candidates must be:.ABA board-certified or board-eligible for new graduates.Completed Anesthesiology resid

Accenture Song accelerates growth and value for our clients through sustained customer relevance.Our capabilities ideation to execution: growth, product and experience design; technology and experience platforms; creative, media and marketing strategy; and campaign, content and channel orchestration

RWJBarnabas Health, the most comprehensive health care delivery system in New Jersey, is seeking board-certified Hematologists/Oncologists in Hamilton and Toms River, NJ.These unique positions offer an opportunity to work closely with the Rutgers Cancer Institute of New Jersey, the states only

The ideal candidate will have substantial law firm experience representing biotechs and big pharmas as they license patents and collaborate to advance novel therapeutics, vaccines, diagnostic and digital health technologies through clinical trials and toward regulatory (FDA) approval.

Senior Director - Healthcare & Life Sciences/ Pharma & Biotech. Our Healthcare & Life Science Division works across the highly innovative, complex healthcare sector, including pharmaceuticals & biotech, medical technology, diagnostics, digital health & healthcare IT, healthcare B2B, providers, consu

Conduct research and analysis on diverse technologies, including biotechnology, pharmaceuticals, medical devices, digital health, fintech, AI, IT, edtech, renewable energy, AR/VR, and cybersecurity.

Those arent words that are usually associated with a job.But working at Bristol Myers Squibb is anything but usual.Here, uniquely interesting work happens every day, in every department.From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the li

Corporate And Business Strategy Manager.A career within Corporate and Business Strategy services will provide you with the opportunity to help our clients solve their toughest problems and seize essential advantages by defining and evaluating strategies of all types.We analyse business and market tr

Springboard Healthcare is seeking a travel Cath Lab Technologist for a travel job in Pompton Plains, New Jersey.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 10/06/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours Employment

Little Healthcare And Life Sciences Manager.Little (ADL), founded in 1886 as the world's first consulting firm, continues to redefine business strategy, technology, and innovation.Today, ADL is a global partnership with 1,500+ consultants in 40 offices across 30+ countries.Boston, New York, and San

Health Advocates Network - Northeast 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: 10/17/2025 Duration: 12 weeks 36 hours per week Shift: 12 hours Em

Global Account Manager For Life Sciences.As a Global Account Manager for Life Sciences (LS), you will have the exciting opportunity to help drive the growth and shape the future of an emerging technology.Your responsibilities will include identifying great ways to improve outcomes for customers, dri

Springboard Healthcare 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: 10/20/2025 Duration: 13 weeks 40 hours per week Shift: 8 hours Employment Typ

This is a hybrid role, with the expectation that time working will regularly take place inside and outside of our Boston or New York office.Together, Silicon Valley Bank and First Citizens offer you the strength and stability of a diversified financial institution with a 125-year tradition of servic

Sr Enterprise Account Executive - Health And Life Sciences.It all started in sunny San Diego, California in 2004 when a visionary engineer, Fred Luddy, saw the potential to transform how we work.Fast forward to today ServiceNow stands as a global market leader, bringing innovative AI-enhanced techn

Planet Healthcare 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: 10/06/2025 Duration: 12 weeks 40 hours per week Shift: 8 hours Employment Type: Trave

Vice President, Global Lead Biotherapeutics Engineering.Johnson & Johnson Innovative Medicine is recruiting for a Vice President, Global Lead Biotherapeutics Engineering located in Wilson, North Carolina or Raritan, New Jersey.The Global Lead of Site Engineering will be a key leadership role respons

Senior Executive Director of Clinical Development in Hematology.Join a rapidly growing pharmaceutical developer making strides in innovative medical solutions.The company seeks a Senior Executive Director to lead Clinical Development in Hematology.In this influential position, you will provide essen

Triage Staffing 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: 10/27/2025 Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type:

Executive Director, Translational Biology.Recursion is looking for a highly collaborative, strategic, and experienced translational biology leader to guide a future-driven, technology-oriented approach to robust preclinical data packages.We're focused on identifying and validating innovative drugs w

PRN Healthcare 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: 10/13/2025 Duration: 13 weeks 36 hours per week Shift: 12 hours, days Employment Type: T

Client Partner - Healthcare & Life Sciences.It's fun to work in a company where people truly BELIEVE in what they are doing!.We're committed to bringing passion and customer focus to the business.Fractal is a strategic AI partner to Fortune 500 companies with a vision to power every human decision i

Embryology Lab Assistant Manager.The Embryology Lab Assistant Manager supervises daily clinical embryology procedures and maintains IVI RMA's Lab Philosophy, Mission, and Performance Standards.This position is also responsible for the implementation of quality assurance/control programs, regulatory

Director New Product Planning - Oncology.The Director, New Product Planning (NPP) reports to the Head of NPP within the Oncology franchise.He/she will support the NPP leads as the primary commercial liaison with program teams within the Oncology development organization, responsible for providing co

Bachelor's Degree required in Chemistry, Biochemistry, or Biotechnology related scientific discipline and 5-7 years of working experience and 2 years managing laboratory analysts in an FDA-regulated biotechnology, pharmaceutical company are required. Master's degree in Chemistry, Biochemistry, or Bi

PRIDE Health is seeking a travel Histology Technologist for a travel job in New York City, New York.Job Description & Requirements.A Histotechnologist prepares tissue samples for examination under a microscope.Responsibilities include processing, embedding, and sectioning tissue samples, ensurin