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Job Title: Medical Laboratory Scientist Location: Clifton, NJ Duration: 03+ Months Shift/Time Zone: Fri, Sat 12pm-8:30pm Is Covid Vaccination Required? Is Position Eligible for Remote Work? No State of Credentials Licenses Required: No Is this a hospital site that requires additional credentialing? No Job Responsibilities: 1. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result;, 2. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens;, 3. Analyze specimens using approved testing procedures (see department SOPs)., 4. Review and release test results., 5. Follow CLIA, HIPAA, OSHA, and safety guidelines as described in their respective guidelines., 6. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and all maintenance performed;, 7. Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance., 8. Identify problems that may adversely affect test performance or reporting of test results, correct the problems encountered or immediately notify the senior technologist or supervisor., 9. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications., 10. Follow department's procedure in reporting STATS or Critical results to clients., 11. If applicable, answer questions from customers or other lab personnel., 12. Maintain complete records of all testing performed on-site., 13. Maintain general appearance of the department., 14. Make sure reagents/test kits have received dates, expiration dates, and if applicable opened dates. 15. Review/train on new procedures., 15. Attend monthly department and any additional training/educational meetings., 16. Participate in all applicable safety training sessions. Know the location and contents of the safety manual. Know the location/use of all applicable safety equipment., 17. If needed, participate in government or regulatory agency inspections., 18. Perform other duties as directed by supervisor. Required Knowledge: A solid understanding of basic laboratory testing is required for this position. The successful candidate must possess good computer skills and be able to adapt to working in multiple computer systems. Must have knowledge of QC and QA as well as knowledge of all areas of the laboratory. Education: BS in Medical Technology preferred; or BS/BA in Chemistry or Biology, or Associates degree in a Laboratory Science or Medical Technology, or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990. Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation). United States educated candidates must provide a detailed original transcript. A successful candidate should possess or be eligible for national certification as an MT / MLT from a recognized organization (ASCP or AMT). Work Experience: 01-year Clinical experience (high complexity testing) preferred. Minimum of 1 year of clinical laboratory experience in highly complex testing for those with BS/BA in Chemistry or Biology. National and State licensure as required. Special Requirements: 1. Must have the ability to establish work priorities and handle several procedures simultaneously., 2. Must interact with other departments., 3. Contact with clients may be required, good customer service skills are important., 4. Must protect patient confidentiality at all times.

Job Description Why Join Us At Paradromics Inc., we’re redefining what’s possible in neurotechnology to restore independence and transform lives. As a leader in brain–computer interface (BCI) innovation, Paradromics is developing high-data-rate neural communication systems that empower people with paralysis, sensory loss, and neurological conditions to reconnect with the world. Join a mission-driven team where data, science, and technology converge and where your analytical expertise will directly contribute to building life-changing breakthroughs in human communication. About Paradromics Paradromics Inc. is a pioneering medical technology company dedicated to developing implantable brain–computer interfaces that restore communication and functional independence for people affected by severe neurological conditions. Our work sits at the intersection of neuroscience, engineering, and data science. Headquartered in Austin, Texas, Paradromics operates with a global, remote-first mindset empowering top talent to contribute from anywhere. Our culture thrives on innovation, collaboration, and scientific excellence, where data-driven insights accelerate our mission to build a more connected future. Position Summary The Senior Data Scientist will play a key role in advancing Paradromics’ data science capabilities by designing and deploying machine learning and signal processing models that drive our neurotechnology systems. You will work with large-scale neural and behavioral datasets to uncover insights, develop predictive models, and enhance the performance of our brain–computer interface (BCI) platforms. The ideal candidate is a hands-on problem solver who thrives in a collaborative, cross-functional environment passionate about applying data science to unlock new frontiers in neuroscience and human health. Key Responsibilities • Design, develop, and optimize machine learning models and statistical algorithms to analyze complex neural and behavioral data., • Collaborate with neuroscientists, software engineers, and hardware teams to integrate data-driven solutions into product development., • Build scalable data pipelines and tools for data acquisition, analysis, and visualization., • Conduct exploratory data analysis and interpret high-frequency neural signals to identify actionable patterns., • Support development of real-time decoding algorithms for BCI applications., • Ensure scientific rigor, reproducibility, and documentation across all analytical workflows., • Communicate findings effectively to both technical and non-technical stakeholders., • Contribute to long-term data infrastructure and strategic planning for advanced AI applications. Qualifications • Bachelor’s or Master’s degree in Data Science, Computer Science, Applied Mathematics, Electrical Engineering, Neuroscience, or a related field., • 5–8 years of professional experience in data science, machine learning, or computational modeling, preferably within biomedical, neuroscience, or high-tech environments., • Proficiency in Python and related libraries (NumPy, Pandas, Scikit-learn, TensorFlow, or PyTorch)., • Strong foundation in statistics, signal processing, and machine learning methodologies., • Experience working with time-series, biosignal, or neural data., • Strong skills in data visualization and communication (Matplotlib, Plotly, or Dash)., • Proven ability to work independently and collaboratively in a remote, cross-functional environment. Preferred Qualifications • Ph.D. in Data Science, Computational Neuroscience, Electrical Engineering, or related discipline., • Experience with neural recording technologies (EEG, ECoG, or intracortical data)., • Familiarity with cloud computing platforms (AWS, GCP, or Azure)., • Knowledge of deep learning architectures for decoding or pattern recognition tasks., • Prior experience in neurotechnology, medical devices, or healthcare R&D. Work Environment • Fully remote position (U.S.-based), with flexibility for collaboration across time zones., • Occasional travel may be required for team meetings, research collaborations, or conferences.

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

Job DescriptionQuality Control Manager The Quality Control (QC) Manager plays a pivotal role in ensuring that QC is effectively serving in its support role to clinical and commercial production. The QC Manager will ensure that analytical testing for process check points, stability, and release assays are being carried out to certify that quality standards are upheld for all products produced at the facility. The goal is to ensure that the Quality Control group and company is constantly moving towards fulfilling its short-term and long-term objectives and does not diverge from its strategic guidelines. Under the direction of the VP, Global Quality Head, responsibilities of the QC Manager will include but are not limited to: • Leading, hiring, developing, training, and evaluating QC personnel, • Devising sound hiring strategies based on business needs, • Supervising and overseeing QC personnel in their roles for safe and efficient verification, approval, release/disposition of HCATS and/or client products/materials, • Delegating responsibilities and supervising the work of laboratory personnel, while providing guidance and motivation to drive maximum performance, • Ensuring and promoting compliance with applicable cGMP and GTP regulations, while ensuring compliance with company and client methodologies, • Assuring alignment and efficient continuity in laboratory practices between sites, • Serving as approver in investigations while overseeing timely closure of deviation reports, change controls, CAPAs, and applicable batch records, • Ensuring completion of all client QC requirements related to GMP cellular products and/or materials, • Overseeing QC role in material dispositions via deviation reporting system, CoAs, and/or client-based systems, if applicable, • Prioritizing, scheduling, and managing multiple projects and resources simultaneously, • Monitoring effectiveness of quality systems, change control activities and their completion, for both, internal and client audit findings, • Evaluating and investigating customer complaints and deviations; coordinating corrective and preventive actions as they relate to the Quality Control function, • Delegating maintenance, tracking, and trending aspects of the deviation reporting system, • Developing and maintaining Key Performance Indicators (KPIs) for laboratory testing, • Interfacing with vendors, suppliers, and in-house production personnel to ensure effective corrective and preventive actions are implemented for recurring product/process discrepancies, when applicable, • Interfacing with management at all levels for alignment on significant deviation resolution and corrective action implementation, • Delegating development, revisions, and implementation of Standard Operating Procedures as related to Quality Control activities, • Participating in and tracking group budget setting and cost containment drives, • Communicating and maintaining trust relationships with senior management, business partners, and clients, • Ensuring company policies and legal guidelines are communicated top-down in the company and that they are followed at all times, • Completing projects and special tasks as assigned by the Global Quality Head, • Off-schedule shifts during weekends and holidays based on business requirements a possibility, • On-call presence preferred while physical personal presence is not possible, • Candidate will oversee QC Scientist and QC Associate I, II, and III roles. The QC Manager will delegate responsibilities to direct reports to achieve the requisite business needs, while providing ongoing support to Manufacturing processes.REQUIREMENTS, • BA/BS/MS in a science or relevant field required, • Master’s in Business Administration or relevant field will be preferred, • 7 – 10 years’ experience in the pharmaceutical, biologics or related industry, • Prior cGMP experience required, • Prior QC laboratory, clinical laboratory, microbiology, hematology, blood banking, or immunology experience in a CGMP/GTP environment a must, • Experience in Flow Cytometry is a must, • 5 + Years experience leading a team is a must. Proven ability to lead, coach, and motivate employees, clearly communicate job requirements and effectively manage performance of assigned staff, • Sound understanding of current Good Manufacturing Practices (cGMPs), • Working knowledge of routine QC laboratory procedures such as flow cytometry and CBC analysis, endotoxin testing, equipment and systems, and understanding of production processes and validation, • Prior experience with reviewing Standard Operating Procedures, work instructions, protocols, methods, method validations preferred, • Proven experience in a supervisory or managerial position, • Demonstrable experience in developing strategic plans based on business needs, • Strong understanding of Quality Control in pharmaceutical/biotechnology/biologics industries, • Thorough knowledge of market changes and forces that influence the company, • Proficient with computer software: Microsoft Office, Visio, • Strong written, oral, and presentational skills, • Strong knowledge of QC Analytical testing methodologies, philosophies, method validation and method transfers, • Strong knowledge of quality systems and ability to interpret Quality standards for implementation and review, • Excellent organizational and leadership skills, • Excellent communication, interpersonal, and presentation skills, • Outstanding analytical and problem-solving abilities, • Strong business acumen, • Ability to think strategically, tactically (detail-oriented), and advise personnel in an effective manner, • 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 responsibilitiesWhile performing the duties of this job, the employee may occasionally be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids and are expected to utilize universal precautions with all human specimens. Other exposures may include gases (nitrogen), or corrosive chemicals (Clorox, potassium hydroxide), or exposure to liquid nitrogen. The noise level in the work environment is moderately noisy. Must have the ability to work in a team-oriented environment and with clientsMust be able to handle the standard/moderate noise of the manufacturing facility Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

As a Senior Data Scientist on the GRI Data Science team, you will partner with our diverse team of Engineers, Economists, Computer Scientists, Mathematicians, Physicists, Statisticians, and Actuaries tasked with mining our industry-leading internal data to develop new analytics capabilities for our

Conduct research, publish and present your findings at relevant scientific venues.

Our data scientists are end-to-end owners. A track record of owning a project end-to-end (from research to production), and partnership with a cross-functional team of data scientists, engineers and product managers to deliver advanced analytics or models. Data scientists at TTD work closely with en

We're expanding our Data & AI team and looking for a senior/lead contributor who's fluent in classical ML and experienced shipping LLM-powered agents into production. Senior/Lead Contributor For Data & Ai Team.

We are looking for a Data Scientist to join SeatGeeks Demand Analytics team, focusing on measurement and optimization of marketing channel performances.

Were looking for a Senior Data Scientist to help design and deploy next-generation agentic AI systems that drive automation, decision?making, and intelligence across large?scale enterprise environments. Mentor & Standardize: Help shape best practices, mentor junior scientists, and contribute to the

Forsyth Barnes is recruiting on behalf of a major retailer for a Senior Data Scientist to strengthen their enterprise data and analytics capability. Collaborate with Lead and Principal Data Scientists to test hypotheses and align models with enterprise strategy.

The R&D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing.

Data scientists at TTD work closely with engineering throughout the lifecycle of the product, from ideation to production and monitoring. Our data scientists are end-to-end owners. A track record of owning a project end-to-end (from research to production), and partnership with a cross-functional te

The R&D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing.

We are hiring a Data Scientist to join our Fraud and Limits team.

The Columbia Nano Initiative (CNI) seeks an outstanding candidate to fill one opening for the position of Senior Director of the CNI Labs at the rank of Research Scientist. The Research Scientist will provide guidance and expertise in various aspects of laboratories operation. The Research Scientist

We are seeking a highly skilled and motivated Senior Data Scientist to join us, working closely with cross-functional teams from product, engineering, marketing and operations to provide data-driven insights and solutions that enhance our products and accelerate growth.

The R&D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing.

As a Senior Applied Scientist on the team, you will lead measurement solutions end-to-end from inception to production. Key job responsibilities - Lead a team of scientists to innovate on state-of-the-art ads measurement solutions leveraging artificial intelligence, causal inference, natural langua

SambaTraveler is seeking an experienced Mammography Technologist for an exciting Travel Allied job in Hackensack, NJ.Shift: 5x8 hr days Start Date: 11/17/2025 Duration: 11 weeks Pay: $2634 / Week.Working in healthcare, your schedule’s always in motion.SambaCare keeps it all on beat.SambaCare maint

Atlas MedStaff is seeking an experienced Mammography Technologist for an exciting Travel Allied job in White Plains, NY.Shift: 5x8 hr PMs Start Date: 11/17/2025 Duration: 13 weeks Pay: $3116.Atlas Medstaff is currently seeking candidates in the Mammo Tech profession for a 13 week contract in the Whi

CrossMed Healthcare is seeking an experienced Mammography Technologist for an exciting Travel Allied job in White Plains, NY.Shift: Inquire Start Date: 11/17/2025 Duration: 13 weeks Pay: $2867.At CrossMed Healthcare Staffing, we aim to create lasting impressions wherever we go.Embark on your healthc

Host Healthcare is seeking an experienced Mammography Technologist for an exciting Travel Allied job in Hackensack, NJ.Shift: Inquire Start Date: 11/17/2025 Duration: 11 weeks Pay: $2625.At Host Healthcare, we are dedicated to empowering the life and healthcare career you deserve.As a nurse, allied,

CrossMed Healthcare is seeking an experienced Cath Lab Tech for an exciting Travel Allied job in White Plains, NY.Shift: Inquire Start Date: ASAP Duration: 13 weeks.At CrossMed Healthcare Staffing, we aim to create lasting impressions wherever we go.Embark on your healthcare traveler journey with us

FlexCare is seeking an experienced Mammography Technologist for an exciting Travel Allied job in White Plains, NY.Shift: 5x8 hr days Start Date: 11/17/2025 Duration: 13 weeks Pay: $3131.Why Clinicians Choose FlexCare.Less hassle, more control: one recruiter, transparent pay, and concierge-level supp

CrossMed Healthcare is seeking an experienced Cath Lab Tech for an exciting Travel Allied job in Paterson, NJ.Shift: Inquire Start Date: ASAP Duration: 13 weeks Pay: $2728 / Week.At CrossMed Healthcare Staffing, we aim to create lasting impressions wherever we go.Embark on your healthcare traveler j

SambaTraveler is seeking an experienced Cath Lab Tech for an exciting Travel Allied job in Pompton Plains, NJ.Shift: 5x8 hr days Start Date: ASAP Duration: 13 weeks Pay: $3121 / Week.Working in healthcare, your schedule’s always in motion.SambaCare keeps it all on beat.SambaCare maintains excellen

CrossMed Healthcare is seeking an experienced Cath Lab Tech for an exciting Travel Allied job in Paramus, NJ.Shift: Inquire Start Date: ASAP Duration: 13 weeks Pay: $2976 / Week.At CrossMed Healthcare Staffing, we aim to create lasting impressions wherever we go.Embark on your healthcare traveler jo

Uniti Med is seeking an experienced Cath Lab Tech for an exciting Travel Allied job in Paterson, NJ.Shift: Inquire Start Date: 12/01/2025 Duration: 13 weeks Pay: $2860 / Week.Uniti Med provides career opportunities to healthcare professionals by aiding medical facilities to fill their staffing needs

Medpro Healthcare Staffing is seeking an experienced Mammography Technologist for an exciting Travel Allied job in White Plains, NY.Shift: 5x8 hr days Start Date: 11/24/2025 Duration: 13 weeks Pay: $3518 / Week.Joint Commission-certified staffing agency, is seeking a quality Mammography Tech for a c

AMN Healthcare Allied is seeking an experienced CT Tech for an exciting Travel Allied job in New York, NY.Shift: 8 hr days Start Date: ASAP Duration: 13 weeks Pay: $3128.Job Description & Requirements.Computed Tomography Technologist - (CT Tech) .StartDate: ASAP Available Shifts: 8 D Pay Rate:

Uniti Med is seeking an experienced Mammography Technologist for an exciting Travel Allied job in White Plains, NY.Shift: Inquire Start Date: 11/17/2025 Duration: 13 weeks Pay: $3250 / Week.Uniti Med provides career opportunities to healthcare professionals by aiding medical facilities to fill their

Fusion Medical Staffing is seeking an experienced Mammography Technologist for an exciting Travel Allied job in White Plains, NY.Shift: Inquire Start Date: 11/17/2025 Duration: 13 weeks Pay: $2976 / Week.Facility in White Plains, New York.Fusion Medical Staffing is seeking a skilled Mammography Tech

Lancesoft is seeking an experienced Mammography Technologist for an exciting Travel Allied job in White Plains, NY.Shift: 5x8 hr days Start Date: 11/17/2025 Duration: 13 weeks Pay: $3551 / Week.LanceSoft’s mission is to establish global cross-culture human connections that further the careers of o

Job Title: GI/Liver Pathologist Job Summary: We are seeking a skilled and highly knowledgeable GI/Liver Pathologist to join our medical team.This role involves examining tissue samples, diagnosing diseases related to the gastrointestinal (GI) system and liver, and providing expert pathology insights

Medical Science Liaison (GI) - Various Locations.A fast-growing, innovation-driven biopharma focused on.Build and maintain relationships with KOLs and clinical sites.Deliver fair-balanced scientific exchange and respond to unsolicited requests.Support clinical trials (site identification, enrollment

The Senior Manager, Oncology, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Senior Manager leads in a matrix environment as part of a cross-functional t

Do you love creating innovative solutions for customers?.AI and Deep Learning and is interested in building data-driven capabilities that drive transformation.As amember of Thomson Reuters Labs you will haveadirect impact on our companybyhelping to create newand innovative capabilities that will del

As a Senior Research Engineer at Delfina, you will work at the intersection of clinical research, product development, and data engineering to design and execute complex data-driven projects that measurably improve pregnancy outcomes and support care providers.

The R&D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing.

Flow Traders is looking for a Senior Research Engineer to join us in our New York office. As a Senior Research Engineer, you will be responsible for helping to lead the development of our trading model research framework and its integration with our platform for deploying/running those models in pro

X-Ray Technologist – Mount Kisco, NY.Optum (formerly CareMount Medical, ProHEALTH New York, Riverside Medical Group).Join Optum in the Tri-State region and be part of a team that’s transforming healthcare.Work with cutting-edge technology and compassionate colleagues who share your passion for h

The R&D Scientist II plays a key role in advancing innovative medical devices based on regenerative technologies. The scientist will work independently on defined projects, contribute to cross-functional teams, and support the smooth transfer of products into manufacturing.

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This is a 3 month contract with possible extension or conversion and a great way to start working with a top-tier healthcare organization!.Possible extension or conversion).Schedule: Mon - Fri 8:00 am - 5:00 pm.Pay Rate is based on experience and educational qualifications.Performs quality X-Ray pro

Swayable is seeking a Senior Engineer blending Python software development expertise with scientific computing, machine learning, and AI experience to advance the state of the art analytics engine that powers our core product. You will work with a talented and diverse team of engineers, data scienti

Flow Traders is looking for a Senior Research Engineer to join us in our New York office. As a Senior Research Engineer, you will be responsible for helping to lead the development of our trading model research framework and its integration with our platform for deploying/running those models in pro

Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is