Medical laboratory technician jobs in Rhode Island

SUMMARY: The Pathology Technologist reports to the Pathology Manager. Under general supervision and within department policies and procedures, performs various complex clinical laboratory tests in one or more of the laboratory sections of the Pathology Department. Work requires a professional level of knowledge in order to read and interpret test results, especially those which are abnormal or atypical. Responsibilities include calibrating instruments, reporting test results, conducting quality controls, and the like. Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another. In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES: Prepares and determines suitable of solutions, reagents and stains following standard laboratory formulas and procedures; may prepare variations of same for special tests.Performs complex clinical laboratory tests in one or more sections of the Pathology Department, which require a professional level of knowledge in order to monitor testing procedures and parameters, and to interpret and analyze test results. Some examples of tests performed include:Performs routine and specialized blood tests to:Type and cross-match blood and assumes responsibility for compatibility between patient and donor.Isolate and identify any unusual or abnormal blood incompatibility factors and Identify atypical conditions in blood specimens.Performs standard hematologic procedures, as well as more specialized and difficult procedures, such as:Identifying and quantifying all formed elements of blood (i.e. platelets, leukocytes, etc.) and Identifying coagulation factors.Isolates microorganisms from a variety of clinical specimens with emphasis on rapid detection of pathogenic organisms using specialized morphological and biochemical methods. Performs antibiotic susceptibility tests.Performs chemical analyses of body fluids in order to determine conditions, such as level of glucose, sodium potassium, chlorides, carbon dioxide, drugs and alcohol in the blood.Records and reviews test results for accuracy and prepares test reports; relay test results and/or reports to physicians or others authorized to receive them.Discusses findings with physicians when necessary.Assists in the instruction of students and residents and in the orientation of new employees to an assigned laboratory section.Performs quality control checks on equipment and reagents, records values and uses results to identify potential problems.Performs new tests and procedures during development stages and makes recommendations for modification and establishment of new tests and procedures.Monitors equipment operation; sets up and calibrates equipment, troubleshoots operational problems and performs preventative maintenance and minor repairs.Logs in specimen and maintains records of specimen during tests; walks to patient floors, draws patient blood samples following established procedures and transports specimens to Pathology for testing.Cleans and maintains laboratory equipment, glassware, instruments, work benches and so forth. MINIMUM QUALIFICATIONS: BASIC KNOWLEDGE:Bachelor's degree in a lab science such as chemical, physical, biological, clinical laboratory science, medical technology or closely related field or equivalent education and experience as defined by CLIA standards.CRENDENTIALS:National certification by ASCP or equivalent in any of the offered categories such as Medical Laboratory Science, Medical Technology, Microbiology, Chemistry, Hematology, or any other recognized categorical certifications.OREligible for national certification with laboratory training including completion of a clinical laboratory training program approved or accredited by the ABHES, NAACLS, or other organization approved by HHSORPreviously qualified or could have qualified as a technologist as defined by CLIA standards for testing personnel.The ability to operate equipment and instruments and to perform all procedures and tests within assigned laboratory section and interpret them accurately.The physical and visual dexterity necessary to conduct and interpret tests.The physical ability to stand and work at laboratory benches.Demonstrated knowledge and skills necessary to provide care patients with consideration of aging processes, human development stages and cultural patterns in each step of the care process.EXPERIENCE:One year experience in a clinical laboratory.WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS:Exposure to odors, infectious materials, toxins and other hazardous substances.Visual strain is encountered while closely examining specimens.Regularly required to stand, lift and carry supplies, etc. Pay Range: * EEO Statement: Brown University Health is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, ethnicity, sexual orientation, ancestry, genetics, gender identity or expression, disability, protected veteran, or marital status. Brown University Health is a VEVRAA Federal Contractor. Location: Rhode Island Hospital - 593 Eddy Street Providence, Rhode Island 02903 Work Type: Work Shift: Day Daily Hours: Driving Required:

We're not just a workplace - we're a Great Place to Work certified employer! Proudly certified as a Great Place to Work, we are dedicated to creating a supportive and inclusive environment. At Sonic Healthcare USA, we emphasize teamwork and innovation. Check out our job openings and advance your career with a company that values its team members! LOCATION: 10 Risho Ave, East Providence, RI 02914 HOURS: 2nd Shift: 3:00pm - 11:30pm; Monday - Friday, w/rotating weekends & holidays FULL TIME: Benefits Eligible ** Shift Differential added to base pay** Why this role matters: Every test you run helps deliver answers that patients and providers rely on. In this role, you won't just perform lab work-you'll be part of a mission to ensure accuracy, reliability, and better outcomes every day. What you'll do: Perform a wide range of waived, moderate, and high-complexity tests with accuracy and confidence Evaluate specimens and apply established criteria to ensure quality results Run quality assurance and control procedures to keep our lab at the highest standards (federal, state, and CAP compliance included) Maintain and calibrate lab equipment so performance is always optimal Document and track results using advanced systems to ensure accuracy and compliance Recognize and troubleshoot control discrepancies, escalating when needed Independently prepare specimens, determine acceptability, and manage storage Follow lab safety procedures while supporting a culture of teamwork and precision What we're looking for: Current certification from ASCP, AMT, or HEW A.S. in Medical Laboratory Technology OR B.S. in Medical Technology, Biological Science, Chemistry, Physical Science, or military equivalent (transcripts required) Strong organizational skills and ability to work independently Clear, professional communication skills with colleagues, physicians, and patients A motivated professional who is excited about career growth and development Bonus points if you bring: 2+ years of hands-on lab experience A knack for problem-solving and continuous improvement We also want you to know: This role will have routine access to Protected Health Information (PHI). Employees will be trained on reasonable safeguards and are expected to maintain strict confidentiality, as well as abide by all applicable privacy and security standards. Employees are expected only to access PHI when it is required to fulfill job duties. Scheduled Weekly Hours: 40 Work Shift: 2nd Shift (United States of America) Job Category: Laboratory Operations Company: East Side Clinical Laboratory, Inc. Per the RIDOH and the RI Governor's recent announcement the new regulation under Rhode Island General Laws § 23- 1-1 and 23-1-17 requires all healthcare workers to be fully vaccinated for Covid-19 by 10/1/2021. ESCL is compliant with this regulation and therefore will require all final candidates for hire to provide a copy of their fully vaccinated status. Sonic Healthcare USA is an equal opportunity employer that celebrates diversity and is committed to an inclusive workplace for all employees. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, age, national origin, disability, genetics, veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

CLICK AND APPLY NOW! Chemistry MT/MLT, Day Shift - Rhode Island - Permanent Hire Day Shift Permanent and full-time position. Chemistry Department. Must be ASCP certified. AS/BS degree required. Reach out to Megan directly at 617-746-2768 (accepts texts) / Megan@ka-recruiting.com. OR schedule a quick call with Megan using this link: calendly.com/megankarecruiting

South County Health is an independent, non-profit healthcare system offering a comprehensive range of advanced inpatient, outpatient and home health services. Accredited by The Joint Commission (TJC), SCH is made up of South County Hospital, South County Home Health, and South County Medical Group. South County Health has received numerous distinctions for patient care and safety, including a 5-star rating on HCAHPS scores, a 5-star rating by CMS for overall hospital quality, and A's for hospital quality and patient safety by The Leapfrog Group. Having celebrated over 100 years of service to southern Rhode Island, South County Health offers an exceptional opportunity to provide our patients with the best care possible while enjoying a healthy work-life balance. Our worksite wellness program was recently recognized as one of the top fifty such programs nationally. We offer competitive salaries and an attractive benefits package which includes, health, dental, vision, tuition reimbursement, 403b, PTO, and a broad range of career development benefits and opportunities. Performs testing, calibration, and quality control for all laboratory tests approved by the Director of the Laboratory according to department policy and procedures. Follows proper procedure for obtaining patient specimens. Identifies and follows through on problems that may adversely effect patient test results. Must have an active ASCP certification as a Medical Technologist, Medical Laboratory Scientist, or Medical Laboratory Technician within one year of hire.

Job Summary: The Medical Lab Technologist II performs routine and special tests according to written protocols to determine test results that will assist in diagnosing and treating patients. This position is generalist position with rotations to Chemistry, Hematology and Blood Bank. Specifications: Bachelors Degree in a biological, chemical, physical or clinical laboratory science from an accredited institution; and Completion of a twelve month clinical laboratory training program approved by the U. S. Department of Education and/or accredited by the National Accrediting Agency for Clinical Laboratory Sciences (NAACLS) or equivalent; and Completion of a nationally recognized certification examination for clinical laboratory scientists, such as that offered by the American Society of Clinical Pathologists (ASCP) or equivalent. Proficiency in the English language required. Care New England Health System (CNE) and its member institutions Butler Hospital, Women & Infants Hospital, Kent Hospital, VNA of Care New England, Integra, The Providence Center, and Care New England Medical Group, and our Wellness Center are trusted organizations fueling the latest advances in medical research, attracting the nation s top specialty-trained doctors, and honing renowned services and innovative programs to engage in the important discussions people need to have about their health. Americans with Disability Act Statement: External and internal applicants, as well as position incumbents who become disabled must be able to perform the essential job-specific functions either unaided or with the assistance of a reasonable accommodation, to be determined by the organization on a case-by-case basis. EEOC Statement: Care New England is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status Ethics Statement: Employee conducts himself/herself consistent with the ethical standards of the organization including, but not limited to hospital policy, mission, vision, and values. WIH Internal Posting Period: 10/15/25-10/24/25

# Summary:#Under the direction of the Laboratory Manager the Cytotechnologist is responsible for the microscopic examination for cytologic diagnosis of GYN and NON-GYN samples.# The Cytotechnologist performs procedures using established and approved protocols requiring the use of good clinical judgment. The cytotechnologist is also responsible in maintaining equipment and records, perform quality assurance activities ensuring test performance, in consultation with the Medical Director. Education: ### Bachelor#s Degree by an accredited school of cytotechnology or equivalent education.# Licensure: None Experience: 3 years# experience in cytotechnology laboratory within the last 10 years is preferred Skills and Abilities: Demonstrates the cognitive abilities necessary to master relevant content in clinical laboratory manuals. Comprehend, analyze, integrate, and synthesize clinical information or data as it relates to laboratory tests and procedures. Utilize reasoning and decision-making skills appropriate to the practice of clinical laboratory science. Has the ability to operate laboratory equipment and adjust instruments to perform laboratory procedures. Is able to use and electronic keyboard to operate laboratory instruments and to calculate, record, evaluate and transmit laboratory information. Has skills in organization and priority setting. Has the ability to work cooperatively with peers and other disciplines. Is able to utilize sound interpersonal skills when interacting with patients and taking into consideration cultural background, linguistic skills and age of customers. Maintains information confidential (HIPAA). Demonstrated customer service skills. Ability to responsive customer service skills when interacting and taking into consideration cultural background, linguistic skills and age of customers. Ability to work cooperatively with peers and other disciplines. Ability to communicate effectively and work collaboratively with peers and other interdisciplinary teams. # Working Conditions, Physical Environment and/or Safety Requirements: Lifting up to 50 lbs. and occasionally lifting and/or carrying such articles as files, books, etc. Hand/eye coordination, physical dexterity and fine motor skills. Has the ability to move freely and safely about the laboratory. Perform moderately taxing continuous physical work, often requiring prolong sitting or standing over several hours. Summary: Under the direction of the Laboratory Manager the Cytotechnologist is responsible for the microscopic examination for cytologic diagnosis of GYN and NON-GYN samples. The Cytotechnologist performs procedures using established and approved protocols requiring the use of good clinical judgment. The cytotechnologist is also responsible in maintaining equipment and records, perform quality assurance activities ensuring test performance, in consultation with the Medical Director. Education: Bachelor's Degree by an accredited school of cytotechnology or equivalent education. Licensure: None Experience: 3 years' experience in cytotechnology laboratory within the last 10 years is preferred Skills and Abilities: * Demonstrates the cognitive abilities necessary to master relevant content in clinical laboratory manuals. * Comprehend, analyze, integrate, and synthesize clinical information or data as it relates to laboratory tests and procedures. * Utilize reasoning and decision-making skills appropriate to the practice of clinical laboratory science. * Has the ability to operate laboratory equipment and adjust instruments to perform laboratory procedures. * Is able to use and electronic keyboard to operate laboratory instruments and to calculate, record, evaluate and transmit laboratory information. * Has skills in organization and priority setting. * Has the ability to work cooperatively with peers and other disciplines. * Is able to utilize sound interpersonal skills when interacting with patients and taking into consideration cultural background, linguistic skills and age of customers. * Maintains information confidential (HIPAA). * Demonstrated customer service skills. * Ability to responsive customer service skills when interacting and taking into consideration cultural background, linguistic skills and age of customers. * Ability to work cooperatively with peers and other disciplines. * Ability to communicate effectively and work collaboratively with peers and other interdisciplinary teams. Working Conditions, Physical Environment and/or Safety Requirements: Lifting up to 50 lbs. and occasionally lifting and/or carrying such articles as files, books, etc. Hand/eye coordination, physical dexterity and fine motor skills. Has the ability to move freely and safely about the laboratory. Perform moderately taxing continuous physical work, often requiring prolong sitting or standing over several hours.

**Lead AI Innovation Lead - Data Science Lab** Guardian is on a transformation journey to evolve into a modern, forward-thinking insurance company committed to enhancing the wellbeing of its customers and their families. As part of the Data & AI team, this role presents a distinctive opportunity to collaborate with the CDAO and the Head of Data Science, actively contributing to Guardian's ongoing evolution. Guardian's Data & AI team spearheads a culture of data insights across Guardian, facilitating the successful realization of our strategic initiatives. Our core activities encompass creating business value from our data and analytic products. Key responsibilities include data lifecycle management, insight development, and data product delivery. We are a team of data analysts, data product owners, data scientists and most importantly, data business leaders. Our solutions and actions are critical to Guardian's revenue growth, risk management and customer experience. Guardian created a Data Science Lab (DSL) to reimagine insurance in light of emerging technology, societal shifts, and evolving consumer needs. The DSL will expedite Guardian's transition to data-driven decision making and insight generation, fostering long-term innovation. The DSL will establish rapid testing capabilities for new technology and the translation of pioneering research into practical, enterprise-wide solutions. In this role as Managing Lead Data Scientist for the DSL, you'll be entrusted with the crucial task of managing the DSL and devising AI strategy for the Data Science team. Your responsibilities will include identifying new AI capabilities, coming up with solutions to scale the Data Science team, leveraging machine learning and artificial intelligence, to drive enterprise-wide innovation across various business lines and Guardian products. You'll collaborate with senior executives on high-impact high-visibility projects to deliver AI/ML solutions that will be market-tested and deployed to make a real difference to risk management and Guardian's overall financial performance. Successful candidates bring expertise in insurance and financial services, a passion for applying cutting-edge ML and AI insights, and the ability to design and implement data science capabilities that foster growth, competitive advantage, and customer satisfaction. **Key Responsibilities Include:** Leadership & Strategy + Lead the Data Science Lab (DSL) by setting strategic direction, driving innovation, and ensuring alignment with Guardian Life's business goals and digital transformation initiatives. + Manage and mentor a high-performing team of data scientists, fostering a culture of continuous learning, experimentation, and excellence. + Monitor developments across the AI and data science community to position Guardian as a leader in responsible and effective AI adoption. + Report and communicate progress, opportunities, and risks to executive stakeholders, delivering insights and recommendations in a clear, actionable manner. Innovation & Research + Stay current with advancements in machine learning (ML), artificial intelligence (AI), and industry trends to identify and evaluate emerging capabilities and technologies. + Collaborate with academic and industry partners to develop and test novel AI/ML methods and approaches. + Introduce and apply ML/AI innovations to practical, high-impact opportunities across Guardian's business units. + Create patentable technologies and methodologies that drive long-term innovation. AI/ML Development + Build and lead experimentation efforts to validate the feasibility and impact of new data science techniques in real-world insurance use cases. + Develop capabilities in Deep Learning, Large Language Models (LLMs), and Generative AI. + Apply AI/ML to unstructured data sources such as insurance contracts, medical records, sales notes, and customer service logs. + Deliver solutions that enhance underwriting risk assessment, claims auto-adjudication, and customer servicing. Operational Excellence + Establish scalable processes, frameworks, and governance models for efficient and responsible AI/ML development, testing, and deployment. + Assess and recommend cutting-edge tools, platforms, and technologies to enhance data science workflows and model lifecycle management. + Actively participate in proof-of-concept evaluations of new data, software, and technologies. Collaboration & Integration + Collaborate cross-functionally with business leaders, technology teams, and data professionals to translate business challenges into AI-driven solutions. + Contribute to the standardization of data science tools, processes, and best practices across the enterprise. + Function as the data science expert in internal and external meetings, including vendor engagements and industry conferences **You are:** + You are passionate about cutting-edge technology and keen on applying new AI/ML algorithms and approaches. + You are analytically driven, intellectually curious, and experienced leading the development and implementation of data and analytic solutions to solve challenging business problems. + You enjoy leading and managing a team of data scientist to crack hard to solve problems with AI/ML and seeing it deployed in-market and generating value for Guardian. You enjoy collaborating with a multi-disciplinary team including data engineers, business analysts, software developers and functional business experts and business leaders. + You have demonstrated track record of managing data science teams and working with business leaders. **You have:** + PhD with 6+ years of experience, Master's degree with 8+ years of experience, or Bachelor's degree with 10+ years of experience in Computer Science, Engineering, Applied mathematics or related field + 7+ years of hands-on ML modeling/development experience + Extensive experience in deep learning models including Large Language Models (LLM) and Natural Language Processing (NLP) + Hands-on experience with GPU, distributed computing and applying parallelism to ML solutions + Strong programming skills in Python including PyTorch and/or Tensorflow + Solid background in algorithms and a range of ML models + Experience leading team of Data Scientist of four or more + Excellent communication skills and ability to work and collaborating cross-functionally with Product, Engineering, and other disciplines at both the leadership and hands-on level + Excellent analytical and problem-solving abilities with superb attention to detail + Proven leadership in providing technical leadership and mentoring to data scientists and strong management skills with ability to monitor/track performance for enterprise success **Location:** + Three days a week at a Guardian office in New York, NY, Holmdel, NJ, Boston, MA, Stamford, CT, Pittsfield, MA or Bethlehem, PA + Remote Candidates who can travel up to 20% of the time to our New York office will be considered. **Salary Range:** $148,940.00 - $244,685.00 The salary range reflected above is a good faith estimate of base pay for the primary location of the position. The salary for this position ultimately will be determined based on the education, experience, knowledge, and abilities of the successful candidate. In addition to salary, this role may also be eligible for annual, sales, or other incentive compensation. **Our Promise** At Guardian, you'll have the support and flexibility to achieve your professional and personal goals. Through skill-building, leadership development and philanthropic opportunities, we provide opportunities to build communities and grow your career, surrounded by diverse colleagues with high ethical standards. **Inspire Well-Being** As part of Guardian's Purpose - to inspire well-being - we are committed to offering contemporary, supportive, flexible, and inclusive benefits and resources to our colleagues. Explore our company benefits at *********************************************** . _Benefits apply to full-time eligible employees. Interns are not eligible for most Company benefits._ **Equal Employment Opportunity** Guardian is an equal opportunity employer. All qualified applicants will be considered for employment without regard to age, race, color, creed, religion, sex, affectional or sexual orientation, national origin, ancestry, marital status, disability, military or veteran status, or any other classification protected by applicable law. **Accommodations** Guardian is committed to providing access, equal opportunity and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. Guardian also provides reasonable accommodations to qualified job applicants (and employees) to accommodate the individual's known limitations related to pregnancy, childbirth, or related medical conditions, unless doing so would create an undue hardship. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact applicant_accommodation@glic.com . **Current Guardian Colleagues: Please apply through the internal Jobs Hub in Workday.** Every day, Guardian helps our 29 million customers realize their dreams through a range of insurance and financial products and services. Our Purpose, to inspire well-being, guides our dedication to the colleagues, consumers, and communities we serve. We know that people count, and we go above and beyond to prepare them for the life they want to live, focusing on their overall well-being - mind, body, and wallet. As one of the largest mutual insurance companies, we put our customers first. Behind every bright future is a GuardianTM. Learn more about Guardian at guardianlife.com .

Certified nursing assistant who has successfully completed a training program approved by the state of Rhode Island for medication administration and whose primary function is to assist in the administering of medications to residents of the assisted living program as ordered by their physician, under the direction of the Director of Nursing Services. The administration of medications shall be in accordance with established nursing standards; the policies, procedures, and practices of this facility, and the requirements of the state. Required Duties Drug Administrative Functions Accurately and safely prepare, administer, and document the oral medications according to physician's order and established policies and procedures of Charlesgate Senior Living Center. Monitor medications to ensure adequate accountability measures are taken when medications are ordered, received into the facility, administered and at narcotic count and change of shift as required by policies and procedures of Charlesgate Senior Living Center and applicable state/federal regulations. Follow the labeling policies and practices of the assisted living program and ensure that all medications administered are properly labeled. Assist with medication charting in accordance with assisted living residence procedures and as directed by the Director of Nursing Services Accurately measure, record, and report the vital signs of residents. Observe and verify that medication is ingested or applied as directed. Document any instance where prescribed medication is not administered, including the reason for refusal Follow the assisted living residences policy and documentation requirements regarding destroying of medications and assist in documenting and removing medications that are discontinued by the physician. Verify the identity of the resident before administering the medication and follow assisted living residence procedures regarding patient self-administration of meds Follow established guidelines concerning the storage of drugs and biologicals Follow established safety precautions in the performance of all duties Ensure that you treat all residents kindly, with dignity, and respect maintaining the confidentiality of all resident care information. General Operations and Other Duties Assist with the daily functions and provisions of assisted living services including dining room and meal service and other duties and functions listed in the certified nurse assistant job description as needed Routinely inspects, cleans and monitors equipment and supplies to ensure resident safety. Reports any equipment or supply issues to the Director of Nursing for correction or repair. Perform other duties as assigned. Must function independently, have flexibility, personal integrity, and the ability to work effectively with residents, personnel, and agencies. Requirements EDUCATION and/or EXPERIENCE Must possess at a minimum a high school equivalency education and additional education to meet the requirements of the state of Rhode Island for licensure as a Certified Nursing Assistant and satisfactorily completed a state approved drug administration program. Must provide documentation of completed education requirements and licensing. COMMUNICATION SKILLS Must be able to read, write, speak, and understand the English language. Must possess the ability to deal tactfully with personnel, residents, family members, visitors, government/agency personnel and the general public. Must be able to relate information verbally or in writing to appropriate supervisory personnel. Be familiar with the meaning and usage of common medical abbreviations, symbols, and terms relative to the administration of medications as used by Charlesgate Senior Living Center, pharmacists, and physicians. Must be able to relate to and work with the ill, disabled, emotionally upset, elderly, and at times hostile people in the facility. REASONING ABILITY Must be able to define problems, collect data, follow detailed instructions, and draw valid conclusions. Must possess the ability to make independent decisions when circumstances warrant such actions. Must also possess the ability to report any issues or problems to appropriate supervisor when warranted. CERTIFICATES, LICENSES, REGISTRATIONS Must have and maintain active appropriate licenses for the administration of duties. Must also attend and participate in provide evidence to Charlesgate of continuing education credits as required by the state to maintain certification. CRIMINAL BACKGROUND Local, state and federal Background Criminal Investigations (BCI checks) must validate no history of criminal activity. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is frequently required to walk, bend, sit, use hands or feet; and talk or hear. The employee is occasionally required to stand and reach with hands and arms. Specific vision abilities required by this job include close vision. Must be able to push, pull, move, and/or lift a minimum of 50 pounds to a minimum height of four feet and be able to push, pull ,move, or carry such weight Exposed to body fluids, infection, odors, and behavior of residents Must be in good general health, meet the general health requirements of the facility including a physical examination, and demonstrate emotional stability in order to cope with the mental and emotional stress of the position Salary Description $21.00/hr

Responsibilities Oversees and leads Donor Testing technical staff and coordinates sample processing, testing, and/or client management. This position may assist with instructional and hands-on training for Donor Testing technical staff and performs CLIA or Non-CLIA competency assessments, as needed. Executes testing and quality control procedures following SOP's as assigned. Testing includes routine donor testing in large batches. Maintains competency in all donor testing functions and follows current Good Manufacturing Processes. Complies with all established policies and procedures including testing and reporting protocols, safety practices, donor and patient confidentiality policies, personnel practices and promotes teamwork and communication both internally and externally. As defined by CLIA/NYSHDOH, this position is responsible for specimen processing (pre-analytic) or testing (analytic), maintaining records of tests and reporting test results in high complexity laboratory. This position performs only those tests that are authorized by the CLIA/NYSDOH laboratory director and performs only those tests that require a degree of skill commensurate with the individual's education, training or experience, and technical abilities. Assists staff to resolve technical problems. Provides technical assistance to internal and external customers for laboratory related issues. Recognizes and reports to supervisor problems encountered during performance of job tasks including equipment malfunction, deviation from standard operating procedure, unusual results, and discrepancy in test controls or controls outside established normal limits. Assists with validations of equipment, test assays and laboratory information systems. Leads and executes quality improvement initiatives to promote continuous process improvements to achieve operational excellence, departmental goals, and organizational goals. Assists with creating and/or revising department regulated documents Positively mentors, coaches, and assists with the training of DT staff, as needed. Participates in ongoing investigational studies Performs required Non-CLIA or CLIA competency assessments for DT staff, as needed. Conducts assessments with appropriate follow-up and recommendations using the competency assessment process/tools. Understands and delivers on customer needs. Utilizes service recovery responses when appropriate. Performs primary and secondary record review of department records Assists with laboratory inventory management processes such as reviewing pre-qualification runs, performing lot changes, and switching out of critical supplies. Promote and contribute to a culture of safety through compliance with all safety SOP's to include wearing proper personal protective equipment (PPE) I.e., safety goggles, gloves, lab coats and proper shoes. Promptly report all safety violation observations and/or safety concerns. Participates in educational activities, leadership training and other corporate initiatives and continuing education to meet national and state regulations. Successful participation in proficiency testing and annual competency assessment programs. Preparing biohazardous waste for shipment Assists with CAPA and root cause investigations Qualifications 4 First Shift - 10 hour shifts per week, every other weekend, holiday rotation Education: Bachelor of Science in chemical, biological, clinical laboratory science or medical technology Related Experience Minimum of four (4) years relevant laboratory experience MT/MLS, or SBB (ASCP) certification Must meet requirements for Testing Personnel for a Highly Complex Laboratory as described in the Clinical Laboratory Improvement Act of 1988 and Supervisor as described in NYSDOH Clinical Laboratory Requirements. The proposed hourly wage is $35.00 to $38.00 Offers made to an individual candidate will depend on a variety of factors, including experience, skills, and job-related education. Overview Founded in 1979, Rhode Island Blood Center (RIBC) has served Rhode Island and the New England area for more than 45 years, delivering more than 90,000 lifesaving blood products annually to 50+ hospitals, EMS and healthcare partners. RIBC is part of New York Blood Center Enterprises (NYBCe), which spans 17+ states and delivers one million blood products to 400+ U.S. hospitals annually. NYBCe additionally delivers cellular therapies, specialty pharmacy, and medical services to 200+ research, academic and biopharmaceutical organizations. NYBCe's Lindsley F. Kimball Research Institute is a leader in hematology and transfusion medicine research, dedicated to the study, prevention, treatment and cure of bloodborne and blood-related diseases. RIBC serves as a vital community lifeline dedicated to helping patients and advancing global public health. To learn more, visit ribc.org. Connect with us on Facebook, X, Instagram, and LinkedIn.

Serco is seeking a SESIF (Submarine EHF SATCOM Integration Facility) Lab technician for their MILSACOM contract supporting NUWCDIVNPT in Newport, RI. You will be part of a small team supporting Code 34 from NUWC. You will be working with other Serco employees and government employees from NUWC. In this role, you will: Provide distance (e.g., telephone, chat, or e-mail) technical assistance in response to Fleet requests received via SubHDR hotline, Information Technology System Management (ITSM) tickets, naval messages (e.g., Casualty Report (CASREP)), or e-mails to resolve terminal, antenna system, and associated baseband equipment hardware, communications planning, software, logistics, documentation, and training issues. The contractor shall submit or update existing ITSM problem report tickets to document issues, recommendations provided, and actions taken to resolve them Operate, troubleshoot, and perform preventative and corrective maintenance on laboratory and facility support equipment. The contractor shall submit ITSM problem reports to document equipment failures or equipment that is not operating per specifications Perform Communications Security (COMSEC) and keymat operations. The contractor shall comply with local NUWCDIVNPT COMSEC policies in the performance of their duties as a COMSEC user. The contractor shall report completion of any COMSEC user tasking to the lab manager (or alternate) via E-mail. The contractor shall immediately report any COMSEC related issues to their Government lab manager or a NUWCDIVNPT COMSEC Account Manager (CAM) if the lab manager is not available Generate NMT images per satellite access authorizations and EHF Service Plans in support of SESIF and Fleet test events Perform laboratory hardware and software configuration control management. Configure lab and applicable equipment to support test events. The contractor shall update and maintain laboratory device records (list or database) per Applicable Documents, and prepare and submit laboratory baseline records to the SESIF Work Center Manager Prepare and submit satellite access requests per Government test requirements, and submit post mission after action reports using Joint Integrated SATCOM Tool (JIST) or equivalent Download and install monthly T-MPSS MPE global scenario updates, and perform data item group imports and exports. The contractor shall document updates in laboratory logbooks Qualifications To be successful in this role, you will have: An active DoD Secret security clearance A High School Diploma and 5 years CSRR/NMT experience OR an Associate's degree and 3 years of CSSR/NMT experience Experience working in a lab environment Ability to work on-site If you are interested in making an impact with a passionate team, submit your application now for immediate consideration. It only takes a few minutes and could change your career! Company Overview Serco Inc. (Serco) is the Americas division of Serco Group, plc. In North America, Serco's 9,000+ employees strive to make an impact every day across 100+ sites in the areas of Defense, Citizen Services, and Transportation. We help our clients deliver vital services more efficiently while increasing the satisfaction of their end customers. Serco serves every branch of the U.S. military, numerous U.S. Federal civilian agencies, the Intelligence Community, the Canadian government, state, provincial and local governments, and commercial clients. While your place may look a little different depending on your role, we know you will find yours here. Wherever you work and whatever you do, we invite you to discover your place in our world. Serco is a place you can count on and where you can make an impact because every contribution matters. To review Serco benefits please visit: ************************************************************ If you require an accommodation with the application process please email: ******************** or call the HR Service Desk at ************, option 1. Please note, due to EEOC/OFCCP compliance, Serco is unable to accept resumes by email. Candidates may be asked to present proof of identify during the selection process. If requested, this will require presentation of a government-issued I.D. (with photo) with name and address that match the information entered on the application. Serco will not take possession of or retain/store the information provided as proof of identity. For more information on how Serco uses your information, please see our Applicant Privacy Policy and Notice. Serco does not accept unsolicited resumes through or from search firms or staffing agencies without being a contracted approved vendor. All unsolicited resumes will be considered the property of Serco and will not be obligated to pay a placement or contract fee. If you are interested in becoming an approved vendor at Serco, please email *********************. Serco is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

Responsibilities: - Responsible for greeting donors at the plasma collection center and conducting a series of registration procedures to verify donor suitability for the plasma pheresis process. - In compliance with Standard Operating Procedures (SOPs), assists qualified donors in completing the screening process. The screening procedures includes but are not limited to: assessing the self-administered health history, answering basic medical questions associated with the donation process, referring donors to medical staff when appropriate and performing health screening procedures such as blood pressure, pulse, weight, temperature. Performs finger stick to obtain sample to obtain donor's hematocrit and total protein levels. - Upon completion of the appropriate training, may educate new donors on the use of therapeutic products made from donated plasma. This includes explaining the screening process, the health screening tests performed, the appointment system, donation fees, center policies, proper nutrition and any other information pertinent to the donor. Ensures that all donor questions are answered timely, accurately and professionally. - May be involved in registering applicant and transfer donors based upon completion of appropriate training and operational needs of the center. - May answer the telephone and answer callers question or transfer call to appropriate staff member. - Maintains alertness and awareness to any reaction by a donor may have during or after the pheresis process and notifies appropriate staff. - Alerts Group Leader or Supervisor of donor flow issues. - Ensures the accurate recording of donor data in the electronic donor information management system as outlined in the SOPs. - Understands the policies and procedures associated with hyper immune programs at the center if applicable. - Maintains clean efficient work environment and ensures sufficient operating supplies and forms are available as needed. Follows all Health Safety & Environmental (HSE) and Occupational Safety and Health Administration (OSHA) policies and procedures. Promotes safety in all actions. - Maintains confidentiality of all personnel, donor and center information. - May be cross-trained in other areas to meet the needs of the business. - Bilingual skills may be required, at the discretion of the organization, to meet the needs of the business. - Perform other job-related duties as assigned. Qualifications: - High school diploma or equivalent required - Minimum of three (3) months experience in a clerical or customer service related position, preferably in medical or health provider environment or equivalent combination of education and experience - Must be able to perform basic math calculations Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable. The expected base pay for this position at hiring is $15.00/hour - $18.35/hour. Please note this wage range reflects what CSL expects to pay for this position at the listed location as of the time of this posting. Individual base pay for a successful candidate within this range is determined by qualifications, skill level, experience, competencies and other relevant factors. **About CSL Plasma** CSL Plasma operates one of the world's largest and most sophisticated plasma collection networks, with over 350 plasma collection centers in the U.S., Europe and China. Headquartered in Boca Raton, Florida, CSL Plasma is a subsidiary of CSL Behring, a global biotherapeutics business and a member of CSL. Plasma collected at CSL Plasma facilities is used by CSL Behring for the sole purpose of manufacturing lifesaving plasma-derived therapies for people in more than 100 countries. The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people. Learn more about CSL Plasma here ************************** and CSL, CSL Behring, CSL Seqirus and CSL Vifor here ******************** . Learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor here at ******************** and CSL Plasma at ************************** . **Our Benefits** For more information on CSL Plasma benefits visit **************************** . **You Belong at CSL** At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more visit ********************careers/inclusion-and-belonging **Equal Opportunity Employer** CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit ********************accessibility-statement . R-262484 CSL makes all employment decisions without regard to race, color, religion, national origin, ancestry, age, sex, gender, pregnancy, disability, marital status, sexual orientation, gender identity, genetic information, military status, protected veteran status (specifically status as a disabled veteran, recently separated veteran, armed forces service medal veteran, or active duty wartime or campaign badge veteran) or other classification protected by applicable US federal, state or local law. CSL complies with all applicable employment laws, including but not limited to Title VII of the Civil Rights Act of 1964, the Americans with Disabilities Act, the Fair Labor Standards Act, and the Immigration Reform and Control Act. ************************************************

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description * Demonstrates and promotes the company vision * Regular attendance and punctuality * Clean, dry, and store glassware for laboratory use * Dispose of waste solutions * Retrieve washroom acids and solvents * Clean and maintain glassware areas * Learn simple laboratory operations such as media production * Learn and use inventory and ordering system for lab supplies * Assist with receiving and placing lab supplies in proper place * Conducts all activities in a safe and efficient manner * Performs other duties as assigned Qualifications * High School Diploma required * Authorization to work in the United States indefinitely without restriction or sponsorship Additional preferences: * Excellent communication (oral and written) and attention to detail * Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude * Ability to learn new techniques, * Perform multiple tasks simultaneously, * Keep accurate records, * Follow instructions and comply with company policies Additional Information Shift: Monday- Friday 12:30pm- 6:30pm Pay Range: $17/Hr.- $20/Hr. * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

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Function All Title All Country/Region All City All State All Zip All Clear Select how often (in days) to receive an alert: Create Alert × Select how often (in days) to receive an alert: Apply now " Title: Lab Technician Location: Providence, RI, US, 02905-5500 Company Name: Univar Solutions USA LLC Requisition ID: 33948 A Place Where People Matter. Start your career journey with Univar Solutions! Here you can make an impact on the world around you and accelerate your career in areas that energize and excite you. Performs a variety of laboratory and research related tasks. Analyzes and tests manufactured and recycled Company products to ensure product quality and composition. What You'll Do: * Uses laboratory equipment to analyze, measure and test chemicals to ensure quality control of products. * Prepares specimens, slides and solutions. * Performs calculations and routine tests. * Prepares and translates Certificates of Analysis and Toxicological reports. * Maintains accurate records. * Stocks laboratory supplies. * Cleans and maintains laboratory equipment. * Adheres to company quality processes, as applicable. * Assists to resolve product quality issues in an efficient and timely manner, as applicable. What You'll Need: * Experienced in laboratory procedures. * Knowledge of laboratory protocols. * Knowledge of cGMP requirements * Experience in SAP preferred Technical Proficiencies Include: * Volumetric analysis (titration techniques) * Operation and maintenance of pH meters * Use of density meters for material characterization * Viscometer operation for viscosity measurements * Spectrophotometric analysis * Karl Fischer titration for moisture determination * Preparation and standardization of chemical solutions * Calibration of laboratory instruments * Standard Operating Procedure (SOP) development and documentation Where you'll work: 6 Harborside Blvd, Providence, RI 02905 Pay & benefits: * The salary range for this position is $49,840.00 - $62,290.00 * The specific salary offered to a candidate may be influenced by a variety of factors including the candidate's relevant experience, education, training, certifications, qualifications, and work location * Available employee benefits include health, vision, dental coverage, along with industry-leading retirement and time off programs What you can expect: * Strong work/life flexibility * To be surrounded by an inclusive team who is collaborative and committed to the achievement of the company * To be rewarded for your contributions with a targeted annual company bonus (if applicable to your role) and annual salary reviews. * Competitive pay and benefits Univar Solutions is a leading, global distributor of chemicals and ingredients essential to the safety, health, and wellbeing of our daily lives from life-saving medicines and vitamins to hand sanitizers and industrial materials used for cleaning, construction, and more. Our global team of more than 9,500 employees support our vision to redefine distribution and be the most valued chemical and ingredient distributor on the planet. We offer a Total Rewards package that includes market aligned pay and incentives as well as a diverse benefits offering to support our employees' physical, emotional, and financial wellbeing. Univar Solutions supports sustainable solutions for the world around us so that we can do our part to help keep our communities healthy, fed, clean, and safe! We are committed to a diverse workforce and a culture of inclusion. Together, we are building a culture that acknowledges the unique experiences, perspectives and expertise of individuals and provides the development and growth opportunities to empower us to redefine our industry. Univar Solutions is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against based on their race, gender, sexual orientation, gender identity, religion, national origin, age, disability, veteran status, or other protected classification. Univar Solutions does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms (collectively Recruiting Firms). Recruiting Firms must enter into a Master Services Agreement (MSA) with Univar Solutions prior to submitting any information relating to a potential candidate. All searches must be initiated by Univar Solutions' Talent Acquisition team and candidates must be submitted via Applicant Tracking System (ATS) by approved vendors who have been expressly requested to make a submission for a specific job opening. No placement fees will be paid to any firm unless the aforementioned conditions have been met. Contacting our hiring managers directly is prohibited. #LI-JM1

Full-time Description Rebuilders Automotive Supply (RAS) is a privately held, family owned, environmentally friendly and service-conscious company serving the automotive aftermarket industry for over 50 years. The RAS team supports three strategic business units: Cores, Catalytic Converters (CAT) and Recall with locations in Coventry, RI and Tampa, Fl. We proudly boast being “green since 1972”. RAS is expanding its lab capabilities! Be part of a growing division using the latest technology in a unique way! The Lab Technician supporting our Catalytic Converter (CAT) Lab is responsible to perform final sample preparation for ICP and XRF testing of catalytic converter substrates in a manufacturing setting including all related equipment, supplies, and materials maintenance. Additionally, the position will record the results and complete the dispositioning of completed samples. The position works closely with the Lab Manager and our operations staff to ensure materials controls and timeliness of lab production. In addition to the below responsibilities this role will perform tasks and activities to support the set-up of the new lab. Prepare sample queue for instrumentation lab through acid digestion and fusion methodologies Execute testing queue and coordinate materials. Compile lab results and issue completed worksheets for final review. Maintain sample integrity. Maintain, calibrate, and run equipment and analytical instruments (i.e. ICP-OES, handheld and tabletop XRF, analytical balances and pan scales, variable micro pipettes, moisture analyzers, fusion ovens, LECO Combustion Instrumentation Perform various daily laboratory maintenance duties including lab waste disposal, glassware & pipette calibration, reagent inventories, etc. Follow written procedures - working towards continuous improvement. Ensure work areas are clean and organized. Track and disposition completed sample inventory. Participate in project work. Requirements In addition to the requirements below, successful candidates will have a a track record of reliable attendance, initiative and a positive attitude! High School diploma or equivalent; Associates degree in chemistry or related, helpful Minimum three years in a related Lab Technician role with experience in wet chemistry techniques, chemical analysis, and data interpretation Knowledge of metallurgy or precious metals extraction helpful Familiar with serial dilution practices to prepare standards, mobile phases, and reagents Experience in the operation, calibration, and maintenance of analytical instruments (knowledge of ICP-OES, XRF and Combustion Methodologies helpful) Experience in an industrial lab environment; high level of awareness of safety protocols and best practices Demonstrated ability to learn and perform new lab specific analytical methods. Familiar with quality system of controls for laboratories to ensure the uniformity, consistency, reliability, reproducibility, quality, and integrity of processes. Proficient IT system knowledge: Excel (data entry, data analysis, report generation) Lab Management system experience preferred. Competencies: Attention to detail: ability to pay close attention to details and follow precise procedures to ensure accurate results Analytical and problem-solving skills: ability to analyze data and identify any anomalies; strong problem-solving skills to troubleshoot and find solutions to any problems that arise. Organizational skills: responsible for managing multiple experiments simultaneously; ability to track all the details, including samples, chemicals, and instruments. Communication skills: ability to communicate effectively with team, both verbally and in writing RAS offers a competitive salary and comprehensive benefits package. Medical, Dental and Vision FSA and HRA (Health Reimbursement Account) Life and AD+D Voluntary supplemental insurance (Life, AD+D, LTD, and Critical Illness) PTO and Paid Holiday's 401k w/match Tuition Reimbursement This is a non-exempt, hourly position. Pay range $18.00/hr - $27.00/hr Hours: Monday - Friday, 7:00am - 3:30pm Must be able to pass a post offer background check.

2nd shift Lab Tech II - Analytical Services Job Title: Analytical Services Lab Technician II Department: Analytical Services Lab Reports to: Quality Mgr Job Function: Perform chemical analysis on raw materials, in-process materials, finished soap bars or specialty chemicals using instrumentation and/or wet chemical methods. Perform routine and non-routine analysis under the supervision of the Analytical Services Team leader. Duties and Responsibilities: 1. Analyze materials using standard wet chemical techniques that include, but not limited to, titrations (colorimetric/potentiometric end points), gravimetric methods, specific gravity, and water content by Karl Fisher or Xylol method. 2. Produce and maintain analysis records, laboratory reports and C of A's 3. Provide analytical data to production and make basic recommendations on batch corrections when required. 4. Maintain sample retains of raw materials and finished goods. 5. Practice good laboratory practices (GLP) in all laboratory operations. 6. Comply with the Chemical Hygiene Plan and Environmental policies when handling and disposing of chemicals. 7. Perform additional duties as requested by those authorized to request such activities. 8. Assure that all Lab areas are kept well stocked, clean and orderly. Assist in developing new product stability studies, testing plans and result archival. Minimum Knowledge, Skills and Abilities: 1. The Technician I will have a High School Diploma (or GED) or higher degree in a science with 0-1 years of laboratory experience. 2. The technician should have a basic knowledge of software for word processing & spreadsheets and be able to learn the use of company specific software. 3. The technician should be proficient in English (both written and oral form). 4. Toe technician should have basic math skills 5. The technician should be willing to learn basic laboratory techniques. 6. The technician should be able to communicate well with colleagues and be able to work well with other members of the Analytical Services lab team Working Conditions and Physical Demands: 1. Ability to lift up to 40 pounds. 2. Ability to work in a fast-paced environment. 3. Ability to work with hazardous materials when provided required PPE

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Essential Duties and Responsibilities: Demonstrates and promotes the company vision Regular attendance and punctuality Reads, understands and follows management system requirements as relevant to responsibilities, including but not limited to requirements found in the Quality Manual, SOPs, Local Work Instructions and Methods which in turn ensures compliance with ISO/IEC 17025/AOAC ALACC requirements and relevant government regulatory. Adhere to all health, safety, and environmental regulations relative to assigned analytical work; maintain and assist others in maintaining a clean, safe work environment. Registration of incoming samples (as needed), maintaining a neat and accurate record system of work performed on a daily basis and as needed for quality control tests or regulatory purposes. Enter the sample data into Eurofins eLIMS system in a timely and accurate manner. Complete laboratory testing on all incoming samples in an accurate, efficient and timely manner; ensure sample turnaround time goals are met or exceeded. Verify results and submit results to the appropriate personnel for transmission, in a timely manner. Identify process difficulties and report these together with proposed solutions to supervisor. Maintain a perpetual state of readiness and willingness to respond to the queries and needs of clients, staff, and co-workers. Maintain cooperative working relationships with all company employees. Communicate orally and in writing to co-workers. This includes “intra” and “inter” departmental employees. Promote the company image through the exercising of sound and ethical business practices as related to the public and our customers. Continually strive to improve the quality of work we provide to our clients through existing and new technologies Identify non-conformances and out-of-specifications Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Education/Experience: HS Diploma and 1-2 years' laboratory experience required. Additional preferences: BS Degree in Microbiology, Food Sciences, Chemistry, Biology, Biochemistry or a related field Proficient in plate reading Proficient in food pathogen detection platforms (BAX, MDS, VIDAS or similar systems) Some knowledge of food pathogen confirmation procedures Additional Information Shift: Monday- Friday 12:30pm- 6:30pm Pay Range: $21/Hr.- $27/Hr. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

2nd shift Lab Tech II - Analytical Services Job Title: Analytical Services Lab Technician II Department: Analytical Services Lab Reports to: Quality Mgr Job Function: Perform chemical analysis on raw materials, in-process materials, finished soap bars or specialty chemicals using instrumentation and/or wet chemical methods. Perform routine and non-routine analysis under the supervision of the Analytical Services Team leader. Duties and Responsibilities: 1. Analyze materials using standard wet chemical techniques that include, but not limited to, titrations (colorimetric/potentiometric end points), gravimetric methods, specific gravity, and water content by Karl Fisher or Xylol method. 2. Produce and maintain analysis records, laboratory reports and C of A's 3. Provide analytical data to production and make basic recommendations on batch corrections when required. 4. Maintain sample retains of raw materials and finished goods. 5. Practice good laboratory practices (GLP) in all laboratory operations. 6. Comply with the Chemical Hygiene Plan and Environmental policies when handling and disposing of chemicals. 7. Perform additional duties as requested by those authorized to request such activities. 8. Assure that all Lab areas are kept well stocked, clean and orderly. Assist in developing new product stability studies, testing plans and result archival. Minimum Knowledge, Skills and Abilities: 1. The Technician I will have a High School Diploma (or GED) or higher degree in a science with 0-1 years of laboratory experience. 2. The technician should have a basic knowledge of software for word processing & spreadsheets and be able to learn the use of company specific software. 3. The technician should be proficient in English (both written and oral form). 4. Toe technician should have basic math skills 5. The technician should be willing to learn basic laboratory techniques. 6. The technician should be able to communicate well with colleagues and be able to work well with other members of the Analytical Services lab team Working Conditions and Physical Demands: 1. Ability to lift up to 40 pounds. 2. Ability to work in a fast-paced environment. 3. Ability to work with hazardous materials when provided required PPE

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Demonstrates and promotes the company vision Regular attendance and punctuality Clean, dry, and store glassware for laboratory use Dispose of waste solutions Retrieve washroom acids and solvents Clean and maintain glassware areas Learn simple laboratory operations such as media production Learn and use inventory and ordering system for lab supplies Assist with receiving and placing lab supplies in proper place Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications High School Diploma required Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Shift: Monday- Friday 12:30pm- 6:30pm Pay Range: $19/Hr.- $23/Hr. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Employment Type: Contract Business Unit: Commercial AS ARI Duration: 18+ months (with likely extensions and/or conversion to permanent) Notes: $18.00/hour 3 Key Consulting is hiring an Associate Laboratory Support for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: As the candidate for this largely laboratory-based position, you will be responsible for analytical support and technology development impacting process and product development teams. You will work cross-functionally and across Process Development sites as you use analytical science to help drive efficient development and scalable understanding of processes and products. Why is the Position Open? Supplement additional workload on team. Top Must Have Skills: Science related degree Great Communication skills Familiarity with basic analytical lab equipment Excellent interpersonal skills Day to Day Responsibilities: Buffer and mobile phase preparation pH meter calibration Balance calibration Sample receiving Lab organization as needed Basic Qualifications: Bachelors degree in Analytical Chemistry, Physical, Life Sciences or related technical discipline. Min 0-2 years' experience performing analytical testing. Understanding, research in, and hands-on experience in protein analysis in support of process development/scale up activities and formulation development in GMP and non-GMP environments Experience with analytical lab equipment including pH meters, lab scales, pipettes. Generate complete, accurate, and concise documentation using electronic systems and electronic laboratory notebook. High energy individual who can multi-task and handle a fast-pace, dynamic work environment. Operate specialized laboratory equipment and instrumentation. Perform general laboratory housekeeping activities including buffer preparation, ordering chemicals and consumables, receiving samples. Complete training on assigned tasks. Comply with safety guidelines and site specific procedures which include but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books. Employee Value Proposition: To work with a dynamic team and gain additional experience. Interview process: Video Skype Panel Interview We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team