Laboratory technician jobs in Rhode Island

Job Description**Please note the schedule for this role is Mon-Fri 2:30pm-12:00am and Saturdays as needed.** The FSQA Tech IV is a senior-level technician responsible for ensuring compliance with all food safety and quality standards across production shifts. This role supports the FSQA Supervisor and Manager in executing HACCP, GMP, and SQF protocols, conducting inspections, and mentoring junior technicians. Tech IV plays a critical role in maintaining regulatory compliance and driving continuous improvement in food safety performance. Duties/Responsibilities: Conduct and document routine inspections of raw materials, in-process products, and finished goods. Perform environmental monitoring, allergen testing, and sanitation validations. Lead pre-operational inspections and verify corrective actions. Support internal and third-party audits by preparing documentation and participating in walkthroughs. Train and mentor FSQA Tech I-III team members on SOPs, GMPs, and food safety protocols. Monitor and enforce compliance with HACCP, USDA, FDA, and company-specific standards. Investigate and document deviations, non-conformances, and customer complaints. Collaborate with production, sanitation, and maintenance teams to resolve quality issues. Maintain accurate records in compliance with SQF Edition 9 and internal traceability systems. Participate in BOS (Behavior Observation Surveys), Risk Prediction assessments, and 5S audits. Required Skills/Abilities: Strong understanding of food safety regulations and quality assurance principles. Excellent verbal and written communication skills. Ability to interpret and apply regulatory standards (USDA, FDA, SQF, HACCP). Proficient in Microsoft Office Suite and quality management software. Strong attention to detail and organizational skills. Ability to lead by example and coach others in a team environment. Capable of working independently and managing multiple priorities under pressure. Comfortable working in cold, wet, or noisy production environments. Education and Experience: High school diploma or GED required. Associate or bachelor's degree in Food Science, Microbiology, Biology, or a related field preferred. HACCP certification and SQF practitioner training preferred. Minimum 3-5 years of experience in food safety or quality assurance in a USDA-regulated facility. Demonstrated experience with HACCP, GMP, and SQF systems. Experience leading audits and mentoring junior team members is highly desirable. Familiarity with digital quality systems (e.g., Redzone, TraceGains) is a plus. Working Conditions: This position requires standing, walking, and working in cold, wet, or noisy environments. Must be available for rotating shifts, weekends, and holidays as needed. this pay rate includes a 2nd shift pay differential We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

NEW Microbiology/Molecular Technologist Opening at a full service clinical laboratory in Rhode Island! This laboratory is fully accredited by CAP and CLIA. They are looking to hire a permanent and full time Microbiology/Molecular Technologist on evening shift! This laboratory offers a culture where there are ample opportunities for challenge, growth and recognition! For consideration, applicants must have either a Bachelor's Degree in Medical Technology/MLS and/or an AS Degree in Medical Laboratory Science/Medical Laboratory Technician AND ASCP Certification as a Medical Technologist (MT or MLS or MLT) or Microbiology Technologist (M). This position is Monday through Friday. New graduates and experienced candidates are both encouraged to apply! Local applicants are preferred! This laboratory is offering a highly competitive hourly rate and a top notch benefits package! Benefits include medical, dental, vision, prescription drug, generous PTO, life insurance, FSA, 401K and more! Interested in learning more? Contact Andrea at andrea@ka-recruiting.com or call/text 617-746-2745! ACC 253311740

Department Research & Development Employment Type Full Time Location North Kingstown, RI Workplace type Onsite Compensation $27.00 - $32.00 / hour Reporting To Tony Franco How You Will Help What You Will Have About ASC Engineered Solutions Following the 2019 merger of Anvil International and Smith-Cooper International, the unified company relaunched in March 2021 as ASC Engineered Solutions. Under a single name and logo, ASC Engineered Solutions continues our focus on improving the customer experience every day and striving to deliver service excellence. The evolved ASC Engineered Solutions brand reinforces a focus on what matters most to customers: quality. As a solutions provider, this quality is reflected in our precision-engineered products, support and knowledge. Our organization is a dependable strategic partner focused on its customers' success.

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. Pay Transparency Our Total Rewards package includes competitive pay, performance-based incentives, and benefits that promote well-being and work-life balance-so you can thrive both professionally and personally. Eligible employees also gain access to a wide range of benefits from comprehensive health coverage and health savings accounts to retirement plans, life and disability insurance, and time-off programs that support work-life balance. Program availability may vary based on factors such as contract type, location, hire date, and applicable collective bargaining agreements. Salary range: The range for this position can be found at the top of the posting. This range is provided as a general guideline and represents a good faith estimate across all experience levels. Actual base salary will be determined by a variety of factors, including but not limited to, the scope of the role, relevant experience, job-related knowledge, education and training, key skills, and geographic market considerations. For roles available in multiple states, the range may vary to reflect differences in local labor markets. In addition to base salary, eligible positions may include other forms of compensation such as annual bonuses or long-term incentive opportunities. Benefits HIGHLIGHTS - Comprehensible Benefits for Full-time Employees (Part-time members receive a customized package tailored to their role). Medical, dental, and vision insurance Robust vacation and sick leave benefits, and flexible work arrangements where permitted by role or contract 401(k) plan that includes employer matching funds Tuition reimbursement program Life insurance and disability coverage Optional coverages you can buy, including pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection Birth, adoption, parental leave benefits Employee Assistance Plan that includes counseling conditions Specific benefits are dependent upon the specific contract as well as whether the position is covered by a collective bargaining agreement or the Service Contract Act. To review all Serco benefits please visit: ****************************************** Serco complies with all applicable state and local leave laws, including providing time off under the Colorado Healthy Families and Workplaces Act for eligible Colorado residents, in alignment with our policies and benefit plans. The application window for this position is for no more than 60 days. We encourage candidates to apply promptly after the posting date, as the position may close earlier if filled or if the application volume exceeds expectations. Please submit applications exclusively through Serco's external (or internal) career site. This is a U.S.-based role. If an applicant has any concerns with job posting compliance, please send an email to: ********************.

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

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.

Prysmian is the world leader in the energy and telecom cable systems industry. Each year, the company manufactures thousands of miles of underground and submarine cables and systems for power transmission and distribution, as well as medium low voltage cables for the construction and infrastructure sectors. We also produce a comprehensive range of optical fibers, copper cables and connectivity for voice, video and data transmission for the telecommunication sector. We are 30,000 employees, across 50+ countries. Everyone at Prysmian has the potential to make their mark; because whatever you do, wherever you are based, you will be part of a company that is helping transform the world around us. Make Your Mark at Prysmian Group - Join Us Overview: Provide technical support for all aspects of wire and cable design and development including product design, material selection & testing, performance testing & improvements, manufacturability, feasibility, quoting activities, productivity enhancements, manufacturing process & equipment changes, new design changes, and existing product design changes. Proficient in laboratory equipment functions, test procedures, and interpretation of internal & external product specifications. Research, source, evaluate, develop, change, or improve as necessary all polymers and compound formulations to comply with product specifications. Principal Duties/Responsibilities/Qualifications: Responsible for understanding and performing all tasks and responsibilities according to Job Safety Practices (JSP) or other internal or external safety policies and regulatory standards such as OSHA and NFPA. Responsible for safety and housekeeping procedures and for maintaining a safe and clean work environment. Responsible for adhering to all health, safety, and environmental policies and regulations. Develop/create/modify/maintain new and existing compound formulations to satisfy customer requirements, new product development specifications, or cost savings initiatives. Develop and/or modify existing material formulations to achieve annual product cost reductions. Communicate with material suppliers to initiate supplier new product development and cost savings projects; establish list of alternate ingredients; maintain material recipes and mixing process parameters. Identifies, documents, and verifies processing requirements for new materials. Develops necessary documentation for new programs. Investigates, and identifies DTC savings related to materials and/or design of the components used to manufacture products. Prepares and presents technical information and presentations for internal or external customers and management Supports sales and marketing team with technical discussion and documentation. Communicates with Global R&D team to learn and transfer knowledge. Maintains current knowledge of latest material technology for wire and cable products for potential implementation. Identifies, develops, and integrates strategies to minimize the organizations environmental impact. Promote sustainable policies and practices and develops applications such as less scrap, more environmentally friendly compound recipes and ingredients, better reclaimable or recyclable products, increase water conservation, lower electric & fuel energy consumption, etc. Qualifications: Able to develop and execute a plan as a team leader or team participant. Highly developed team skills, both as a team member and leader Ability to multi-task and manage competing priorities. Good verbal and written communication skills Strong team player Demonstrated ability and initiative to drive change Strong quantitative, analytical, and problem-solving skills Able to learn new ideas, concepts and skills quickly and effectively Knowledgeable and audit compliant to the following processes and systems. ISO9001 Quality management system ISO14001 Environmental management system IAFT16949 Automotive quality management system APQP (Advanced Product Quality Planning DFMEA, PFMEA, FMEA (Design/Potential Failure Mode & Effects Analysis) PPAP (Production Part Approval Process) IMDS (International Material Data System) Education Bachelor of Science Undergraduate Degree in Chemical Engineering, Polymer Science, Chemistry, or related field. One to three years of experience is desired. Work Environment/Physical Demands: Corrected vision to 20/20 being able to clearly see objects at long or short distances and be able to see details in small objects and read fine print Able to visually distinguish colors accurately Occasional manual lifting to 50 pounds Frequent manually push/pull, scoot, slide, rotate or roll product or objects that are medium to large size and of various weights short distances usually on flat surfaces but occasionally on sloped surfaces, in order to place or reposition product or objects. Able to lift and carry by hand various tools, materials, containers usually small to moderate in size Comply with all PPE(Personal Protective Equipment) requirements for job duties and tasks Prysmian, as an Equal Opportunity Employer, aims to attract and recruit individuals with diverse backgrounds, skills, and abilities. We strongly believe that diversity brings significant value at all levels of the organization, increasing the possibility of capturing market opportunities and maximizing value for our customers and stakeholders. With Diversity, Equity, and Inclusion (DE&I) as part of our Social Ambition 2030 and a strategic pillar of our Company culture, Prysmian is committed to the development of an organization that prioritizes talent, where people feel respected, included, and free to fully express their potential just as they are. All Managers and HRs in Prysmian are responsible for ensuring DE&I policies are respected during the recruiting process, as well as recognizing and mitigating unconscious biases that must not influence our selection processes. All persons will be considered for employment without regard to their race, ethnicity, religion, nationality, origin, citizenship status, socio-economic status, age, sex, gender identity or expression, sexual orientation, marital status, disability, military service or veteran status, pregnancy, parental leave, medical conditions, or any other characteristic protected by applicable federal, state or local laws. Prysmian will endeavor to make a reasonable accommodation for any disclosed physical or neurological condition or disability of a qualified applicant unless the accommodation would impose an undue hardship on the operation of our business. Visit our DE&I Page to learn more about Prysmian's commitments. Your application data will be treated according to our Data Protection Policy. If you believe you require assistance to complete this form or to participate in an interview, please contact us at *********************************. ************************************************************************************ ******************************************************************************************************* ********************************************************************************************

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.

The Quality Assurance Representative is responsible for performing detailed quality checks on all equipment being shipped from the Rhode Island Warehouse. This role ensures accuracy in documentation, labeling, and compliance with operational standards, reducing errors and improving customer satisfaction. Duties and Responsibilities: * Perform QC checks on all orders to be shipped verify accuracy and functionality. * Ensure compliance with standardized procedures. * Collaborate with configuration technicians and fulfillment teams to resolve discrepancies. * Maintain QC records and contribute to process improvement initiatives. * Analyze trending quality issues conduct root cause analysis to be able to reduce the frequency of errors Required Qualifications: * High school diploma or equivalent * Strong attention to detail and ability to follow standardized procedures. * Entry-level experience with basic computer systems, ticketing tools, and documentation platforms * Ability to prioritize and manage multiple tasks in a fast-paced environment * Strong communication and teamwork skills * Ability to lift and move equipment as needed Preferred Qualifications: * Associate's degree, technical certification, or equivalent experience. * Familiarity with Network equipment and other communications hardware. * Proven experience in analytical process improvement, including identifying inefficiencies, implementing corrective actions, and documenting results. * Working knowledge of internal ticketing and order management systems. * Strong problem-solving skills and ability to adapt to shifting priorities. * Prior experience in a fast-paced lab, logistics, or telecom environment. Granite delivers advanced communications and technology solutions to businesses and government agencies throughout the United States and Canada. We provide exceptional customized service with an emphasis on reliability and outstanding customer support and our customers include over 85 of the Fortune 100. Granite has over $1.85 Billion in revenue with more than 2,100 employees and is headquartered in Quincy, MA. Our mission is to be the leading telecommunications company wherever we offer services as well as provide an environment where the value of each individual is recognized and where each person has the opportunity to further their growth and achieve success. Granite has been recognized by the Boston Business Journal as one of the "Healthiest Companies" in Massachusetts for the past 15 consecutive years. Our offices have onsite fully equipped state of the art gyms for employees at zero cost. Granite's philanthropy is unparalleled with over $300 million in donations to organizations such as Dana Farber Cancer Institute, The ALS Foundation and the Alzheimer's Association to name a few. We have been consistently rated a "Fastest Growing Company" by Inc. Magazine. Granite was named to Forbes List of America's Best Employers 2022, 2023 and 2024. Granite was recently named One of Forbes Best Employers for Diversity. Our company's insurance package includes health, dental, vision, life, disability coverage, 401K retirement with company match, childcare benefits, tuition assistance, and more. If you are a highly motivated individual who wants to grow your career with a fast paced and progressive company, Granite has countless opportunities for you. EOE/M/F/Vets/Disabled

Summary: Under the direction of the Central Processing Supervisor the Laboratory Assistant performs all work station function in Central Processing area of the Laboratory including electronic patient registration and test ordering, processing of laboratory specimens for analysis, electronic ordering and packaging of specimens referred to a reference laboratory for analysis, specimen handling and planting of microbiology specimens, processing of specimens for cytologic and pathologic examination. Performs the duties of a Client Services Representative when needed. # Education: High School diploma or equivalent. # Experience: Medical terminology and computer skills required. Previous laboratory experience preferred # Skills # Abilities:###### ########################################################### Working knowledge of laboratory terminology and specimen handling Ability to utilize sound interpersonal skills when interacting and taking into consideration cultural background, linguistic skills and age of customers. Computer skills Ability to work cooperatively with peers and other disciplines Ability to read and interpret data, reports, reading material Ability to respond to incoming calls, transcribe details and accurate messages Ability to file data/reports utilizing system design Maintains information confidential (HIPAA) Demonstrated customer service skills Ability to utilize 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 Summary: Under the direction of the Central Processing Supervisor the Laboratory Assistant performs all work station function in Central Processing area of the Laboratory including electronic patient registration and test ordering, processing of laboratory specimens for analysis, electronic ordering and packaging of specimens referred to a reference laboratory for analysis, specimen handling and planting of microbiology specimens, processing of specimens for cytologic and pathologic examination. Performs the duties of a Client Services Representative when needed. Education: High School diploma or equivalent. Experience: Medical terminology and computer skills required. Previous laboratory experience preferred Skills & Abilities: * Working knowledge of laboratory terminology and specimen handling * Ability to utilize sound interpersonal skills when interacting and taking into consideration cultural background, linguistic skills and age of customers. * Computer skills * Ability to work cooperatively with peers and other disciplines * Ability to read and interpret data, reports, reading material * Ability to respond to incoming calls, transcribe details and accurate messages * Ability to file data/reports utilizing system design * Maintains information confidential (HIPAA) * Demonstrated customer service skills * Ability to utilize 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

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: East Providence, RI HOURS: 40/week FULL TIME: Benefits Eligible In this role you will: Direct and control the operations of the Microbiology and the Molecular laboratory including overseeing testing, instrumentation maintenance, staff training, competency assessment, proficiency evaluation, performance management and documentation Develop, engage, recognize and support technical and non-technical staff Manage department and individual performance by providing feedback and coaching to staff members Maintain departmental operating policies and procedures to include departmental programs, quality control, quality assurance and safety Review completion of patient test results, quality control results and tracks productivity Take corrective action to resolve issues involving test results, quality, instrumentation, compliance and employee performance Provide technical training to staff All you need is: BS Degree in Medical Technology, Clinical Laboratory Science, Biology, Chemistry or Physical Science Certified MT or MLT from American Society of Clinical Pathologists (ASCP) Minimum 4 years of (Micro) bench tech experience, required Superior communication and interpersonal skills Excellent organizational skills Ability to promote teamwork in a positive work environment Scheduled Weekly Hours: 40 Work Shift: Job Category: Laboratory Operations Company: East Side Clinical Laboratory, Inc. 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.

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

Located in Bristol, Rhode Island for 50 years, Tri-Mack is a leading manufacturer of high-temperature thermoplastic components for the aerospace-defense, semiconductor, energy and medical industries. Our broad capabilities include collaborative engineering, tool making, injection molding, thermoplastic composite processing, multi-axis CNC machining, bonding and assembly, testing and quality control - all within a modern, environmentally controlled 60,000 sq. ft. facility. Our culture is based on values that promote respect, teamwork and accountability and we are committed to meeting customer requirements through our ISO 9001/AS9100 quality management system. PLEASE NOTE - Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time Position: Quality Control Technician The Quality Control Technician / Vision System Programmer is responsible for the programming of vision measuring systems, developing quality control plans and inspection records for precision machined and assembled parts. It requires good working knowledge of standard precision measurement tools such as micrometer, calipers, height gages, and optical comparator, as well as familiarity with the vision system inspection of parts in order to verify conformance to specifications. The role is to detect and contain quality issues in order to ensure compliance or report non-conforming parts/procedures, as well as to correct and prevent them. Responsibilities & Accountabilities: Program vision measuring systems Perform inspections across various stages of production, verifying conformance to prints and specifications. Investigate product quality issues and determine root cause and corrective actions Perform first piece inspection and final inspection. Assist with both internal and external audits. Work with Engineering and Production to address any product issues. Conduct yourself in an ethical and professional manner and always follow Tri-Mack Values: Respect, Teamwork, Integrity, Accountability and Durability Adhere to all AS9100 requirements as specified in work instructions and by your supervisor. All other duties assigned. Education, Skills & Experience: High School diploma required. Some college-level coursework preferred. 2+ years working in a manufacturing Quality Control environment. Familiarity with using and programming of vision measuring systems. Experience with manual micrometers, calipers and optical comparators. Experience with engineering blueprint reading Demonstrated written and oral communication skills Ability to analyze and prioritize information. Must be able to work independently. Use of computers and Microsoft Word, Excel and Outlook. Our Benefits: We offer competitive salaries and generous benefits, including: 40 hour week - Monday-Friday, overtime available Generous Medical, Life, Dental and Vision Insurance programs Paid Time Off, Paid Holidays, Sick & Safe Leave 401(k) with Company Match Tuition Reimbursement If you are looking for an innovative, values-driven company where you can put your aptitude and expertise in quality control to work, grow your career and take on ever-bigger challenges, you may just have found the place! We know our continued success is dependent upon our employees, which is why we are always on the lookout for reliable, knowledgeable and dynamic individuals with past success in a collaborative team setting, working with clear objectives and direction. *Tri-Mack Plastics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status or genetic information. Tri-Mack is a drug-free work environment. Pre-employment drug screening (excludes THC) and background checks are required.

Tremco Construction Products Group brings together Tremco CPG Inc.'s Commercial Sealants & Waterproofing and Roofing & Building Maintenance divisions; Tremco Barrier Solutions Inc.; Dryvit, Nudura, and Willseal brands; Prebuck LLC; Weatherproofing Technologies, Inc.; Weatherproofing Technologies Canada and PureAir Control Services, Inc. Altogether, Tremco CPG companies operate 21 manufacturing facilities, 6 distribution sites, and 3 R&D/ R&D/technology sites, and employ more than 2,700 people across North America. GENERAL PURPOSE OF THE JOB: Performs visual and physical inspection, sampling, testing, and control of parts, products, and raw materials to conform to established specifications, applicable standards, and the ISO 9001 Quality System. ESSENTIAL DUTIES AND RESPONSIBILITIES: Follows the established quality control procedures to ensure all products are manufactured in compliance with IMS, customer specifications, ISO9001:2015, and ISO14000-2015. Conducts the inspection and testing of raw materials and products, both in process and finished. Performs color quality control and corrections by interpreting results obtained using appropriate measurements. Inspects, calibrates, and supervises the use of various instrumentation for testing. Performs data analysis and provides feedback and improvement suggestions to plant personnel, production management, QC Supervisor, and Quality Assurance Manager on all issues concerning quality. Maintains Quality Control documents and daily reporting of information. Assists in complaint investigations by performing tests to detect or duplicate issues observed in the field. Assists in troubleshooting machine functions and production issues as they arise. Maintains a clean and organized work area. Performs other duties as assigned. EDUCATION REQUIREMENT: High school diploma or general education degree (GED). EXPERIENCE REQUIREMENT: A minimum of 1-2 years of experience in a quality control role within a manufacturing environment with oversight of both raw materials and finished goods. OTHER SKILLS, ABILITIES, AND QUALIFICATIONS: Microsoft Office Suite. Previous experience using enterprise software such as SPA is preferred. PHYSICAL DEMANDS: Incumbent must be able to stand, walk, sit, use hands, reach, climb, balance, kneel, talk, hear, and lift up to 50 lbs. BENEFITS AND COMPENSATION: The hourly rate for applicants in this position generally ranges between $19.57 and $23.00. This range is an estimate, based on potential employee qualifications, operations, needs, and other considerations permitted by law. The Company offers a variety of benefits to its employees, including but not limited to health insurance, paid holidays, paid time off, 401(k) Savings and Trust & Plan with company match, Company Pension Plan, Performance-Based Bonus/Commission, and continuing education. All qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

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 This position is not available for immediate hire. Shift: Monday- Friday 12:30pm- 6:30pm Pay Range: $21/Hr.- $27/Hr. 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 * 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.

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 This position is not available for immediate hire. Shift: Monday- Friday 12:30pm- 6:30pm Pay Range: $21/Hr.- $27/Hr. 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 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.

Tremco Construction Products Group (CPG), part of RPM International Inc., unites industry-leading building envelope solutions manufacturers, service providers, and trusted brands-including Tremco, Nudura, Dryvit, Willseal, Weatherproofing Technologies, Inc., and Weatherproofing Technologies Canada-to deliver comprehensive, integrated building systems. With operations spanning North America, Europe, Asia-Pacific, India, and Latin America, Tremco CPG has a global presence supported by regional businesses and distributors who understand local market needs for commercial, industrial, and residential construction and restoration projects. GENERAL PURPOSE OF THE JOB: Performs visual and physical inspection, sampling, testing, and control of parts, products, and raw materials to conform to established specifications, applicable standards, and the ISO 9001 Quality System. ESSENTIAL DUTIES AND RESPONSIBILITIES: Follows the established quality control procedures to ensure all products are manufactured in compliance with IMS, customer specifications, ISO9001:2015, and ISO14000-2015. Conducts the inspection and testing of raw materials and products, both in process and finished. Performs color quality control and corrections by interpreting results obtained using appropriate measurements. Inspects, calibrates, and supervises the use of various instrumentation for testing. Performs data analysis and provides feedback and improvement suggestions to plant personnel, production management, QC Supervisor, and Quality Assurance Manager on all issues concerning quality. Maintains Quality Control documents and daily reporting of information. Assists in complaint investigations by performing tests to detect or duplicate issues observed in the field. Assists in troubleshooting machine functions and production issues as they arise. Maintains a clean and organized work area. Performs other duties as assigned. EDUCATION REQUIREMENT: High school diploma or general education degree (GED). EXPERIENCE REQUIREMENT: A minimum of 1-2 years of experience in a quality control role within a manufacturing environment with oversight of both raw materials and finished goods. OTHER SKILLS, ABILITIES, AND QUALIFICATIONS: Microsoft Office Suite. Previous experience using enterprise software such as SPA is preferred. PHYSICAL DEMANDS: Incumbent must be able to stand, walk, sit, use hands, reach, climb, balance, kneel, talk, hear, and lift up to 50 lbs. BENEFITS AND COMPENSATION: The hourly rate for applicants in this position generally ranges between $19.57 and $23.00. This range is an estimate, based on potential employee qualifications, operations, needs, and other considerations permitted by law. The Company offers a variety of benefits to its employees, including but not limited to health insurance, paid holidays, paid time off, 401(k) Savings and Trust & Plan with company match, Company Pension Plan, Performance-Based Bonus/Commission, and continuing education. All qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Do you look forward to a new challenge each day in a fast paced ever changing environment?Are you good at organizing information and are interested in working in a manufacturing environment? Do you enjoy using your skills and learning new ones and helping a team reach its goals? If you said yes, then our Quality Control Technician role at The Town Dock might be right for you! The Quality Control Technician is responsible for completing precise raw whole squid and prepared calamari product quality assessments, data entry, daily plant inspections, and equipment sanitation and calibration accuracy checks. Additional responsibilities include, but are not limited to, reporting quality and policy deviations, operating a fryer for calamari taste tests, and providing real-time feedback to the Operations team during in-line quality checks and boat unloading. Specific day-to-day activities depend on boat arrivals and catch volumes (hails). Responsibilities for this position include (but are not limited to): Complete daily pre-Operational (pre-op) sanitation plant inspections, environmental swabbing, and paperwork for the interior and exterior of the plant, communicate corrective actions to the Operations team leadership immediately, and verify the assigned corrective actions were done in the agreed-upon timeframe Complete cooler checks and associated paperwork twice per day and report any deviations immediately Sample and grade raw whole squid during processing and boat unloading against specifications, such as external quality, internal quality, appearance, aroma, texture, count per pound, weight, length, width, and others as needed Upload photographs of raw whole squid samples, enter all quality data to assigned computer location, and report results to assigned individuals the same day as the evaluation Conduct daily calibration accuracy checks for equipment such as thermometers and scales and report any deviations immediately Perform quality control assessments of prepared calamari products against specifications, such as appearance, aroma, texture, taste, count per pound, net weight, glaze percent, size, and defects Upload photographs of prepared calamari samples, enter all quality data to assigned computer location, and report results to assigned individuals the same day as the evaluation Check in-line samples and rework against specifications and report status to Operations immediately Fulfill sales samples requests by picking orders, packing them appropriately for the product and outside temperature, and arranging shipping and pick-up as needed Clean and sanitize work stations to standard regularly Perform other job-related duties as assigned. Requirements Ideal candidate will have: Associates degree in a science curriculum or work equivalent Prior experience in a quality control role, food industry experience preferred. Self-starter with organized and detailed work habits and excellent time management skills Driven to work collaboratively with a preventative mindset. Attention to detail. Ability to perform repetitive tasks Ability to be seafood HACCP certified Available to work a set 5-day schedule in Narragansett with opportunity for rotating on-call overtime as needed Ability to travel to New Bedford for a set rotating on-call summer schedule as needed Proficient math skills Proficient computer skills including MS Office, especially Excel Physical abilities: climb ladders to inspect equipment, lift 30 lbs., and stand for long periods of time in cool temperatures and wet manufacturing environments Flexibility in planning to accommodate the quick changes in seafood production Good communication skills (verbal and written) in English required, Spanish a plus A strong belief and commitment to continuous learning and improvement, positive attitude, teamwork, accountability and ethical behavior. Salary Description $20-$23/hour

The Quality Control Technician will assist the Quality Control Supervisor with the implementation and monitoring of the Quality Management System (QMS). They will also be responsible for inspecting and auditing the manufacturing lines for proper product specification, product quality, and packaging quality. RESPONSIBILITIES AND DUTIES: The Quality Control Technician will: Assure the Edesia is adhering to all relevant international, state and local food manufacturing regulations and help to maintain BRC certification Monitor sanitation, safety regulations and procedures, GMPs and HACCP, FSMA and BRC Standards. Ensure and educate employees on food safety, BRC and quality standards; provide real time feedback to production line workers to make necessary corrections Perform on-line production floor checks at a minimum of every 2 hours throughout duration of shift. Sample and inspect finished product for safety, quality and organoleptic to assure compliance to customer specifications Check label and packaging for correct code dates, product size, clarity, product, and customer Conduct bench analysis for nutrient and physical parameters Prepare necessary laboratory titrations Record inspection and testing data such as weights, temperatures, package integrity checks, water activity, chloride, and vitamin C Perform ATP swabbing of surfaces and equipment Perform the daily Quality Pre-Operational line clearance inspections and documents the inspection Communicate issues and important information to the appropriate person immediately Peer review to confirm that all the documentation is recorded correctly (including sanitation paperwork and operation quality check paperwork) Collect and manage all finished product samples for micro testing, retains, sample library, and other analytical testing or customer requirements Check and record cooler temperature, once per shift Perform CCP verification checks Prepare and perform stability testing and analysis of finished products Identify and isolate finished product that does not meet standards Conduct GMP inspections throughout the facility and communicate findings to supervisor and staff Receive, sample, inspect and test bulk oil deliveries Maintain inventory of lab supplies, and order as needed Solve quality issues on the production floor when they arise Other QA tasks and production-support tasks as assigned