Laboratory technician jobs in Tonawanda, NY - 189 jobs

The University at Buffalo School of Management is seeking an organized and collaborative Operations & Lab Coordinator to support two key initiatives within the School-the Behavioral Research Lab and the Center for Supply Chain Analytics ( CSCA ) . This position splits its time between supporting lab operations for the Behavioral Research Lab and providing operational support for the CSCA . The coordinator will assist with study development and execution, manage lab technology and participant recruitment, coordinate events and communications, supervise student assistants, and oversee day-to-day operations. For the CSCA , the role also supports execution of the Supply Chain Activation Network ( SCAN ) grant, which is a component of the NY SMART I-Corridor Tech Hub. Key Responsibilities: Coordinate daily operations and logistics across the Behavioral Research Lab and CSCA . Support planning and execution of events, workshops, and outreach initiatives. Lead participant recruitment and scheduling for research studies, including SONA system management and outreach. Manage and maintain lab software and technology, including Qualtrics, SPSS , iMotions, and related systems, to ensure functionality and technical support for research. Assist faculty and students with study design, IRB submission, and research documentation. Recruit, train, and supervise student employees and research assistants for both areas. Maintain tracking and reporting systems for projects, research studies, and grant deliverables. Support execution of the SCAN grant and related Tech Hub activities through event coordination, project tracking, and communication. Respond to inquiries from students, faculty, and external partners, providing timely information and logistical support. Perform other operational, research, and administrative duties as assigned. Work Schedule: Monday - Friday, with occasional evening or weekend hours required for events or studies. Learn more: Our benefits , where we prioritize your well-being and success to enhance every aspect of your life. Being a part of the University at Buffalo community. As an Equal Opportunity / Affirmative Action employer, the Research Foundation will not discriminate in its employment practices due to an applicant's race, color, religion, sex, sexual orientation, gender identity, national origin and veteran or disability status. Minimum Qualifications Bachelor's degree in Psychology, Management, Hospitality, Clinical Research, or a related field Preferred Qualifications Graduate degree preferred. Experience with participant recruitment, lab coordination, supervising research assistants, event planning, and project management. Familiarity with Qualtrics, SONA , SPSS , iMotions, and similar software.

As a Research Technician here at Solstice, you will conduct experiments, collect data, and maintain lab equipment, ensuring accurate research findings to drive innovation and new technologies. You will report directly to our R&D Supervisor and you'll work out of our Buffalo, NY location on a On-Site work schedule. **Key Responsibilities:** + Perform laboratory experiments up to kilo-scale involving hazardous materials under the direction of a Chemist or Chemical Engineer + Work includes support for lab experiments, calculations, data analysis, maintaining records, and accurate reporting of data + Perform troubleshooting on kilo-lab scale equipment + Perform routine lab HSE and HOS tasks **BENEFITS OF WORKING FOR SOLSTICE ADANVED MATERIALS** In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Solstice Advanced Materials employees are eligible for a comprehensive benefits package. This package includes employer-subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. **COMPENSATION** This is a Union position where the starting pay is $40.59 per hour. **Responsibilities** **Qualifications** **You Must Have:** + Minimum of a two-year chemistry related degree is required, we value four-year chemistry related degree. + Must be able to work safely with hazardous materials including hydrofluoric acid (HF), fluorosulfonic acid (FSA), etc. + Must have good chemical knowledge and mechanical aptitude to assemble, run and troubleshoot chemical experiments and equipment + Must demonstrate ability to learn and use analytical equipment needed in support of processes including Gas-chromatograph and other laboratory instruments + Be able to use computer software such as Microsoft Office applications (Outlook, Word, Excel), and process control software + Be able to move up to 600-pound drums and 250-pound gas cylinders utilizing appropriate handling equipment, lift and carry up to 35-pound pails, climb ladders and scaffolding, wear all PPE and respiratory equipment + Be able to work rotating 8-hour shifts + Must demonstrate ability to learn and use analytical equipment needed in support of processes including Gas-chromatograph and other laboratory instruments **ABOUT SOLSTICE** Solstice Advanced Materials business unit focuses on developing innovative materials that are environmentally friendly and enhance product performance. This unit is dedicated to creating solutions that meet the evolving needs of various industries while promoting sustainability and efficiency. Our commitment to research and development drives the creation of advanced materials that support a wide range of applications, ensuring we remain at the forefront of technological advancements. _Solstice is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status._ **About Us** **About Solstice Advanced Materials** Solstice Advanced Materials is a leading global specialty materials company that advances science for smarter outcomes. Solstice offers high-performance solutions that enable critical industries and applications, including refrigerants, semiconductor manufacturing, data center cooling, nuclear power, protective fibers, healthcare packaging and more. Solstice is recognized for developing next-generation materials through some of the industry's most renowned brands such as Solstice , Genetron , Aclar , Spectra , Fluka, and Hydranal. Partnering with over 3,000 customers across more than 120 countries and territories and supported by a robust portfolio of over 5,700 patents, Solstice's approximately 4,000 employees worldwide drive innovation in materials science. For more information, visit Advanced Materials (********************************************** . **Job Identification** 105930 **Job Category** Integrated Supply Chain **Job Schedule** Full time **Locations** 20 Peabody St, Buffalo, NY, 14210, US **Hire Eligibility** Internal and External **Relocation Package** None

This is a full time, non-exempt level position. Collecting and distribution of samples Physical testing of production samples Daily calibration of standard lab instruments Recording and interpreting test results Verifying sufficient inventory of testing supplies Maintaining the cleanliness of the laboratory environment Maintains samples of tested product in order to confirm test results when necessary Performs light maintenance and calibration on all ADM laboratory equipment. Maintains ongoing records of the results of all testing procedures and inputs such data into computer daily Maintains adequate supplies used for testing and notifies the supervisor of the need to re-order such supplies Continually compares test results with standards as required to insure that all flour is within specification Notifies appropriate colleagues when product is not within specification Job Requirements: Understands most production processes required in the production of flour and how it would relate to analysis being performed Maintains a neat and clean working area at all times, washing equipment as required and placing equipment in the proper storage areas Maintains an effective working relationship with fellow employees Performs duties in a safe manner, utilizing all approved safety equipment and successfully completes all safety certification requirements Maintains awareness and adheres to all FDA, GMP, BATF, EPA, OSHA and employer standards and guidelines Handles various chemicals in assorted containers in the manner outlined in the manufacturer's chemical Material Safety Data Sheet Informs supervisor immediately of any hazards, unsafe equipment and/or acts Additionally reports immediately any accidents, injuries and near misses to supervisor Recommends solutions to correct deficiencies or improve work and operational practices Participates actively in training Reports to work in a condition to be able to perform all duties Practices proper personal hygiene Familiarizes themselves with the hazards in their work area and how to protect themselves Understands that accidents are preventable and that safety is everyone's responsibility Dedication to ADM's goal of achieving a zero injury culture; understand and follow company safety procedures Exhibit regular and prompt attendance Cross training with other Laboratory manager Work shift work including nights, weekends, and holidays Physical Requirements: Prolonged periods of standing and sitting Working in confined spaces and from heights, bending, kneeling, climbing stairs and ladders Working in a variety of conditions (heat, cold, dust, etc.), lift up to 50 lbs. unassisted Before applying for an exempt, non-exempt or hourly job opportunity, you are expected to initiate a discussion and share your intentions with your supervisor. * If you've been in your current position for more than 18 months, supervisor approval is not required. * If you've been in your current position for less than 18 months, verbal supervisor approval is required. Hiring Manager- Francis Campbell Recruiter- Lauren Shea About ADM At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We're a global leader in human and animal nutrition and the world's premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at ************ Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. If hired, employees will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. The pay range for this position is expected to be between:

HOURLY RANGE: $43.31 - $54.64 DISTINGUISHING FEATURES OF THE CLASS: The work involves supervising and performing multiple tests or examinations on patient specimens in a clinical laboratory using defined procedures to aid in the diagnosis or treatment of patients at Erie County Medical Center Corporation (ECMCC). This class differs from that of Clinical Laboratory Technologist by virtue of its supervisory responsibilities and performance of more difficult and complex laboratory tests. Work is performed under the general supervision of the Chief Clinical Laboratory Technologist for the assigned clinical section. Supervision is exercised over lower-level technical employees. Does related work as required. TYPICAL WORK ACTIVITIES: Supervises and performs a number of routine and special tests according to established procedures in two or more clinical laboratory sections: Biochemistry, Blood Bank, Hematology and/or Microbiology/Diagnostic Immunology; Performs more difficult and complex tests and examinations according to established procedures in two or more clinical laboratory sections; Evaluates and interprets laboratory test data as to necessity for further process of specimens utilizing laboratory information system (LIS); Performs quality control as needed to ensure accuracy of instrument function and appropriateness of reagents used in patient testing; Investigates quality control problems that cannot be fixed by lower-level staff; determines and performs such fixes; Assists with research and developmental/special studies; Maintains equipment and supplies of section(s); Maintains records of sections(s) and prepares reports; Performs other activities that contribute to patient care and/or maintenance of compliance with various regulations; Supervises lower-level staff by making assignments, reviewing and evaluating work performance; Supervises making of solutions and reagents, setting up of equipment and maintenance of equipment and supplies; Assists in the education and training of technical personnel and students through demonstrating procedures, overseeing work practice and evaluating progress; Keeps abreast of latest developments in the field; Collects specimens from patients, which may include phlebotomy. FULL PERFORMANCE KNOWLEDGES, SKILLS, ABILITIES AND PERSONAL CHARACTERISTICS: Thorough knowledge of principles, practices, techniques, terminology and equipment as applied to a clinical laboratory; good knowledge of quality control and quality assurance procedures as applied to a clinical laboratory including verification and validation procedures; good knowledge of applicable laws, rules, regulations, accreditation standards and ECMCC policies and procedures as they relate to a clinical laboratory; good knowledge of laboratory and hospital information systems; ability to perform difficult and complex clinical laboratory work with a high degree of accuracy; ability to exercise safety precautions in handling infections and biologically active specimens and in using clinical laboratory equipment; ability to supervise and train others; ability to maintain accurate records of test results and prepare clinical laboratory reports; ability to make minor repairs and maintain clinical laboratory equipment; ability to understand and follow both oral and written instructions; ability to analyze and interpret clinical laboratory findings, both orally and in writing; ability to establish and maintain effective working relationships with a diverse constituency; ability to utilize a variety of electronic software applications; sound professional judgment; capable of performing the essential functions of the position with or without reasonable accommodation. MINIMUM QUALIFICATIONS: * ) Possession of a Master's Degree* in Clinical Laboratory Technology, Medical Technology or related title that meets the standards set forth in Title 8, Article 165 of New York State's Education Law and Subpart 79-13 of the Regulations of the Commissioner of Education and two (2) years' experience in the clinical laboratory section for which appointment is sought; or: * Possession of a Bachelor's Degree* in Clinical Laboratory Technology, Medical Technology or related title that meets the standards set forth in Title 8, Article 165 of New York State's Education Law and Subpart 79-13 of the Regulations of the Commissioner of Education and four (4) years of technical clinical laboratory experience (in accordance with New York Code, Rules and Regulations, Title 10, Part 58-1.4)*, of which two (2) years were in the clinical laboratory section for which appointment is sought; or: * Possession of a license to practice as a Clinical Laboratory Technologist as issued by the New York State Education Department and four (4) years of technical clinical laboratory experience (in accordance with New York Code, Rules and Regulations, Title 10, Part 58-1.4), of which two (2) years were in the clinical laboratory section for which appointment is sought. SPECIAL REQUIREMENTS: Possession of a license to practice as a Clinical Laboratory Technologist as issued by the New York State Education Department at time of appointment and maintenance throughout duration of appointment. NOTE*: Your degree must have been awarded by a college or university accredited by a regional, national, or specialized agency recognized as an accrediting agency by the U.S. Department of Education/U.S. Secretary of Education. If your degree was awarded by an educational institution outside the United States and its territories, you must provide independent verification of equivalency. A list of acceptable companies who provide this service can be found on the Internet at ******************************************* You must pay the required evaluation fee. NOTE 2: Verifiable part-time and/or volunteer experience will be pro-rated toward meeting full-time experience requirements. @Approved by Erie County

Medical Technologist/MLS or Medical Laboratory Technician Opening at one of New York's Top Healthcare Providers! This organization is looking to add a permanent and full time Medical Technologist/ Medical Laboratory Technician to their team on either day, evening or night shift! They also have department specific openings in blood bank, microbiology, core laboratory or special chemistry! This facility is offering a highly competitive hourly rate and a top notch benefits package! Benefits include: Medical Dental and Vision, Retirement Benefits, Generous PTO, Recognition and Reward Programs and ample opportunity for Career Development! Sign on bonus and/or Relocation Assistance is also available! Interested in learning more? Contact Marina at marina@ka-recruiting.com or call/text 617-430-7080!

Ready for more than just a job? Build a career with purpose. At Lactalis in the USA, we're committed to providing meaningful opportunities for our people to learn, grow, and thrive-whether you're just starting your journey with us or looking to take the next step in your career. From day one, we offer the tools and support to help you succeed. As the world leader in dairy, Lactalis is a family-owned company with over 85,000 pragmatic and ambitious professionals across the globe. Each day, we're proud to produce award-winning dairy products that bring people together. In the US, we proudly offer an unrivaled house of beloved brands, including Galbani Italian cheeses and ricotta, Président specialty cheeses and butters, Kraft natural and grated cheeses, Breakstone's cottage cheese, Cracker Barrel , Black Diamond cheddar, and Parmalat milk. Our yogurt portfolio includes siggi's , Stonyfield Organic , Brown Cow™, Oui , Yoplait , Go-Gurt , :ratio , Green Mountain Creamery , and Mountain High , along with a growing family of ethnic favorites like Karoun , Gopi , and Arz . At Lactalis, we live by our core values-Ambition, Engagement, and Simplicity. We foster a workplace where innovation thrives, diverse perspectives are celebrated, and everyone's unique background and ideas are valued. Even if you don't meet every qualification, we encourage you to apply. We want to hear about your PASSION, your STORY, and how your EXPERTISE can help us shape the future of dairy. From your PASSION to ours Lactalis American Group, part of the Lactalis family of companies, is currently hiring a Lab Technician based in Buffalo, NY. Lab Technician 1 will be responsible for a variety of activities that support and provide technical assistance to Research and Development, Corporate Plants, and Corporate Quality Assurance. Perform routine testing on all Liquid and Solid samples provided to the lab from Plants, QA, and R&D, including company samples and competitor samples as provided by Marketing and Sales. From your EXPERTISE to ours Key responsibilities for this position include: Perform all analytical tests to properly evaluate each product provided to the laboratory. Testing to include, but is not limited to Fat, Moisture, Calcium, Salt, Protein. Sample and provide assistance to have samples tested, when required, at an outside lab for chemistry and microbiology. Provide all analytical data results to Lab Manager and or/Project Manager in an organized and clear format. Carry out daily, weekly and monthly cleaning of analytical equipment and laboratory area. Monitor chemical reagents and notify Lab Manager when supplies are running low. Work closely with laboratory staff. Provide technical assistance as needed for Aware of and practice Plant's Good Manufacturing Practices (GMP) as well as Good Sanitation Practices (GSP). Working Conditions Extended hours may be necessary depending on the project needs.To fulfill these responsibilities, tools such as a computer, phone or, and / or allowance(s) may be provided. Reasonable accommodations may be made to enable individuals with disabilities to perform these essential duties and responsibilities. This position requires physical presence in the plant/office. Demonstrate commitment to a safe working environment that promotes the health and well-being of all employees and that will further contribute to the Company's overall performance and success. Requirements From your STORY to ours Qualified applicants will contribute the following: Education Associates degree in Dairy Science preferred. Equivalent experience acceptable. Experience 2+ years dairy science experience is favored. Must minimally have laboratory experience. Certifications and specific knowledge Solid working knowledge of basic laboratory skills Good mathematical skills are required (calculate averages) Food industry knowledge is preferred. Working knowledge of Word, Excel, and Power point for report At Lactalis, we offer a comprehensive Total Rewards Program with a variety of affordable benefits and coverage options. We support insurance costs significantly, contribute generously to retirement plans, and offer Paid Time Off from day one. We are committed to your professional growth, providing training and development opportunities, including Education Reimbursement. Join us and grow your career. Lactalis is an equal employment opportunity employer. We will not discriminate against applicants with regard to any legally-recognized basis including, but not limited to: veteran status, race, color, religion, sex, national origin, age, marital status, sexual orientation, and physical or mental disabilities. Further, any division of the Company that is an Affirmative Action Employer will comply with all related legal obligations. Salary Description $25 - 27 Hourly

Are you a self-driven person looking to advance your career as a high-impact player on a team? If so, we have an exciting challenge for you and your future! Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness. We offer a competitive benefits package that includes health, dental, vision, wellness programs, employee discounts, retirement plans, tuition reimbursement, ongoing development, advancement opportunities and more. Founded in 1846, today HP Hood is one of the largest and most trusted food and beverage manufacturers in the United States. Our portfolio of national and super-regional brands and licensed products includes Hood, Heluva Good, Lactaid, Blue Diamond Almond Breeze, Planet Oat and more. Job Summary: The Lab Technician will handle all aspects of the lab including chemical testing, bacteria testing and quality assurance to ensure the manufacture and packaging of high quality products. Shift: Alternating 3 or 4 day work weeks. 12 hour shift beginning at 5:00pm EST. Essential Duties and Responsibilities: Laboratory testing to meet standards set up in PMO, Standard Methods for the Dairy Industry and FDA 2400 methods requirements. Pulling, logging, and running finish product and processing samples for all test required on each product. Pull sample of incoming raw material and packaging to determine acceptability of loads from our suppliers. Audit CIP chemical concentrations and ensures compliance to company specifications. Must be able to prepare media and other lab controls. These would include but are not limited to pour plates, buffer water, etc. Operate autoclave to sterilize plates and equipment as needed while ensuring sterility test are accurate. Assist in lab equipment PMs such as cleaning the Micro Luminescence Systems weekly with caustic; drain and clean the autoclave bi-weekly; changing fluid standards and filters on the cryoscopy. Inoculating batch tanks with enzyme and vitamins and recording usages on the various logs. Responsible for the daily cleanup and review of racking systems in the incubators and cooler to set up for shelf life testing. Participate in environmental testing in and around plant that includes swabbing, air plating, water sampling, etc. Verifies that plant equipment meets sanitation requirements prior to start up. Various tasks involving the responsibility of the food safety and quality of company products. Education and Experience: Prior experience in food manufacturing. Knowledge of food microbiology, chemistry, dairy standards and CIP sanitation. Intermediate Computer Skill (i.e. Word, Excel, etc.) Ability to work well with people. Communication skills are a must. Multi-tasked Individual. Ability to work independently. Physical Requirements: Ability to move throughout all areas of the facility including but not limited to office, production, and warehouse environments. Including the outside perimeter of the building. Able to work at heights greater than 40 feet while operating a powered industrial truck. Able to wear all necessary personal protective equipment to perform job functions. Stand and/or sit continuously and perform job functions for a full shift with meal break. Physically able to stand, bend, stoop, kneel, reach, twist, lift, push, pull, climb, balance, crouch, handle and move items weighing up to 50 pounds without assistance and move objects exceeding 50 pounds with reasonable accommodations. Visual acuity corrected to perform job functions. Exact compensation may vary based on skills, experience and location. The pay range for this position is $27.98 - $28.64 USD HP Hood is an Equal Opportunity Employer Female/Minority/Veteran/Disabled "VERVRAA Federal Contractor" CCPA For Applicants in Massachusetts - It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Employment is subject to verification of an applicant's identity and eligibility for employment in the United States as required by immigration laws. We are unable to assist with sponsorship at this time.

HWI has a fantastic opportunity to join our Quality Team as a Facility Quality Assurance Technician. The Facility Quality Assurance Technician supports HWI's mission and vision to drive industry performance and deliver quality results. This role focus is on the actual testing of product and raw materials, judging samples against standards and accurately enters data into our Laboratory Information Management System (LIMS). A successful candidate will maintain high level of accuracy and engagement to guide HWI towards achieving and exceeding their objectives. Responsibilities Verify in process production. Performs physical testing of finished goods. Performs final inspections. Enters LIMS data into appropriate systems and judges acceptability of product. Screens analysis of raw materials and mixes. Sample preparation. Performs additional testing as required. Requirements Requires high school diploma and one (1) year of college education or technical training with emphasis on math and science. Requires computer operation aptitude (MS Office and LIMS system or similar products). Requires abilities to follow directions, provide innovative solutions, and both work independently or as a team member. Requires knowledge of refractory industry and quality assurance. Physical and Environment Requirements: Physical Activity: Requires less than 1/3 of time sitting, climbing/balancing, and stooping/kneeling/crouching/crawling. Requires 1/3 to 2/3 of time walking, using hands and fingers, reaching, and speaking/hearing. Requires more than 2/3 of time standing. Lifting: Requires lifting up to 25 pounds 1/3 to 2/3 of time, and lifting up to 50 pounds more than 2/3 of time. Vision: Requires accurate close vision, color vision, and the ability to focus. Environment: Requires 1/3 to 2/3 of time in an office setting and working near moving mechanical parts. Also requires less than 1/3 of time in wet/humid conditions, working in high, precarious places, exposed to fumes or airborne particles, vibration, outdoor weather, and in extreme heat or cold. Noise: Requires exposure to moderate noise.

* This position involves performing X-Ray Fluorescence (XRF) analysis and other analytical methods to determine major, minor, and trace elements in raw materials, plant products, and materials submitted by customers and clients using established methods and procedures. Responsibilities * Perform spectroscopic analysis and other analytical methods using computer-controlled X-Ray spectrometer, including all ancillary equipment and software. * Accurately weigh samples and prepare them for analysis using methods such as fused bead, pressed pellet, and loose powder, while properly maintaining platinum sample preparation materials. * Utilize appropriate calibration, correction standards, and quality control criteria to ensure data precision, repeatability, and accuracy. * Archive and dispose of samples, recognize instrumental and equipment issues, assist with routine maintenance service and repairs, and maintain and order supplies when necessary. * Continuously evaluate, modify, and improve existing methods and create new methods for sample evaluation and analysis. * Communicate with plant production group and technical staff to obtain analytical schedules and priorities. * Maintain accurate records of analysis and report findings and test results, entering data into the Quality Control Database. * Provide occasional weekend coverage based on production needs. * Perform other duties as assigned. Essential Skills * Minimum two-year college degree in chemistry, chemical technology, or equivalent experience in chemistry. * Understanding of X-ray spectroscopy theory and familiarity with WD-XRF unit and ZSX quantitative and SQX semi-quantitative software. * Full understanding of quality assurance and quality control practices. * Knowledge of ISO 9001:2015 and its application in the workplace and lab activities. Additional Skills & Qualifications * Strong mathematics and computer skills with familiarity of Microsoft Office 365 software. * Effective time management skills to manage priorities, turnaround time, and production requirements. * Ability to work independently and in a team environment. * Interpersonal skills to interact with staff, clients, and vendors. * Written and oral communication skills for recording and reporting analytical data, preparing documentation such as SOPs, and training QC technicians. * Ability to diagnose and perform minor repairs and upkeep of instrumentation. * Capability to recommend equipment purchases and maintain stock of specialized consumables. Work Environment * This role is based in an industrial lab setting with less cleanliness. * The work schedule is Monday through Friday from 7am to 3:30pm, with occasional weekend work required based on production needs. * Benefits include company-paid life insurance, an annual safety shoe allowance, and uniform availability. Job Type & Location This is a Contract to Hire position based out of Niagara Falls, NY. Pay and Benefits The pay range for this position is $20.00 - $25.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Niagara Falls,NY. Application Deadline This position is anticipated to close on Jan 19, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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: $152,290.00 - $250,195.00 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 *************. Please note: this resource is for accommodation requests only. For all other inquires related to your application and careers at Guardian, refer to the Guardian Careers site. Visa Sponsorship Guardian is not currently or in the foreseeable future sponsoring employment visas. In order to be a successful applicant. you must be legally authorized to work in the United States, without the need for employer sponsorship. Current Guardian Colleagues: Please apply through the internal Jobs Hub in Workday.

Buffalo News Names Sealing Devices Inc. A Winner of The Metro Buffalo Top Workplaces 2024 Award Statement of Work: * Follow all company policies, procedures, and work instructions in the completion of daily activities with minimal input and supervision to ensure successful accomplishment of company objectives. * Perform Receiving Inspections to verify that incoming parts, materials, and related documentation meet requirements and are suitable for use. * Perform First piece, In-process, Last piece, and Final inspections per sampling plans, product requirements, and job instructions to verify product conformity. * Perform First Article Inspections to ensure manufacturing die, tooling, and other manufacturing methods result in product meets customers drawing requirements. * Perform customer specific required Inspections and complete Inspection reports per the stated requirements. * Document, identify, and segregate nonconforming product in accordance with policies, procedures, and work instructions. * Complete and submit customer documentation as required. * Document, identify and segregate nonconforming product in accordance with policies, procedures and work instructions. * Make requests to suppliers for missing or incorrect documentation. * Use appropriate measuring devices and automated inspection equipment to perform inspections including basic programming of automated inspection equipment. * Interact with other departments in a professional manner in addressing product quality and service issues. * Provide other departments with information and assistance to support them in accomplishing their objectives. * Contribute to and participate in improvement activities within the department and the company. * Follow departmental procedures and work instructions as written and recommend improvements as necessary. * Perform any other task/activity assigned by the supervisor within the scope of Company business. * Maintain a safe and clean working environment by complying with policies, guidelines, and regulatory requirements per the Sealing Devices Quality System What you will need to Succeed: * High School Graduate or General Education Degree (GED): Required * Associate's Degree (two year college or technical school) or Work Equivalent, Field of Study: Industrial Technology or Quality related field * Bachelor's Degree (four year college or technical school) Preferred, Field of Study: Industrial Technology or Quality related field * Computer Literacy (MS Office), 2 plus years of experience in mechanical inspection and blueprint reading required. * Knowledge of GD&T, basic statistical techniques, automated inspection experience preferred. * ASQ Certified Quality Technician (CQT) preferred Benefits offered for this role: * Medical/Dental/Vision Coverage * Health Reimbursement Account (HRA) provided by Company * 401K * Paid Vacation & Holidays * Free Life Insurance for Employee * Flex Spending - Medical, Dental, Vision and Child Care * Employee Referral Program * Company Sponsored Training * Profit Sharing - Earn up to 18% of your gross wages after one-year anniversary * Free Employee Assistance Program * Wellness Programs - Onsite Reflexology, Chair Massage, Nutritional Sessions, Chiropractic * Legal Shield and Aflac * Employee Recognition Program * Company Celebrations - Including: Lunches, Breakfasts, Ice Cream Truck, Holiday Parties * Career Advancement Opportunities 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. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. * Ability to sit or stand for extended periods of time while performing detailed inspections and working at inspection stations. * Regularly required to lift, carry, and move materials or product up to 25 pounds; occasional lifting of heavier items with assistance. * Frequent use of hands and fingers to handle small parts, operate measuring instruments, and input data into computer systems. * Ability to perform repetitive motions of the wrists, hands, and arms during part handling and equipment use. * Requires close vision, color vision, peripheral vision, depth perception, and the ability to adjust focus for precision inspection tasks. * Must be able to hear verbal instructions, alarms, and signals in a manufacturing environment. * Occasional reaching, stooping, bending, turning, or crouching to retrieve or position parts and materials. * Ability to work in both office and production environments, which may involve moderate noise levels, temperature variation, and use of personal protective equipment (PPE) when required. Salary ranges for this position are determined based upon the job location and can be adjusted based upon experience, reflecting our commitment to valuing the expertise and contributions of our individual team members. Salary range for this role is $22-27/hr based upon experience.

Job Description Our Company Biocare Medical, LLC is an innovator in developing and supplying world class automated immunohistochemistry instrumentation, and the full range of reagents for IHC lab testing. Biocare specializes in high quality IHC, ISH, and FISH slide staining through its brand-new automated instrument, NeoPATH Pro™, and offers best-in-class simultaneous Multiplex IHC solutions. The company's customers include clinical histology laboratories, pharmaceutical companies, CROs, biotechnology companies as well as academic, government, military, and non-profit laboratories. Biocare Medical offers an expanding portfolio of integrated products to address the rapidly growing cancer and infectious disease diagnostic and research markets with novel tissue immunohistochemistry and in situ hybridization methods. Biocare Medical is headquartered and has manufacturing facilities in California with a global distribution network. Summary/Objective The Laboratory Technician supports all stages of the probe manufacturing process-from sample preparation to final quality assessment-to ensure the production of high-quality molecular diagnostic products. This role involves performing hands-on laboratory work, maintaining reagents and bacterial clones, and operating both manual and automated instrumentation. The ideal candidate thrives in a fast-paced environment, values accuracy and consistency, and takes pride in producing results that meet exacting quality standards. Daily responsibilities include reagent preparation, DNA isolation, equipment upkeep, and documentation of results, all in accordance with laboratory SOPs and safety policies. Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Perform DNA isolation and probe production using both manual and automated techniques. Maintain precise documentation of production processes, probe performance, and quality control results. Execute established quality control procedures, calibrations, and preventative maintenance on laboratory instruments. Follow the laboratory's standard operating procedures (SOPs), policies, and regulatory requirements. Identify and troubleshoot issues that could impact production quality or turnaround times. Implement and document corrective actions when systems deviate from performance specifications. Conduct quality testing of reagents and ensure proper labeling, storage, and inventory management. Support process improvements to enhance efficiency, reliability, and consistency of results. Maintain a safe and compliant work environment through strict adherence to company safety policies. Perform additional laboratory assignments and cross-functional projects as directed by management. Competencies Bachelor's Degree required. Minimum one (1+) year experience in a commercial lab environment preferred. Technical Expertise: Proficient in molecular biology, DNA isolation, and probe-based methodologies. Quality Focus: Committed to maintaining high laboratory standards and regulatory compliance. Attention to Detail: Demonstrates precision in recordkeeping, testing, and data accuracy. Analytical Thinking: Uses sound judgment to assess issues and determine effective resolutions. Collaboration: Works cooperatively within team environments to achieve production goals. Adaptability: Adjusts effectively to shifting priorities, workloads, and new technologies. Compensation Range $20 - $23 hourly Position Type & Expected Hours of Work Full-time Onsite Position 8:00 a.m. to 5:00 p.m. Monday - Friday. This position may require extended weekday or weekend hours depending on business needs. Full-Time Positions Offer Company Sponsored Health Insurance - Medical, Dental, Vision Company Sponsored Life Insurance Voluntary Benefits Retirement plan with a match - 401(k) PTO Paid Holidays EAP BioCare Medical values the diversity of individuals, ideas, and perspectives, and what they bring to the workplace. We know that our people represent the future of the company, so we only hire the best from around the world. Applications from all qualified candidates will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, physical or mental disability, or status as a Protected Veteran. All inquiries strictly confidential.

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse, Will work with hazardous/toxic materials Job Description As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: First Shift: Monday - Friday 7am - 330pm (may require start and end time flexibility based on training and production needs) The Thermo Fisher Scientific BioProduction division, located at 3175 Staley Road Grand Island NY 14072, supports developers and manufacturers of biological-based therapeutics and vaccines with a portfolio of premium cell culture media and buffers as well as on site custom services dedicated to upstream cell culture, downstream purification, analytics for detection and quantitation of process/product impurities, and a catalog of single-use solutions spanning the biologics workflow. How Will You Make an Impact?: We need a motivated individual with excellent communication and laboratory skills to coordinate and complete planned and detailed activities within a quality system to ensure product, process, system, or equipment quality requirements are met. A Day in the Life: Perform wet chemical analyses based on both internal and Compendia (USP, EP, ACS, etc) based methodologies on raw materials (i.e. salts, sugars, amino acids, vitamins, etc) . Perform physical inspection and documentation review of incoming manufacturing components. Education: Required: High School Diploma required Preferred: AAS or Bachelors degree in Chemistry, Biology, or other Sciences Experience: Preferred: Experience in a cGMP environment/QC or QA related field Knowledge, Skills, Abilities: Required: Strong organizational skills and the ability to work independently. Required: Ability to work in a high paced team environment, prioritize work accordingly. Required: General digital literacy, specifically in Microsoft office programs. Preferred: 1-2 years of Chemistry lab experience (wet Chemistry lab work and safety protocols). Physical Requirements / Work Environment: Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Occasionally required to enter Cold Room/Freezers -22degreesF/-6degrees C Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Will work with hazardous/toxic materials What We Offer: Compensation Competitive Pay Performance Related Bonus where eligible Annual merit performance-based increase Excellent Benefits Medical benefits Paid Time Off/Annual Leave Employee Referral Bonus Career Advancement Opportunities Compensation and Benefits The hourly pay range estimated for this position based in New York is $16.95-$25.42. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

The ASVAB isn't the only test that matters in the military. A Soldier's tissue, blood, and body fluids also need to be tested to detect and identify diseases. As a Medical Laboratory Specialist in the Army National Guard, you will perform these clinical tests that the healthcare team will use to diagnose, treat, and prevent illness of their patients. In this role, you will examine blood and bone marrow samples; test for bacteria or viruses; and analyze tissue, blood, and fluid specimens for diagnostic information. Job Duties * Perform elementary blood banking and clinical laboratory procedures in hematology, immunohematology, clinical chemistry, serology, bacteriology, parasitology, and urinalysis * Collect blood specimens by venipuncture and capillary puncture * Pack, unpack, inspect, store, and distribute blood products * Assemble, disassemble, and maintain laboratory equipment Some of the Skills You'll Learn * Medical laboratory procedures * Study of human parasites and diseases * Laboratory administration and record keeping Helpful Skills * Interest in biology, chemistry, and algebra * Ability to follow detailed procedures precisely Through your training, you will develop the skills and experience to enjoy a civilian career with privately owned laboratories, hospitals, clinics, or research institutions. The certifications available to you after continued study and experience are medical laboratory technician, cytotechnologist, and clinical laboratory technician. Specific educational criteria must be met before you can qualify for certification. Earn While You Learn Instead of paying to learn these skills, get paid to train. In the Army National Guard, you will learn these valuable job skills while earning a regular paycheck and qualifying for tuition assistance. Job training for Medical Laboratory Specialist consists of 10 weeks of Basic Training, where you'll learn basic Soldiering skills, and 52 weeks of Advanced Individual Training. Training consists of both classroom and field work.

Job DescriptionQuality Control Technician (2nd Shift - 3:30 - Midnight) Also known as: Quality Inspector, QC Inspector, QA Technician, Quality Assurance Technician, Manufacturing Quality Technician, Welding Inspector, Metal Fabrication Inspector, Structural Steel Inspector, Production Quality Technician Location: Buffalo, NY | Schedule: Monday-Friday, 3:30 PM-12:00 AM | Pay range: 20-25 an hour with Shift differential GTI Fabrication manufactures custom modular structures, energy storage enclosures, and container-based systems for military, defense, energy, and commercial industries. We specialize in metal fabrication, welding, assembly, structural steel, and modular construction at our Buffalo, NY facility. We are hiring a 2nd Shift Quality Control Technician (Quality Inspector / QC Inspector) to perform inspections on welded, fabricated, and assembled components throughout the manufacturing process. Responsibilities Perform incoming, in-process, and final inspections on fabricated metal parts, welds, and assemblies Conduct visual weld inspections and dimensional inspections Read and interpret blueprints, weld symbols, fabrication drawings, and mechanical prints Maintain accurate QC reports, inspection logs, and test data Calibrate and maintain measurement tools and QC equipment Identify nonconformities (NCRs) and communicate issues to supervisors Support continuous improvement for quality assurance and welding quality Work closely with fabrication, welding, assembly, and engineering teams Qualifications 2-5 years of experience as a Quality Control Technician, Quality Inspector, QC Inspector, Welding Inspector, or Manufacturing Quality Technician Experience with weld inspection and metal fabrication inspection Proficiency using calipers, gauges, tape measures, squares, and weld inspection tools Ability to read and interpret mechanical drawings, fabrication prints, and electrical diagrams Strong math skills (fractions, decimals, tolerances) Ability to lift 50 lbs and work in a shop-floor production environment High school diploma or GED Preferred: AWS CWI certification or working toward certification Experience in welding, structural steel, modular manufacturing, or industrial fabrication GrowTech Industries, LLC is an equal opportunity employer. 2nd Shift - Monday-Friday 3:30 - Midnight

Job Description McGard LLC Electroplating Lab Technician Hourly pay rate: $20.00-$25.00/hr plus 20% shift differential About McGard McGard has been a trusted name in the automotive industry for over 50 years. We specialize in manufacturing high-quality, precision-engineered automotive security products and components. Our commitment to excellence, innovation, and customer satisfaction has earned us a reputation as a global leader in our field. Your Schedule 3rd shift, 10:00PM - 6:30AM, Sunday - Thursday Ability to work overtime during the week and Saturdays as needed. Benefits: Competitive wage and comprehensive benefits package: health/dental/life insurances, PTO, quarterly profit sharing, 10 holidays, 401k plan with employer match. Tuition reimbursement program. On-site walking trail and convenience cafeteria. About the Position Assists in set up and maintaining of all parameters of the plating operations. Maintains a deposition of plating of the highest quality for superior marketability and fewer defects. Assist Plating Operators and Utility Workers in ongoing training. Run daily analysis on varied plating processes to ensure proper concentrations and additions. Perform tests, as well as daily data entries to files on baths and various plating properties. Perform various plating baths analysis such as surface tension, brightener, pore count, concentration, stress & tensile testing, pH adjusts, etc. Trouble shoot various plating process issues using laboratory techniques. Operate and calibrate equipment such as electric metering pumps, pH meter indicator, X-ray, etc. Perform plated adhesion tests per customer required specification. Complete internal sample submission testing and reports. Test and report on the quality of internal and outside plating process. Sign off parts release to McGard. Must complete D.O.T. hazardous material training and hazardous material emergency response training (HAZWOP). Run test racks on the R & D plating line. Requirements: High School graduate or equivalent. Strong math and mechanical aptitude. Understand and execute routine written and verbal instructions with minimal supervision. Able to communicate effectively in English both written and verbally. Proven record of exemplary attendance. Strong problem solving and troubleshooting skills. Regular use of a respirator. Must pass Respirator Protection and Fit Testing. Preferred Knowledge/Skills/Abilities: Background of Chemistry education and/or experience. Experience in a lab setting (i.e. knowledge of equipment and procedure). Experience in electroplating process. Growth Be part of an innovative team. Ability to operate in culture of safety. Expand technical capabilities. Working with and learning from experienced operators. Develop leadership skills, that will allow you to focus on acquired knowledge and ability to adopt and implement new ideas. “We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.” #LI-ONSITE IND123

Quality Control Technician - 3rd Shift The Quality Control Technician is a key member of CP Flexible Packaging's manufacturing, quality management team. The role is responsible for ensuring that manufacturing processes and products meet our stringent quality specifications. This role assists the Quality Manager by helping to lead and support a staff of Quality Control Technicians, working on all shifts. The Plant runs on a 24\/7 basis. The ultimate goal of this role is to help the Plant to minimize waste, improve productivity on the production line and ensure that customers receive products that are fit for use. Role To prepare inspection plans and instructions, select sampling plan applications, analyze and solve problems, prepare procedures, train inspectors and perform audits. Processes Quality control technicians help develop processes and procedures for quality control. They decide the standards to be achieved, which may involve complying with recognized systems such as the ISO 9000 \-\- Quality Management system published by the International Organization for Standardization. The QCT trains inspectors to carry out checks in line with procedures and audit their work to ensure they comply with the standards. If they identify problems, they recommend improvements. Data Collecting the right data is essential to quality control. This role helps to define statistical techniques, determine what data needs to be collected through inspection or process monitoring, and analyze results. Interprets the data to identify problems or trends as a basis for planning remedial action. Inspection The Quality Control Technician may at times, personally carry out some of the inspections and\/or oversee the work of quality control inspectors. This role insures that incoming raw materials, components or supplies meet agreed standards by carrying out routine inspections and rejecting unsuitable items. It also performs a wide range of controlled tests on products at various stages of the manufacturing process. Tests include visual inspection or non\-destructive testing to determine conformance with the product's specification. Prevention The Quality Control Technicians plan corrective and preventive actions to maintain quality standards and carry out different types of analyses, including root cause analysis and failure mode and effects analysis (FMEA) to identify the source of problems. QCTs prepare reports and recommendations to deal with any issues that arise. Requirements 2 plus years experience in Quality Control, preferably in plastics\/manufacturing. Benefits Medical Benefits, 401k, PTO, Paid Holidays "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"693189719","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Manufacturing"},{"field Label":"Work Experience","uitype":2,"value":"1\-3 years"},{"field Label":"City","uitype":1,"value":"BUFFALO"},{"field Label":"State\/Province","uitype":1,"value":"New York"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"14210"}],"header Name":"Quality Control Technician \- 3rd shift","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********03517110","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":false,"job Id":"**********00265148","FontSize":"12","google IndexUrl":"https:\/\/cpflexpack.zohorecruit.com\/recruit\/ViewJob.na?digest=qT7i5B9ScgtZPY.MDlyPd6vJgKYK@D0vIx1XZPN8WiU\-&embedsource=Google","location":"BUFFALO","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do"}

Evaluates the chemical and physical properties of various organic and inorganic substances in order to meet customer requirements. Has knowledge of commonly-used analytical concepts, practices, and procedures within clasical wet chemistry. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Job functions does require some exercising of independent judgment. Typically reports to a supervisor or manager. Must have analytical chemistry skills (experience in wet chemical, organic, inorganic and classical chemistry) - Ability to balance chemical equations and perform chemical calculations, knowledge/operation of Karl Fischer, UV/VIZ and auto-titrators. R&D Lab develops fluorine containing molecules for foams and refrigeration production. Preference is for candidate to have 2+ years previous experience in an analytical lab. Qualifications Requires a bachelor's degree in chemistry and 2+ years of experience in lab analysis. Additional Information

Job Title: Technician, Quality Reports To: Manager, Quality Buffalo, NY FLSA Status: Non-Exempt Responsible for quality system processes designed to ensure continuous flow of incoming and outgoing materials consistent with established standards and regulations including FDA 21 CFR 820, ISO 13485, and appropriate EU regulations. Ensures compliance in QC areas including review and generation of information for incoming materials and product release. Ensures compliance in the areas of equipment qualification and calibration, supplier qualification and management, and document control as needed. Ensures continued improvement and compliance with relevant FDA, ISO 13485, and EU regulations by participating in audit responses, and deviation, nonconformance, complaint, and CAPA processes as necessary. Promotes and participate in training activities related to the quality management system and product quality, safety and efficacy. Key Responsibilities: Responsible for performing final QC checks on all outgoing product shipments, which includes reviewing and assuring accuracy of both documentation and product. Responsible for release of incoming materials, manufactured materials, and finished products according to written specifications. Assist with the maintenance of the equipment qualification and calibration program and upkeep of the equipment database. Assist the QA/QC Manager with review and filing of calibration certificates, out of tolerance reports, deviations, and SCARs as necessary. Assist with the development and implementation of company SOPs as assigned. Perform document control and training activities as assigned. Requires an ability to complete cGMP documentation accurately, in accordance with standard operating procedures, and in a timely manner. Requires an ability to work independently to accomplish given tasks within given timelines. Requires an ability to multitask and adjust to changing priorities. Must report any deviations or nonconformities immediately to a Manager or Director. Other duties as assigned. Education: Associate's Degree in related field or equivalent work experience Experience: 1 or more years of previous related experience Minimum Requirements/Qualifications: Good communication and organizational skills and ability to multitask. Prior experience with ISO 13485 and 21 CFR 820 a plus. Thrives in a fast-paced, collaborative environment, efficiently works under pressure, within deadlines or other time essential constraints Excellent communication skills, both written and verbal, to clearly and concisely communicate to all levels of the organization Strong work ethic and an ability to excel within a rapidly changing and growing organization Physical Requirements/Working Conditions: Control exposures to hazardous chemicals & other safety hazards such as: Carcinogens. Strong and obnoxious fumes. Sharp and dangerous blades and needles. Biohazard exposure to specimens. Compensation & Benefits: Salary Range: $22/hr-$24/hr, depending on location, experience, and qualifications. Benefits coverage begins day 1, including the following: Medical, Dental, Vision Insurance Disability Insurance Life Insurance 401(k) company match Paid Time Off (15 days annually) Paid Holiday time (10 company-designated days) Tuition Assistance Additional benefits available with company package This position has not been approved for Relocation Assistance. The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job. They are not an exhaustive list of all of the duties and responsibilities associated with it. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.