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Why work for Butterball? This is not just a job, it's a career! We take pride in our employees, and our employees take pride in being a valued team member at Butterball! Join us Today and enjoy these great perks! · Academic Tuition Reimbursement · Medical, Dental, & Vision Benefits · Employee Assistance Program · 401K · Responsibilities: Perform pre-operational inspections, complete sponges and swabs in the RTE environment. Perform HACCP record reviews and direct observations. Complete product cuttings. Assess, investigate, and correct issues. Product failure and FM investigations. Knowledge, Skills & Abilities Excellent attendance and work record Excellent communication skills Mathematical Skills Able to interact with all levels of Management Able to speak, read and write English Able to work independently with limited Supervision Knowledge of Workplace Safety Rules Performs checks of Product Quality against specifications Assures GMP, HACCP, and SOP's are in compliance Investigates issues related to Quality and Food Safety Collects Microbiological and Product samples for testing and evaluation Applies "Holds" to non-conforming products and materials Assures Food Safety, Regulatory and Company Compliance Understanding of the Process Assists with audits of the process, GMP's and Food Safety as well as Customer Audits Assists with Troubleshooting of Plant Quality problems as well as Sanitation issues and problems Assists with product improvement projects Education and Experience: High School Diploma or Equivalent We embrace equal opportunity employment. Butterball is committed to the fair and impartial treatment of all employees and applicants for employment without regard to gender, age, race, religion, color, national origin, physical or mental disability, military/veteran status, sexual orientation, gender identity and expression, genetic information, marital status, parental status, pregnancy, or any other status protected by law. We embrace equal opportunity employment. Butterball is committed to the fair and impartial treatment of all employees and applicants for employment without regard to gender, age, race, religion, color, national origin, physical or mental disability, military/veteran status, sexual orientation, gender identity and expression, genetic information, marital status, parental status, pregnancy, or any other status protected by law. This position is deemed Safety Sensitive for purposes of Butterball's Drug/Alcohol Screening & Testing Policy. Details will be provided to individuals who receive a conditional job offer, or upon request.

Air Liquide Electronics innovative electronic materials respond to increasingly challenging customer demands for improved mobility, connectivity, computing power and energy consumption. We offer ultra pure carrier gases, a wide range of specialty gases and advanced precursor molecules, enabling equipment for safe distribution, purification and on-line purity control. On site, manufacturers rely on our expertise in providing full management of these gases, advanced molecules and equipment and in helping to continuously improve production processes. How will you CONTRIBUTE and GROW? Air Liquide is Hiring for an Organic Laboratory Manager in Fremont, CA! At Air Liquide, we are committed to building a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world. We are looking for you! Pay: $130,000.00 - $140,000.00 Benefits: Air Liquide Benefit Offerings Work Schedule: Monday - Friday, 8:30 am to 5:30 pm. Some holiday and weekend coverage may be required. The Organic Lab in Fremont, CA, located in the San Francisco Bay Area/Silicon Valley, is a specialized facility focused on a wide range of analytical measurements. These include Quality Control/Assurance (QC/QA), Failure Analysis, and Research & Development (R&D) support. The lab utilizes various advanced techniques such as GC-TCD/GC-FID/GC-MS, IC, FTIR, Raman Spectroscopy, UV-Vis, TGA/DSC, ATD-GCMS, HPLC/HPLC-MS, and NMR. The selected candidate will lead a dynamic and fast-paced team of highly skilled technicians, chemists and scientists. Responsibilities Team Leadership and Management: Manage a team of lab technicians, chemists and scientists. Oversee performance management, employee coaching and development, and goal setting. Manage and approve timesheets and Paid Time Off (PTO) requests. Prioritize daily production activities and ensure adequate resources to meet customer requirements. Provide daily updates to the laboratory director. Operational Excellence and Quality Assurance: Ensure staff adherence to Standard Operating Procedures (SOPs) and manage change requests to keep SOPs current and accurate. Participate in the quality program, ensuring accurate evaluation, interpretation, and verification of data (samples, calibration, quality control) for analyses performed by the team. Ensure proper maintenance of the organic lab instrument fleet. Troubleshoot and apply analytical thinking to chemical analyses and processes. Support the lab with the procurement of consumables and spare parts. Implement and sustain the 6S program. Identify and implement continuous improvement initiatives, demonstrating a continuous improvement mindset. Training and Development: Ensure the team is adequately trained and qualifications and certifications are up to date. Maintain a cross-training plan based on a training gap analysis. Production and Support: Participate in production activities during team absences and periods of high capacity demand. Support various activities such as quality assurance, contamination studies, R&D, and failure analysis. _____________________ Are you a MATCH? Requirements B.S. in Chemistry or a related field with a minimum of 5 years of working experience with analytical instrumentation. Minimum of 5 years of supervisory/performance management experience in a laboratory environment. Considerable experience and knowledge in sample preparation and analysis of various sample types for analyses to determine results including purity/assay, organic impurities, surface organic contamination, and unknown identification utilizing instruments including, but not limited to GC/GC-MS, LC/LC-MS and FTIR. Adhere to and promote all safety protocols, ensure a safe working environment, and maintain up-to-date safety training for the team. Adapt to changing customer needs and priorities, and provide support to other laboratory areas as needed. Demonstrated understanding of a wide variety of analytical techniques and experimental design, particularly GC (coupled with TCD, FID, MSD), LC/LC-MS and FTIR analyses. Excellent proficiency in analytical instrumentation software, Microsoft Office Suite/Google Suite, and LIMS. Ability to work effectively in a team, with strong written and spoken communication skills. Self-motivated, proactive, organized, detail-oriented with good record-keeping skills, resourceful, and possesses strong problem-solving abilities. Ability to lift loads up to 35 lbs. and wear all required personal protective equipment. Candidates must have valid employment authorization in the U.S. and must not require visa sponsorship now or in the future. This position is not open for non-immigrant visa sponsorship.

Job Title: Associate Specialist, QC Duration: 23 Months Pay Rate: $31/hr on W2 Shift: Monday - Friday 10:00 AM to 6:00 PM EST Education/Experience Requirements • Associate's degree in Biology, Microbiology, Biochemistry, or related field plus 1-2 years of relevant laboratory/pharmaceutical experience • Bachelor's degree in Biology, Microbiology, Biochemistry, or related field Required Experience and Skills • Understanding and application of Good Laboratory Practices and cGMPs • Aseptic technique • Performance of environmental and water systems monitoring • Working in a team environment Preferred Experience and Skills • Strong verbal and written communication skills • Experience with LIMS, SAP or other laboratory/production software systems Working Relationships • Reports to Quality Control manager • Interacts with employees within own department and other departments Additional Information Our Quality group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe. The main function of the Associate Specialist, Quality Control is to assist in the assurance of the quality of product through the performance of microbiological, chemical and analytical sampling and assays as well as interacting with Production, Quality Assurance, Validation and Facilities, and external resources, as necessary to support Manufacturing. Responsibilities General • Conducts release testing in support of finished product • Conducts microbiological testing; evaluation of environmental microbiological samples • Conducts environmental monitoring sampling to include active air and surface sampling and water sampling • Evaluates data, conducts trouble shooting, process improvements, report writing, involvement in interdepartmental committees and projects • Maintains lab materials and reagents Business & Functional Expertise • Completes assignments in alignment with department objectives • Conducting In-Process and Release testing • Conducting Environmental Monitoring of processes and on a routine basis Problem Solving o Identifies and resolves technical and operational problems in collaboration with colleagues and under guidance from department head Impact Influence o Communicates information, asks questions and checks for understanding Accountability o Accountable for own performance Decision Making o Makes decisions - guided by policies and procedures - on the shop floor o Consults on an as-needed basis with next-level manager on more complex decisions and/or issues that impact other units with inter-related processes

* Travel: All expenses are paid by the company. What this Job Entails: The Field Technician III will provide support to all assigned locations, including data centers and Points of Presence (POPs), and physical site services. The person in this role will coordinate with network teams as well as local vendors for installation, repair and maintenance activities. The Field Technician must have deep knowledge and professional experience deploying (physical layer) rack and stack configurations. This role requires travel. Scope: Works on assignments that require considerable judgment and initiative. Makes recommendations for solutions Works within guidelines and takes ownership of results. May act as a mentor to less experienced team members Your Roles and Responsibilities: Maintain the highest quality standards in all assigned data center locations and remote points of presence (POP). Perform physical installation, repair, maintenance, and testing activities as directed with meticulous attention to driving and maintaining the highest quality standards in the telecommunications industry. Perform card adds or replacements, software upgrades, and associated testing. Recommend improvements to processes that may impact the quality of our network assets or improve overall efficiencies for any related process or system. Provide site survey support for OSP and ISP projects, as well as large space & power and/or equipment deployments. Perform site audits and reconcile data discrepancies in coordination with Network Surveillance and other groups as necessary. Manage local construction vendors working on behalf of the company to ensure compliance with installation, repair, maintenance MOPs and standards, as well as quality and cleanliness. Meet/coordinate with Local Exchange Carrier (LEC) and other technicians to facilitate timely installation, repair, and maintenance activities as necessary. Perform site surveys in support of network builds, augments, or decommissions. Coordinate site access, equipment staging, and other tasks Adeptly leverages knowledge and expertise Other duties as required. This list is not meant to be a comprehensive inventory of all responsibilities assigned to this position Required Qualifications/Skills: Associate's degree (A.A) or equivalent from two-year college or technical school and 5+ years' related experience and/or training; or equivalent combination of education and experience Networks with senior internal and external personnel in own area of expertise Demonstrates good judgment in selecting methods and techniques for obtaining solutions Experience working with data center and POP infrastructure, including experience or deep understanding of OSP, ISP, interfacility cabling, fiber and copper distribution, AC/DC power systems, environmental controls, and relay rack/cabinet/cage construction. Experience with installing and maintaining a wide variety of telecom/network equipment, including DWDMs, backbone and management routers, IP switches, as well as all optical and digital infrastructure. Deep understanding of splicing, and an understanding of how to maintain and operate within a manhole, vault, or handhole environment. Experience with telecommunications testing equipment from microscopes and source and power meters to OTDRs and experience testing across all SONET and Ethernet bandwidths. Extensive knowledge of telecommunications testing standards and procedures from length, wire-mapping, and bit error rate to power, delay, loss, reflectance and dispersion. Experience with state and local regulatory standards, procedures, and permitting requirements. Ability to work effectively with local exchange carrier (LEC) and other telecom service provider technicians, building landlords, electricians, construction operators, and non-technical end users. Ability to work independently, diagnose problems and take appropriate action with minimal supervision. Proficiency with spreadsheets, workflow and project management applications, and administrative software applications. Experience working with a Tier-1 ITSM platform

Job Posting Start Date 12-10-2025 Job Posting End DateFlex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary The Quality Lab Supervisor will be based in Buffalo Grove, IL reporting to the Quality Compliance manager. This role Supervises and coordinates activities related to the Quality Assurance Inspection function. Quarantine and disposition of nonconforming goods, while ensuring the policies and processes are followed. ROTATING 12 HOUR SHIFT/ NIGHT SHIFT/ B SHIFT, 6 PM - 6 AM What a typical day looks like: Support the site's Quality Compliance team to assure the conformance of all organization's regulatory and quality systems requirements. Perform internal audits and/or review results from Quality Compliance team to identify trends and opportunities for improvement. Verify compliance and conformance to all regulatory and quality systems requirements, including both Customer and Flex mandated. Engage in External Audit Processes (Customers', Regulatory, Government Agencies, etc.). Verify the proper implementation and effectiveness of the applicable Regulations, Standards, Policies, Directives and Level 1 Procedures in the organization. Provide support to any area that requires help to implement regulatory and quality requirements into their processes. Develop training programs for internal users in subjects related to Regulations or Quality Systems. Execute the formation of Regulatory and Quality Systems skilled employees that help support the organization. Develop Internal / External Audits Programs. Prepare the Audit Plan and related Audit Checklists. Execute Audits according to the plan, prepare the audit reports and maintain all audit related records. Plan, execute and follow up any Area/Process Audit when required by the organization. Create audit reports that identify any Non-Conformance or Opportunities for Improvement found during the audit process. Document all audit findings and request the corrective / preventive actions needed. Participate as a key member for all external audits activities and maintain records as required. Follow up on internal and external corrective actions to ensure timely implementation and validate their effectiveness. The experience we're looking to add to our team: Typically requires 5 years of related quality experience. Bachelors degree required with a preference to science related discipline at least 1 year as a lead or supervisor Must have Lab experience, Microbiology or other lab experience What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Pay Range (Applicable to Illinois)$60,400.00 USD - $83,000.00 USD AnnualJob CategoryQualityRelocation: Not eligible Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us. Click on the link below to learn what our employees have to say about Evonik: ************************************************** This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. Responsibilites: Has a sound understanding of the skills required to perform the following routine activities: Environmental Monitoring - Monitoring of Classified Areas using a) active/passive air sampling methods and RODAC/swab surface sampling methods for the detection of bacteria and fungi; and b) CliMet air sampling methods for the detection of Total Particulates; trending of this data to detect anomalies, and characterize the transient and resident microflora. Utilities -Testing of a) city water for total microbial count and the absence of enteric organisms; b) pre-treat water, clean steam and Water for Injection for total microbial count and presence of endotoxins; and c) nitrogen and process air for total microbial count and total particulates. Utilizes classical microbiological methods for the identification of microorganisms. Perform validation activities such as biological indictor recovery, bioburden rinse/swab, endotoxin rinse and endotoxin challenge vial testing. Data analysis and entry into software systems such as Microbiology Information Management Systems (MIMS). GMP Documentation - Document test results and conclusions in a GMP manner. Ensure test forms are complete before submission for approval. Performs responsibilities in compliance with Evonik quality systems. Adheres to all company safety, health and environmental policies, procedures and directives. Conducts all laboratory activities in a safe manner by use of MSDS to establish chemical hazards, observes the appropriate laboratory procedures and reports all incidents that could threaten the safety of laboratory personnel Requirements: Bachelor's degree in microbiology, biological sciences, or related field of study Minimum 1 yr. experience in a clinical, academic, or industrial/pharmaceutical microbiology laboratories. Experience in microbiological assays and testing. Desired experience in environmental monitoring and trending. Desired experience in the testing of utilities. Excellent written and verbal communication skills. Excellent organizational and leadership skills. Proficiency in Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMP). Excellent computer skills including experience with spreadsheets and databases. Ability to use a respirator. Ability to work with microorganisms and hot liquids. The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations. Your Application To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at *************************** Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Your Talent Acquisition Manager: Kelvin Seals [C] Company is Evonik Corporation

What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us. Click on the link below to learn what our employees have to say about Evonik: ************************************************** This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. Responsibilites: * Has a sound understanding of the skills required to perform the following routine activities: * Environmental Monitoring - Monitoring of Classified Areas using a) active/passive air sampling methods and RODAC/swab surface sampling methods for the detection of bacteria and fungi; and b) CliMet air sampling methods for the detection of Total Particulates; trending of this data to detect anomalies, and characterize the transient and resident microflora. * Utilities -Testing of a) city water for total microbial count and the absence of enteric organisms; b) pre-treat water, clean steam and Water for Injection for total microbial count and presence of endotoxins; and c) nitrogen and process air for total microbial count and total particulates. * Utilizes classical microbiological methods for the identification of microorganisms. * Perform validation activities such as biological indictor recovery, bioburden rinse/swab, endotoxin rinse and endotoxin challenge vial testing. * Data analysis and entry into software systems such as Microbiology Information Management Systems (MIMS). * GMP Documentation - Document test results and conclusions in a GMP manner. Ensure test forms are complete before submission for approval. * Performs responsibilities in compliance with Evonik quality systems. * Adheres to all company safety, health and environmental policies, procedures and directives. * Conducts all laboratory activities in a safe manner by use of MSDS to establish chemical hazards, observes the appropriate laboratory procedures and reports all incidents that could threaten the safety of laboratory personnel Requirements: * Bachelor's degree in microbiology, biological sciences, or related field of study * Minimum 1 yr. experience in a clinical, academic, or industrial/pharmaceutical microbiology laboratories. * Experience in microbiological assays and testing. * Desired experience in environmental monitoring and trending. * Desired experience in the testing of utilities. * Excellent written and verbal communication skills. * Excellent organizational and leadership skills. * Proficiency in Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMP). * Excellent computer skills including experience with spreadsheets and databases. * Ability to use a respirator. * Ability to work with microorganisms and hot liquids. The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations. Your Application To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at *************************** Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Your Talent Acquisition Manager: Kelvin Seals [C] Company is Evonik Corporation

Responsibilities Follows defined test plans and datasheets with necessary supervision/support. Evaluates test performance and sample operation to properly evaluate test results. Records and explains test results and completes test report. Serves as Lead for simple test programs as assigned with the necessary assistance. Communicates project status and results as needed. Holds responsibility for defining test plan, report completion and accuracy, meeting of agreed deadlines, and managing project related activities. Examines customer samples and learns to operate appropriate tests for each case with support. Communicates with internal customers during setup and operation to ensure proper evaluation. Directs, builds and/or adapts simple test setups, sample preparations/solutions and instruments to new situations, based on test plans and instructions. Trains other lab staff on these test procedures or instruments. Operates and maintains test instruments appropriately to measure and test samples. Performs maintenance on designated test instruments and laboratory area. For a single testing technology, integrates basic process and instruments improvements into all aspects of the job. Communicates with management and technical staff to provide suggestions for new instruments, processes, and forms to improve accuracy and efficiencies. Understands and follows safe chemical hygiene practices. Read and follow the Underwriters Laboratories Code of Conduct, and follow all physical and digital security practices. Other duties as assigned. #LI-BW1 #LI-Onsite Qualifications Bachelor's degree or diploma from an accredited university through a formal program of study in Chemistry or related discipline including Chemical Engineering, Biochemistry, Organic/Inorganic Chemistry, Material Science but not limited to these disciplines only. Demonstrated ability to manage multiple projects while maintaining high quality and exceptional customer service. Demonstrated ability to successfully partner with Engineering and other Laboratory Personnel to complete projects in a timely manner with high quality. Demonstrated ability to analyze special testing needs. Effective communication skills and ability to interact with customers Demonstrated ability to be innovative and creative Desire to work in a team-oriented environment Ability to use Microsoft Office suite is a must Ability to incorporate automation into day-to-day testing. Total Rewards: We understand compensation is an important factor as you consider the next step in your career . The estimated salary range for this position is $52,900 to $70,500 and is based on multiple factors, including job-related knowledge/skills, experience, geographical location, as well as other factors. This position is eligible for annual bonus compensation with a target payout of 5% of the base salary. This position also provides health benefits such as medical, dental and vision; wellness benefits such as mental and financial health; and retirement savings (401K) commensurate with the standard rewards offered in each individual location or country. We also provide full-time employees with paid time off including vacation (15 days), holiday including floating holidays (12 days) and sick time off (72 hours).

Who We Are FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Mesa, Arizona facility for a Development Lab Chemist! With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process. The Role Responsibilities include supporting pilot line builds for formulated products, executing formulated products build plans, generating test data, assisting maintaining lab and pilot line equipment including 4-point probe, ellipsometer, FTIR, back up SEM/FIB and XRR operator, general lab assistance where needed. Company Overview FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry-where chemistry meets technology. Our advanced materials and formulations enable manufacturers to build the microchips that power Artificial Intelligence, computers, electric vehicles, smartphones, and more. We're a global business-to-business supplier of chemical formulations and advanced materials used for manufacturing and packaging semiconductors. Our chemical formulations allow top manufacturers to produce microchips that both power and connect our digital world. Think you've got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what's possible-for the world and your future. We have six U.S. manufacturing and Research & Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island-each offering unique local experiences, from vibrant cultural scenes to historic charm. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Key responsibilities for this role include: * Assists in the design, development and commercialization of new post etch, post ash and post CMP cleaners and removers for advanced IC technologies. * Assists in mixing, filtering, and documentation of new speciality cleaners and etchants for semiconductors. * Assists with testing new cleaner formulations for shelf life and stability. * Back up SEM/FIB and XRR operator * Performs other duties as assigned by Wet Lab Supervisor * Specific activities include: * Investigate and develop new chemical formulations for cleaning integrated circuit wafers with awareness of the status of intellectual property field * Operating wet lab characterization tools * Coordinates with formulated products staff on chemistry and hardware supply needs * Chemical and wafer inventory tracking REQUIREMENTS * Bachelor's degree in chemistry or material science * 1 to 5 years of experience in a production lab environment * Experience in operating SEM/FIB equipment or desire to learn. * Person should be comfortable with dealing with and handling chemicals. * Experience in pilot line scale chemical manufacturing processes preferred. * Excellent communication, data collection, time management and organizational skills required. * Understand design of experiments and be proficient in technical writing. * Excellence in understanding and following instructions. * Must have excellent computer skills (Power-Point, Excel and statistical software tools). * Working knowledge of JMP statistical software is desirable. * This is a safety-sensitive position that requires candidates to successfully pass a post-offer drug screening prior to employment. One of the essential job functions is the ability to work in a constant state of alertness and in a safe manner. ADDITIONAL REQUIREMENTS We value a professional, adaptable, and collaborative work environment. The following competencies are essential for success in any role and reflect our commitment to effective teamwork, problem solving, and workplace communication. * Resilience -Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively. * Communication -Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships. * Reasoning & Decision Making -Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions. * Comprehension -Capability to understand and complete tasks as assigned and solve problems effectively. * Organizational Skills -Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions. To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (********************************).

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for formulation of powdered media. 3rd Shift: 9:00 pm- 5:30 am At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Responsibilities: * Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. * Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. * Suggest changes in departmental procedures and processes (SOPs) as needed. * Performs and documents line clearance at the start of each formulation event. * Maintains all required logs and associated documentation. * Assures that all chemicals are stored and labeled properly. * Performs process scale checks on all required equipment including scales and balances. * Keeps work area, utensils, tanks, mills, and equipment clean and organized. * Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. * Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. * Understands and follows procedures to ensure that chemicals are handled properly. * Good understanding of metric system and its conversions. * Follows and actively participates in sustaining the 6S program in the area. * Other duties as requested by Lead or Supervisor. Required Skills/Education: * High School Diploma or equivalent. * Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. * 1-2 years of hands on experience * General education about chemicals and proper handling (college level science preferred). * Working knowledge of metric system. * Good understanding of current Good Manufacturing Practices (cGMPs). * Ability to speak, read, and write English. * Good oral and written communication skills. Salary and Benefits: * For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). * Medical, Dental, Vision * Life Insurance * 401k * Paid Time Off * #LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

McCormick & Company, Inc., a global leader in the spice, flavor, and seasonings industry, is seeking a full-time Analytical Lab Technician I. This new hire will work at the Flavor Manufacturing Center in Hunt Valley, MD. The Analytical Lab Technician I will report to a QA Team Manager. What We Bring to The Table: The best people deserve the best rewards. In addition to the benefits you would expect from a global leader (401k, health insurance, paid time off, etc.), we also offer: Competitive compensation Career growth opportunities Flexibility and Support for Diverse Life Stages and Choices We prioritize our communities and the planet we share. We are proud to be awarded as a Diversity Inc. Top 50 company for Diversity and have multiple Sustainability awards (ranking #22 in the World and #1 in Food Products) Wellbeing programs, including Physical, Mental, and financial wellness Tuition assistance POSITION OVERVIEW Under the general direction of the quality manager, the qualified candidate will be responsible for performing analytical tests, including chemical and physical tests in addition to sensory tests, which are required for quality control of raw materials, in-process materials, and finished goods. Participates in investigations and studies to determine cause, effect, and corrective actions required to resolve deviation from quality standards-routine sampling and inspection of material. The employee will adhere to safety procedures, ensure a safe work environment, meet and exceed product quality expectations, and assist in achieving process reliability goals. RESPONSIBILITIES: Performs analytical testing using a variety of test methods, procedures, and instrumentation and records, maintains, and reviews results/data in SAP System Performs sensory tests and participates in sensory-related tasks Required to calibrate, maintain, and troubleshoot laboratory equipment as needed Initiates & documents Quality Notifications/DMRs/DMAs, including participating in cross-functional root cause analysis. Facilitates follow-ups & resolutions Interprets data and gives direction to the manufacturing group to ensure products meet established specifications. Prepares samples of raw materials, intermediates, and finished goods to be sent out for outside testing, including environmental testing Performs COA verification and raw material sampling Audits various operational activities as assigned Supports quality projects as required REQUIRED QUALIFICATIONS: HS diploma or GED Minimum of 1-2 years of related experience (manufacturing experience is acceptable). Knowledge of Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs). Knowledge of PC software and data entry experience Ability to work well under pressure while maintaining multiple priorities; ability to work with minimal supervision. Excellent written and oral communication skills Color Vision (ability to detect color) required. This is due to the need to compare color differences in products daily Must occasionally wear a PAPR to perform necessary duties on the production floor. PREFERRED QUALIFICATIONS: A four-year college degree in science (food science, chemistry, etc.) or a two-year science diploma and two years of relevant technical experience or five years of relevant technical experience. Experience working in food manufacturing Working knowledge of statistics preferred McCormick & Company is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. As a general policy, McCormick does not offer employment visa sponsorships upon hire or in the future.

McCormick & Company, Inc., a global leader in the spice, flavor, and seasonings industry, is seeking a full-time Analytical Lab Technician I. This new hire will work at the Flavor Manufacturing Center in Hunt Valley, MD. The Analytical Lab Technician I will report to a QA Team Manager. What We Bring to The Table: The best people deserve the best rewards. In addition to the benefits you would expect from a global leader (401k, health insurance, paid time off, etc.), we also offer: Competitive compensation Career growth opportunities Flexibility and Support for Diverse Life Stages and Choices We prioritize our communities and the planet we share. We are proud to be awarded as a Diversity Inc. Top 50 company for Diversity and have multiple Sustainability awards (ranking #22 in the World and #1 in Food Products) Wellbeing programs, including Physical, Mental, and financial wellness Tuition assistance As a company recognized for its exceptional commitment to employees, McCormick offers a wide variety of benefits, programs, and services. Benefits include but are not limited to tuition assistance, medical, dental, vision, disability, group life insurance, 401(k), profit sharing, paid holidays, and vacations. POSITION OVERVIEW Under the general direction of the quality manager, the qualified candidate will be responsible for performing analytical tests, including chemical and physical tests in addition to sensory tests, which are required for quality control of raw materials, in-process materials, and finished goods. Participates in investigations and studies to determine cause, effect, and corrective actions required to resolve deviation from quality standards-routine sampling and inspection of material. The employee will adhere to safety procedures, ensure a safe work environment, meet and exceed product quality expectations, and assist in achieving process reliability goals. RESPONSIBILITIES: Performs analytical testing using a variety of test methods, procedures, and instrumentation and records, maintains, and reviews results/data in SAP System Performs sensory tests and participates in sensory-related tasks Required to calibrate, maintain, and troubleshoot laboratory equipment as needed Initiates & documents Quality Notifications/DMRs/DMAs, including participating in cross-functional root cause analysis. Facilitates follow-ups & resolutions Interprets data and gives direction to the manufacturing group to ensure products meet established specifications. Prepares samples of raw materials, intermediates, and finished goods to be sent out for outside testing, including environmental testing Performs COA verification and raw material sampling Audits various operational activities as assigned Supports quality projects as required REQUIRED QUALIFICATIONS: HS diploma or GED Minimum of 1-2 years of related experience (manufacturing experience is acceptable). Knowledge of Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs). Knowledge of PC software and data entry experience Ability to work well under pressure while maintaining multiple priorities; ability to work with minimal supervision. Excellent written and oral communication skills Color Vision (ability to detect color) required. This is due to the need to compare color differences in products daily Must occasionally wear a PAPR to perform necessary duties on the production floor. PREFERRED QUALIFICATIONS: A four-year college degree in science (food science, chemistry, etc.) or a two-year science diploma and two years of relevant technical experience or five years of relevant technical experience. Experience working in food manufacturing Working knowledge of statistics preferred McCormick & Company is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. As a general policy, McCormick does not offer employment visa sponsorships upon hire or in the future.

Pangea Laboratory seeks a dynamic individual to become an integral part of our Laboratory Operations team! In this role, you will assist with specimen processing and test performance while complying with all regulatory agency guidelines. This role requires knowledge of laboratory procedures, strong attention to detail, and the ability to work effectively both independently and as part of a team. The successful candidate must also adhere to all laboratory health and safety regulations. This position is Monday-Friday from 10:30AM to 7PM onsite in Tustin, CA. Join us in making a meaningful impact! Essential Duties and Responsibilities: Comply with all policies and regulations put in place by Pangea Laboratory, State, Federal, CAP, CLIA, and HIPAA. Complete routine handling, accessioning, and storage of laboratory specimens in accordance with standard operating procedure. Document laboratory information using appropriate information management systems and verify information and discrepancies. Identify and troubleshoot problems in a timely manner and adhere to laboratory procedures when resolving problems. Direct handling of potential hazardous specimens and reagents under safe environment while wearing appropriate PPE. Be familiar with laboratory protocols and procedures for specimen processing, operating equipment and instruments, maintenance of designated laboratory environment and instruments, and data entry. Label and store working reagents and solutions in accordance with standard operating procedure and safety guidelines. Adequately communicate information with team members and management relating to laboratory procedures, equipment, information, issues, etc. Handle light logistical duties, including coordinating the shipping of materials and samples to ensure timely delivery. Ensure testing turnaround time by closely monitoring specimens received and pending processing. Document records in real time using good documentation practices that include but is not limited to department forms, files, and worksheets. Meet or exceed all performance expectations and demonstrate professional working behavior when performing tasks and interacting with team members. Adapt to changes in processes, accepting approved changes and learning new tasks. Follow Pangea Laboratory health and safety policies and procedures and are responsible for reporting violations. Perform other related duties as required or assigned. Education and Experience: 1 year experience in research in the biotech/life sciences industry, or an equivalent combination of education, training, and experience. A Bachelor's or Associate degree in a relevant scientific field (Biology, Chemistry, or a related discipline). General Skills: Have background or basic knowledge in laboratory procedures and guidelines. Have the ability to read, write (legibly), and speak the English language. Strong attention to detail, excellent organizational and time-management skills. Have the ability to quickly understand procedures and be flexible to changes and updates in procedures. Have the ability to troubleshoot and recognize abnormalities then demonstrate proactiveness to address issues in the workflow. Demonstrate autonomy and possess time management skills. Demonstrate ability to prioritize tasks and engage in multi-tasking without sacrificing quality. Computer Skills: Knowledge of basic computer skills such as Microsoft Office Suite to include Excel and Word. Previous experience with Laboratory Information Management Systems, preferred. About Us: Pangea Laboratory is a California-based diagnostics company founded in 2014. We focus on the precise, early detection of emerging diseases. Our mission is to have a positive impact on human life, by providing biomedical communities with reliable and high-quality testing services, delivering the data they need to diagnose and treat diseases in an effective and timely manner. Named a Top Workplace by the OC Register, Pangea Laboratory continues to be a place where employees feel engaged, connected, and energized about their work. If you are passionate about helping people in advancing science and working with awesome teams in a fast-growing company, we want to speak with you! Compensation: The estimated base compensation range for this position is $24 to $28 per hour at the time of posting. Actual compensation details will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. Equal Employment Opportunity Employer: Pangea Laboratory welcomes candidates of all backgrounds. These include sex, age, color, race, religion, marital status, national origin, ancestry, sexual orientation, gender, gender identity, gender expression, physical & mental disability, medical condition, genetic information, military and veteran status, or any other protected status as defined by federal, state, or local law. Location: Onsite - Pangea HQ - 14762 Bentley Cir. Tustin, CA 92780

Requirements · Operate, calibrate, and maintain laboratory equipment to include Foss FTIR, Brix, pH meter, EQA, CEM, scales, and pipettes. · Perform organoleptic testing on required product samples including fresh and at code products · Perform accurate physiochemical and microbiological preparation, testing, counting and examinations of raw materials, in process products, and finished goods. · Approve release of in process and finished products including "first off" testing, while verifying adherence to stated specification. · Record and enters data, creates COA's, and other reports, promptly and accurately. · Maintain various production, raw material, testing, and quality control records in an organized manner. · Report and take necessary action to prevent food safety and food quality issues from occurring. · Perform pre-operational checks and sanitation inspections in adherence to filler release procedure. · Perform environmental swabbing, line checks, allergen tests, special projects, and any other duties as assigned. · Apply proper aseptic sample collection, transport, storage testing, and disposal. · Follow all company Safety Policies, Good Lab Practices, Good Manufacturing Practices, and Standard Operating Procedures. · Proficient in the use of standard computer software, i.e. Microsoft Outlook, Word, Excel, PowerPoint. · Excellent written and verbal communication skills · Knowledge of US customary units and metric system including weights and measures. POSITION REQUIREMENTS: · Bachelor's Degree in Food Science, Microbiology, Biology or related field or 2 years experience. Crystal Creamery is an Equal Opportunity Employer and does not discriminate any employee or applicant because of race, color, religion, national origin, ancestry, marital or veteran status, disability, medical condition, sex, or age (as defined by applicable law). Any offer of employment by Crystal Creamery may be contingent upon passing a background check, medical examination and or drug test. To apply please visit *********************** click on careers and job openings. Salary Description 23.00 to 27.60 DOE

Crystal Creamery is currently looking for Lab Technician for our Dairy Manufacturing Plant in Modesto. The Lab Technician with general direction shall perform routine laboratory and administrative duties, assist other lab members professionally and respectfully, keep accurate and legible records, have the ability to prioritize work assignments effectively, in addition to reviewing work for quality and completeness. The Lab Technician will also safely operate testing equipment involving potential chemical and temperature hazards, accurately identify and restock lab supplies to maintain a current lab supply and inventory rotation, prepare samples, media and solutions for testing, high acceptance of performing other related duties and projects as assigned. Requirements Job Duties: * Operate, calibrate, and maintain laboratory equipment to include Foss FTIR, Brix, pH meter, EQA, CEM, scales, and pipettes. * Perform organoleptic testing on required product samples including fresh and at code products * Perform accurate physiochemical and microbiological preparation, testing, counting and examinations of raw materials, in process products, and finished goods. * Approve release of in process and finished products including "first off" testing, while verifying adherence to stated specification. * Record and enters data, creates COA's, and other reports, promptly and accurately. * Maintain various production, raw material, testing, and quality control records in an organized manner. * Report and take necessary action to prevent food safety and food quality issues from occurring. * Perform pre-operational checks and sanitation inspections in adherence to filler release procedure. * Perform environmental swabbing, line checks, allergen tests, special projects, and any other duties as assigned. * Apply proper aseptic sample collection, transport, storage testing, and disposal. * Follow all company Safety Policies, Good Lab Practices, Good Manufacturing Practices, and Standard Operating Procedures. * Proficient in the use of standard computer software, i.e. Microsoft Outlook, Word, Excel, PowerPoint. * Excellent written and verbal communication skills * Knowledge of US customary units and metric system including weights and measures. POSITION REQUIREMENTS: * Bachelor's Degree in Food Science, Microbiology, Biology or related field or 2 years experience. Crystal Creamery is an Equal Opportunity Employer and does not discriminate any employee or applicant because of race, color, religion, national origin, ancestry, marital or veteran status, disability, medical condition, sex, or age (as defined by applicable law). Any offer of employment by Crystal Creamery may be contingent upon passing a background check, medical examination and or drug test. To apply please visit *********************** click on careers and job openings.

Performs a variety of duties involving laboratory testing of prototypes in the process of research and development, to determine the acceptable standards of performance theoretically established by engineering. Sets up, arranges and operates mechanical or electrical test equipment in the proper test sequences. Tests prototype and records test data for analysis and evaluation by engineers. When directed, tests competitive products or spot tests manufactured products or components for quality control purposes. Major Responsibilities: Mounts and secures test samples and operates test devices through prescribed sequences; a Lab Tech checks the set ups and reviews the test results Setup mechanical and/or electrical testing devices and apparatus according to test specifications Reads and records test data and calls attention to deviations or variations not indicated or anticipated Makes setups, performs test assignments, and completes data sheets in neat, accurate and timely fashion to meet needs of test schedule Interface directly with engineering staff for assigned tasks related to test, inspection, tear-down, and reporting technical information Disassemble electric motors and generators for test and evaluation as well as reassemble back to salable condition Complete maintenance and housekeeping for assigned equipment and work spaces Take active role in defining and implementing personal and departmental continuous improvement Required Education / Experience / Skills: Requires completion of a 2 year technical degree program or similar electrical experience. Must be able to read and interpret mechanical and electrical engineering drawings Must have safe working experience with AC & DC electrical systems. NEC & NFPA code experience desired. Experience with tools and instruments related to installation and testing for electric motors, generators, and drives preferred. Written communication skills using Microsoft Office (Outlook, Excel, Word) applications to clearly exchange technical information and concepts is desirable. Experience reviewing, creating, or editing CAD documents using DraftSight or Solidworks software is desirable. Founded in 1961, WEG is a global electric-electronic equipment company, operating mainly in the capital goods sector with solutions in electric machines, automation and paints for several sectors, including infrastructure, steel, pulp and paper, oil and gas, mining, among many others. WEG stands out in innovation by constantly developing solutions to meet the major trends in energy efficiency, renewable energy and electric mobility. With manufacturing units in 17 countries and present in more than 135 countries, the company has more than 45,000 employees worldwide. WEG's net revenue reached R$ 32.5 billion in 2023, 52.9% from outside Brazil. Our business areas are divided as follows. Industrial Electro-Electronic Equipment This area includes electric motors, drives and industrial automation equipment and services, and maintenance services. Electric motors and other related equipment find applications in practically all industrial segments, in equipment such as compressors, pumps and fans, for example. Energy Generation, Transmission and Distribution (GTD) Products and services included in this area are electric generators for hydraulic and thermal power plants (biomass), hydro turbines (small hydroelectric plants or PCH, and hydroelectric generators or CGH)), wind turbines, transformers, substations, control panels and system integration services. Commercial and Appliance Motors In this business area, our focus is the market of single phase motors for durable consumer goods, such as washing machines, air conditioners, water pumps, among others. Paints and Varnishes In this area, which includes liquid paints, powder paints, and electro-insulating varnishes, we have a very clear focus on industrial applications in Brazil and are expanding to Latin America and other regions.

Performs a variety of duties involving laboratory testing of prototypes in the process of research and development, to determine the acceptable standards of performance theoretically established by engineering. Sets up, arranges and operates mechanical or electrical test equipment in the proper test sequences. Tests prototype and records test data for analysis and evaluation by engineers. When directed, tests competitive products or spot tests manufactured products or components for quality control purposes. Major Responsibilities: * Mounts and secures test samples and operates test devices through prescribed sequences; a Lab Tech checks the set ups and reviews the test results * Setup mechanical and/or electrical testing devices and apparatus according to test specifications * Reads and records test data and calls attention to deviations or variations not indicated or anticipated * Makes setups, performs test assignments, and completes data sheets in neat, accurate and timely fashion to meet needs of test schedule * Interface directly with engineering staff for assigned tasks related to test, inspection, tear-down, and reporting technical information * Disassemble electric motors and generators for test and evaluation as well as reassemble back to salable condition * Complete maintenance and housekeeping for assigned equipment and work spaces * Take active role in defining and implementing personal and departmental continuous improvement Required Education / Experience / Skills: * Requires completion of a 2 year technical degree program or similar electrical experience. * Must be able to read and interpret mechanical and electrical engineering drawings * Must have safe working experience with AC & DC electrical systems. NEC & NFPA code experience desired. * Experience with tools and instruments related to installation and testing for electric motors, generators, and drives preferred. * Written communication skills using Microsoft Office (Outlook, Excel, Word) applications to clearly exchange technical information and concepts is desirable. * Experience reviewing, creating, or editing CAD documents using DraftSight or Solidworks software is desirable. Founded in 1961, WEG is a global electric-electronic equipment company, operating mainly in the capital goods sector with solutions in electric machines, automation and paints for several sectors, including infrastructure, steel, pulp and paper, oil and gas, mining, among many others. WEG stands out in innovation by constantly developing solutions to meet the major trends in energy efficiency, renewable energy and electric mobility. With manufacturing units in 17 countries and present in more than 135 countries, the company has more than 45,000 employees worldwide. WEG's net revenue reached R$ 32.5 billion in 2023, 52.9% from outside Brazil. Our business areas are divided as follows. Industrial Electro-Electronic Equipment This area includes electric motors, drives and industrial automation equipment and services, and maintenance services. Electric motors and other related equipment find applications in practically all industrial segments, in equipment such as compressors, pumps and fans, for example. Energy Generation, Transmission and Distribution (GTD) Products and services included in this area are electric generators for hydraulic and thermal power plants (biomass), hydro turbines (small hydroelectric plants or PCH, and hydroelectric generators or CGH)), wind turbines, transformers, substations, control panels and system integration services. Commercial and Appliance Motors In this business area, our focus is the market of single phase motors for durable consumer goods, such as washing machines, air conditioners, water pumps, among others. Paints and Varnishes In this area, which includes liquid paints, powder paints, and electro-insulating varnishes, we have a very clear focus on industrial applications in Brazil and are expanding to Latin America and other regions.

Dental Lab Production Technician About Osteoid Inc. Osteoid is creating the next generation of seamless and connected 3D dental imaging software and solutions that help accelerate the path to digital dentistry. Proven in over ten years of use by thousands of labs and dental practices, Osteoid's software and hardware tools keep dental practices and labs ahead of the curve and allow dentists to competently diagnose any patient scan in 3D. An osteoid is a soft organic element that forms bones in the human body. Just like osteoids in the human body, Osteoid is providing the essential software to dental practice success. Osteoid is a wholly owned dental-focused subsidiary of Anatomage. ******************* About the Role As a Lab Production Technician at Osteoid, you will be working in a dental lab that produces custom medical devices used in dental implant procedures by utilizing 3D printing technology and dental lab equipment. Osteoid is growing at a rapid pace and we need Lab Production Technicians to help support the increasing client demand for our custom made products. This person will be an integral part of this team, working onsite in our dental lab to fabricate surgical guides for our dental clients. The ideal candidate has a dental background or previous lab experience. This person must have strong attention to detail, be comfortable working with small tools, and enjoy working in a fast-paced department. This is the perfect opportunity for someone looking to delve into 3D dental technology and be part of an exciting team. This role is $21/hr. What You'll Do Manufacture custom medical devices using a rotary tool Work alongside team members who support our dental clients with custom needs Process the 3D printed dental models once they are printed so they are prepared to be fabricated into medical devices Perform quality inspection of custom made medical devices Create digital images of orthodontic study models by using optical 3D scanning technology Monitor and maintain inventory levels Maintain an organized and safe work environment Perform maintenance of laboratory equipment Miscellaneous lab support duties as needed Requirements Skills and Abilities Required Manual dexterity and spatial awareness Strong attention to detail Comfortable working with small power tools Strong documentation skills Ability to work efficiently and effectively with moderate supervision Patience for repetitive tasks Ability to work closely with others and share equally in the workload Ability to manage and prioritize multiple tasks with competing demands Qualities We Look For Experience working in a dental office or laboratory Experience with Dremel style tools Experience with 3D software/printers Artistic/crafting background or interest Minimum Education and Experience Required High School Diploma or GED equivalent 1+ year of full time work experience Physical Requirements Standing, walking, sitting, reaching with hands and arms, grasping and feeling with fingers and palm, talking, hearing, and performing repetitive motions Ability to push, pull, lift, and/or carry up to 20 pounds Strong fine motor skills and good manual dexterity Ability to utilize close visual acuity to perform visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication parts at distances close to the eyes Benefits What We Offer Health, Dental, and Vision care for you and your family 401K savings plan with employer matching Generous PTO leave and paid holidays Casual work culture Commuter benefits Employee Assistance Plan Team bonding activities, catered lunches, free snacks and more! Additional Information about Osteoiod Anatomage Announces Osteoid Dental Subsidiary Anatomage Spins Out its 3D Dental Technology Business As Osteoid Anatomage Spins Out its 3D Dental Technology Business As Osteoid (different from 2nd link)

Dental Lab Production Technician About Osteoid Inc. Osteoid is creating the next generation of seamless and connected 3D dental imaging software and solutions that help accelerate the path to digital dentistry. Proven in over ten years of use by thousands of labs and dental practices, Osteoid's software and hardware tools keep dental practices and labs ahead of the curve and allow dentists to competently diagnose any patient scan in 3D. An osteoid is a soft organic element that forms bones in the human body. Just like osteoids in the human body, Osteoid is providing the essential software to dental practice success. Osteoid is a wholly owned dental-focused subsidiary of Anatomage. ******************* About the Role As a Lab Production Technician at Osteoid, you will be working in a dental lab that produces custom medical devices used in dental implant procedures by utilizing 3D printing technology and dental lab equipment. Osteoid is growing at a rapid pace and we need Lab Production Technicians to help support the increasing client demand for our custom made products. This person will be an integral part of this team, working onsite in our dental lab to fabricate surgical guides for our dental clients. The ideal candidate has a dental background or previous lab experience. This person must have strong attention to detail, be comfortable working with small tools, and enjoy working in a fast-paced department. This is the perfect opportunity for someone looking to delve into 3D dental technology and be part of an exciting team. This role is $21/hr. What You'll Do * Manufacture custom medical devices using a rotary tool * Work alongside team members who support our dental clients with custom needs * Process the 3D printed dental models once they are printed so they are prepared to be fabricated into medical devices * Perform quality inspection of custom made medical devices * Create digital images of orthodontic study models by using optical 3D scanning technology * Monitor and maintain inventory levels * Maintain an organized and safe work environment * Perform maintenance of laboratory equipment * Miscellaneous lab support duties as needed