Quality control analyst jobs in Ocala, FL - 30 jobs

📌 Quality Control Inspector 📍KeyStone Heights, FL 💰 Compensation: $38-45/hr (1.5× over 40 hrs, 2× over 50 hrs) 🚀 Why This Role Matters This position is essential to ensuring that all welds, materials, and fabricated components meet strict codes and quality standards. By maintaining compliance, supporting production teams in real time, and reinforcing quality processes, you'll help drive reliability, safety, and precision across high-tonnage fabrication operations. 🎯 Key Responsibilities Perform visual inspections, dimensional checks, layout verification, and welding parameter monitoring Maintain QC documentation, logs, and inspection records Support welder qualification testing and coordinate QC hold points Conduct bolt rotational capacity tests and assist with Total Station measurements Collaborate closely with welders, lead personnel, production teams, shipping, and external inspectors Communicate real-time quality decisions to keep production accurate and compliant ✅ Ideal Candidate Profile Required: Current CWI or ASNT VT Level II certification Strong blueprint reading and knowledge of welding codes Proficient with measurement tools and visual inspection techniques Detail-oriented, safety-focused, and strong communicator Preferred: ASNT MT Level II, UT Level II, NACE/SSPC BCI Level I, or heavy fabrication shop experience Submit resume to ************************** or apply online.

About AEL: Advanced Environmental Laboratories, Inc. (AEL) is Florida's largest environmental, chemical, analytical testing laboratory network. AEL has been in business for over 30 years and is a leader in the industry with modern instrumentation, computer technology, and opportunities of growth for our employees. Are you passionate about the environment? Join AEL! We are currently looking for senior and mid-level analysts for our AEL Gainesville, FL laboratory. This hire will join our growing team to support our mission of delivery high quality environmental data for our clients across Florida. Pay and Benefits: This is a full-time position with benefits including Health/Dental/Vision Insurance (60% paid by AEL), Floating Holiday, PTO, short and long term disability + life term insurance paid by AEL, and 401K retirement plan with up to 4% Company match. Salary based on experience. Job Description: Senior Analyst will be responsible for analyzing samples using manual and more complex instrumental and reporting techniques in accordance with prescribed methods, standard operating procedures, regulatory agency standards as well as client specifications. Aids in method development of new analyses and works on special projects as they arise. Provides extensive guidance for lower level analysts. Minimum Qualifications: Education: BS in Chemistry, Biology, Environmental Science, or equivalent Experience: 2 or more years as Analyst II or 5 years experience at another analytical laboratory High level reporting skills, Advanced instrument care and maintenance Ability to train others Continued Technical Skills, Knowledge, and Abilities: Analyze samples consisting of soil and water matrices using traditional laboratory technologies. Prepare samples for analysis while displaying good laboratory technique to avoid cross-contamination or misidentified samples. Accurately prepare calibration curves and quality control samples. Interpret and evaluate data in terms of accuracy, precision, trends, and quality control requirements. Maintain laboratory equipment by cleaning, and otherwise ensuring ongoing proper working order. Report equipment issues to Department Manager. Collaborate with the laboratory team to meet reporting deadlines. Ability to perform method validations, or verifications as needed. Manage inventory supplies and alert supervisor in advance when materials must be ordered May participate in root cause analysis for quality assurance. Assist with training, scheduling and supervision of lower level analysts and technicians on instrumentation and methodology. Participate in the development and updating of departmental SOPs. Other duties and special projects as assigned. Duties and Responsibilities: Adhere to Laboratory Standard Operation Procedures (SOPs), EPA methods, and Standard Methods Perform all duties associated with sample analysis of more complex laboratory tests. Analyze, interpret and review sample results, as well as, peer review of departmental data. Perform all quality control requirements associated with the methods and maintain appropriate records. Perform all work within established quality control parameters and within specified turnaround times. Troubleshoot and fix instruments as needed. Maintain high productivity, keen attention to detail, and consistent multi-tasking while yielding a low testing error rate. Strong agility, engagement, and flexibility in an ever-changing environment. Diligent commitment to organizing, analyzing and reporting data. Excellent communication skills and ability to effectively work, problem solve, and communicate with multiple levels of the organization. Provide department managers daily status information May be assigned duties to help manage Health and Safety and/or Hazardous Waste program

Kincell Bio engineers cells into therapies . With manufacturing facilities located in Research Triangle Park, NC and Gainesville, FL, Kincell Bio is a contract development and manufacturing organization (CDMO) with the mission to streamline CMC development, apply expertise in analytical and process development and GMP manufacturing, testing and release from early clinical to pivotal studies and product launch. Kincell Bio is focused on supporting innovative companies developing immune cell therapies, including autologous and allogeneic CAR-T, TCR, TILs, Tregs and CAR-NK technologies. We offer challenging career opportunities, competitive benefits, and an environment that recognizes and rewards performance. For more information, please visit our website at ******************* Kincell is seeking a highly motivated QC Analyst III who will be a key contributor to a dynamic and collaborative Quality Control team. The Quality Control Analyst III will primarily be responsible for supporting and leading early/late phase and commercial quality control activities. This highly motivated member of the Quality Unit will support the organization through the execution of activities such as raw material testing, release testing, stability testing, and environmental monitoring. This Quality team member will be responsible for initiating and assisting in investigations and troubleshooting while adhering to cGMP and GDP practices. Essential Duties and Responsibilities Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. This list contains the major duties and requirements of the job and is not all-inclusive. Incumbent(s) may be expected to perform role-related duties other than those contained in this document. Essential Duties and Responsibilities Actively participate in fostering a positive, collaborative work culture. Author and revise standard operating procedures, test methods, protocols, and reports. Lead in execution of raw material testing, stability testing, environmental monitoring, critical utility monitoring, method qualifications, technical transfers, release testing, and method validations. Assist in the transfer of assays from the Analytical Development Lab to the QC Lab. Demonstrate proficiency in flow cytometry, automated cell counting, dPCR, qPCR, ELISA-based, multiplex cytokine detection, pH, endotoxin, and cell-based assays. Ensure QC deliverables are met in a timely manner. Perform data analysis and review. Initiate and participate in laboratory investigations including deviations and out of specifications. Perform equipment calibrations. Execute method and equipment troubleshooting and optimization, as needed. Maintain documentation in accordance with GDP. Train and cross train QC personnel on standard operating lab procedures and test methods. Qualifications The requirements listed below are representative of the knowledge, skill, and/or ability required to perform this job successfully. Required: B.S. degree in science or a life science-related field of study 4+ years' experience in Quality Control in a GMP environment Proficiency in eukaryotic cell culture, molecular techniques, operation of microscopes, and equipment calibrations (e.g., pH meters and balances) Strong technical laboratory skills (e.g., pipetting, weighing, and measuring pH) Experience with writing standard operating procedures An equivalent combination of education and experience may be considered. Familiarity with FDA, ICH, and EU Regulations and Guidelines Involvement in continuous improvement initiatives and laboratory investigations Proficiency in Microsoft Office suite applications Excellent attention to detail, organizational skills, and ability to multi-task in a dynamic environment. Preferred: 4+ years' experience in Quality Control in a GMP environment, preferably with experience in a microbiology laboratory Experience with the following instrumentation: flow cytometers, qPCR, digital PCR, multimode plate readers Travel Requirements None. Location This is a 100% site-based position located at the Gainesville, FL site This position requires some non-standard working hours, including early morning or late evening. #LI-Onsite Kincell Bio provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, genetic information, marital status, amnesty, or status as a covered veteran in accordance with applicable, federal, state, and local laws. Kincell Bio complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. NOTE TO EMPLOYMENT AGENCIES: Kincell Bio values our relationships with our Recruitment Partners. We will only accept resumes from those partners who have been contracted by a member of our Human Resources team to collaborate with us. We are not responsible for any fees related to resumes that are unsolicited or are received without contract.

Bureau of Water Resource Information This is advanced professional work involving the performance and coordination of routine and complex laboratory analysis and equipment maintenance, coordinates with other Chemists in the design, development, and evaluation of new District analytical methods, coordinates the work of lower-level staff. May also function as a Project Manager for outsourced analysis, supplies and services. Job duties include: Performs advanced, complex laboratory analysis. Performs instrument installation and setup: install laboratory instruments in accordance with manufacturer specifications and facility requirements (e.g., electrical, ventilation, gas supply, bench space); ensure all necessary supplies and accessories are available for installation and start-up; document installation procedures and maintain records for audit purposes. Perform method development and validation: develop, optimize, and validate analytical methods for new and existing instruments; perform quality assurance testing, including analysis of check standards and proficiency testing samples; determine and verify method detection limits (MDL) and demonstrate capability according to established protocols; prepare and revise Standard Operating Procedures (SOPs) for instrument operation and method implementation. Perform training and support: Provide onsite training and user familiarization for lab staff during and after instrument installation; serve as a technical resource for troubleshooting, maintenance, and method refinement. Perform compliance and documentation: ensure all activities comply with lab quality management systems and regulatory requirements; maintain detailed records of instrument conditions, calibration, maintenance, and method development activities; support audits by providing documentation and demonstrating compliance with SOPs and procurement agreements. Assists the Laboratory Manager in the administration of the laboratory by making recommendations concerning instrumentation and equipment purchases. Minimum Qualifications: A bachelor's degree from an accredited college or university in chemistry, biology, limnology, botany, zoology, environmental science, or a field directly related to analytical chemistry and five years professional experience in laboratory analysis. Comparable professional experience can substitute on a year-for-year basis for the required college education. A chemistry degree and experience with Inductively Coupled Plasma (ICP) instruments is preferred. SJRWMD has determined this to be a mandatory-testing position as described in Section 440.102, Florida Statutes. Any offer of employment for a mandatory-testing position will be contingent upon successfully passing a drug screening paid for by SJRWMD. The SJRWMD Drug Free Workplace Policy is available for review in the Careers section at *************** Working Conditions: Work in lab wearing lab coat, gloves and eye protection as required by Chemical Hygiene Plan and Standard Operating Procedures; may stand for prolonged periods of time, performs tasks with equipment set-up in a fume hood; lift and carry heavy packages and coolers, safely manage toxic and hazardous chemicals. Additional Details: Starting Salary Range: $61,318.40 - $76,648.00 Starting salary is based on qualifications and experience. Benefits include Florida Retirement System, paid parental leave, health insurance, dental insurance, life insurance, long-term disability, paid leave and holidays, professional development, wellness program and eligible for public service student loan forgiveness program. Your application will receive careful consideration and, if selected for an interview, you will be contacted to schedule an appointment. St. Johns River Water Management District participates in E-Verify. E-Verify is an internet-based system that allows businesses to determine the eligibility of their employees to work in the Unites States. Certain service members and veterans, and the spouses and family members of such service members and veterans will receive preference in employment and are encouraged to apply. Equal Employment Opportunity/Veterans' Preference/Drug-Free and Tobacco-Free Workplace Location: Palatka Closing Date: Open until filled

Join Our Team at Florida Credit Union - Where Your Future Shines Bright! About Us: At Florida Credit Union, our mission is clear: to enhance the lives of our Florida neighbors through exceptional financial services. When you become a part of our team, you're not just starting a new job; you're joining a vibrant community dedicated to making a positive impact. We pride ourselves on fostering a dynamic, collaborative work environment where every team member is valued and supported. Why You'll Love Working with Us: Dynamic Team Environment: Work in a supportive and collaborative atmosphere where your ideas and contributions are valued. Extensive Training: Receive comprehensive training to ensure you're set up for success from day one. Exceptional Benefits: Enjoy a competitive benefits package designed with your well-being in mind. Career Growth: Explore numerous opportunities for professional development and advancement within our organization. Position Overview: Assist the SVP and VP of Consumer Lending in all aspects of lending throughout all parts of the organization in accordance with policies, goals, and established objectives. Ensure that all loan policies and underwriting guidelines are followed and consistent quality loan decisions are made on loan requests not exceeding assigned loan limits. Your Key Responsibilities: Develop and deliver loan and sales related training to improve loan officer/MSR's underwriting skills. Meet regularly with branches to ensure quality underwriting. Assists in the management of all loan promotions in cooperation with operations and marketing. This includes the collection of data needed to track all results. Assuring all lending processes are efficient, both from a member service and sales perspective. Serve as an escalation point for issues and inquires relating to loan decisions and problem resolutions. What We're Looking For: Associate's degree in Marketing, Finance, or Business combined with 1-3 years of related experience, or an equivalent mix of education and hands-on experience. A current driver's license. Ready to Make a Difference? If you're passionate about supporting your community and eager to grow your career with a team that truly cares, we want to hear from you! Apply today and take the first step towards a rewarding career with Florida Credit Union. Become a vital part of our mission to support and uplift our members - apply now!

We are seeking a passionate, dedicated Quality Control Technician to ensure our products exceed industry standards and client expectations. With a focus on quality, sustainability, and innovation, we serve a diverse range of clients across commercial, residential, and infrastructure projects. As a Quality Control Technician, you will play a crucial role in maintaining the quality and integrity of our concrete products. You will be responsible for conducting tests, analyzing data, and developing solutions to improve product quality. This position requires a keen eye for detail, a strong understanding of concrete technology, and the ability to work collaboratively with intersecting departments at SRM such as operations, production, sales, and technical services. Key Responsibilities: Conduct routine and non-routine analyses of raw materials, in-process, and finished concrete products using industry-standard methods. Interpret test results, compare them to established specifications and control limits, and make recommendations on the appropriateness of data for release. Perform visual inspections of finished products to ensure compliance with quality standards and specifications. Collaborate with production teams to identify and troubleshoot production challenges that affect quality. Assist in the development and implementation of quality control training programs for production staff. Maintain accurate and organized records of tests, analyses, and other quality-related activities. Stay updated with the latest trends, technologies, and regulations in the concrete industry to recommend improvements to our quality control processes. Qualifications Able to meet schedule requirements. Shifts vary based on scheduled pours. Candidates must be able to accommodate day shifts, as well as overnight shifts. ACI certification preferred Associate or bachelor's degree in Civil Engineering, Materials Science, Concrete Management, Construction Management, or related field is preferred. 1-3 years of experience in quality control or quality assurance, preferably in the concrete or construction materials industry. Strong understanding of concrete technology and testing methods. Excellent analytical skills and attention to detail. Effective communication and interpersonal skills. Ability to work independently and in a team environment. Proficiency in Microsoft Office and experience with quality management software. Willingness to undergo SRM's pre-employment screenings. About us: SRM strives to be the largest, most profitable construction material company in the country, while maintaining a best-in-class culture. SRM's 5 Principles of Service: Safety, Quality, Kindness, Cleanliness, Go-Getter Why Join Us? Our commitment to our team includes: Growth: Opportunities for advancement in a rapidly growing company. Home Daily: Enjoy work-life balance with daily home time. Competitive Compensation: Hourly pay with eligibility for bonuses and annual raises. Exceptional Benefits: Comprehensive benefits package including low-cost medical, dental, vision, STD, LTD, and life insurance, paid holidays, PTO and vacation programs, 401k with $100 match/week, family days, and more! Overtime Opportunities: Daily overtime after 8 hours and weekly after 40 hours Candidates will be required to undergo a pre-employment drug screen, SRM's pre-employment physical, and consent to background checks, including Clearinghouse and MVR checks. We are an equal-opportunity employer and value diversity at our company. We do not discriminate based on race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

About Us: H&A Farms is a family-owned, multigenerational agricultural business with operations in Orange, Lake, and Levy counties. The companies farming and packing operations manages 1,000+ acres and packs fruit for another 60+ growers throughout Florida and Georgia representing another 1,800+ acres. The company also has an agritourism business that operates as Amber Brooke Farms located in Eustis, Florida and provides u-pick, special events, festivals, and private event activities for nearly 10,000 guests every year. Job Summary: We are seeking a motivated and experienced Quality Control Specialist. In this role, you will be responsible for ensuring that the fruit we pack meets specific quality standards for freshness, appearance, and safety before they reach customers. This position is based in a fruit packing facility where temperatures typically range from 35°F to 55°F. Employees must be able to work comfortably and safely in a cool environment for extended periods of time while performing their job duties. The ideal candidate for this position should be well-organized and possess good communication skills. They should be comfortable with managing paperwork and utilizing information systems. A good understanding of quality control procedures is also important. Key Responsibilities: Inspect and test materials, equipment, processes, and products to ensure quality standards are met. Conducting tests and analyzing results to identify defects or inconsistencies in products and processes. Making recommendations for improvements based on the data collected during inspections. Collaborating with production and quality assurance teams to ensure compliance with quality standards. Maintaining accurate documentation of quality control tests and inspections. Qualifications: Work experience as a Quality Control Specialist or similar role in the fruit farm industry. Knowledge of food safety practices and prior experience working in environments where adherence to food handling standards is essential. Experience with relevant software, such as MS Office and data analysis software. Data collection and analysis skills. Computer knowledge and bilingual in Spanish and English is required. Join our team as a Quality Control Specialist and play a vital role in ensuring the excellence of our fruit while fostering a culture of continuous improvement within our organization. Job Type: Full-time Seasonal Work Location: In person

Description The SR Associate, Quality Control Data will manage the following functions in the Quality Control Department. This includes LIMS, Sample Life Cycle Management and Quality Control test documentation life cycle management in compliance with procedures and regulatory requirements. The incumbent will be responsible as an approved USDA sampler and providing Quality Assurance and Production support as needed. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.Duties & Responsibilities Sample Life Cycle Management including responsible for daily sample submission receipt (including the maintenance of the logbook, LIMS, coolers, and freezers), preparation of retention samples and maintenance of retention samples and retention database. Regulatory Compliance including responsible for preparation and shipment of USDA samples using APHIS Form 2020. Documentation Life Cycle Management including responsible for managing Quality Control test documentation of active ingredient and final product (filing and generating associated test reports). Data Integrity including responsible for Quality Control test record issuance and reconciliation. Information Support including functioning as a Quality Control liaison with Planning, Quality Assurance and Production to provide necessary information regarding samples and test dates to allow proper management of formulation and packaging activities and management of safety stocks and back-order prevention. Product Release including assisting in the preparation of accurate and timely submissions to USDA for product release using the APHIS Form 2008 and international documentation as needed to release product according to applicable procedures. As assigned, assists in Conditional Releases, Early Expiration, Spanish/Brazil/ROW assignments and document creation/revision as needed according to applicable procedures. Accountable to all related USDA, international, and GMP Biologics requirements at the Athens site for maintaining product registrations in >90 countries. Ensures quality samples and data in Quality Control through: Management of samples, Distribution, and reconciliation of test documentation, Filing of test documentation, Generation of test reports as well as Planning and Production support for testing information. Requirements Associates degree + 2 years of relevant industry experience required; Bachelor's degree in a scientific discipline, preferred. Functional knowledge of computer systems such as laboratory information management systems (LIMS) is required. Functional knowledge of product manufacturing activities is recommended. Previous experience in a Manufacturing environment in Quality Assurance, Quality Control, or Production preferred. Solid verbal and written communication skills, including document review and editing skills. Detail oriented. Strong time management skills. Strong organizational skills with ability to multi-task and prioritize. Experience in root cause analysis tools. Ability to understand and comply with Quality Assurance and regulatory requirements (9CFR, Outlines of Production, Change Control, Deviation, CAPA, OOX, etc.). Computer skills in Microsoft Office applications and the ability to learn new applications quickly and easily. Desired Skills, Experience and Abilities

Pay: $20. 00 - $29. 00 per hour Job description: Job Title: Quality Control Inspector - Electronics Assembly Company: Liberty Sta ing USA Location: Apopka, FL Pay: Based on experience Schedule: Monday-Thursday, 6:30 AM - 5:15 PM (10-hour shifts); Friday overtime as needed Job Type: Full-Time | Temp-to-Hire Overview Liberty Sta ing USA is seeking a detail-oriented Quality Control Inspector for electronics assembly in Apopka, FL. The ideal candidate is IPC-A-610 certi?ed and experienced in inspecting PCBs, cable assemblies, and box builds. This role ensures that all assemblies meet customer speci?cations and industry quality standards. Key Responsibilities ? Inspect electronic assemblies thoroughly per customer speci?cations and IPC standards. ? Perform ?nal inspections on PCB, box build, and cable assemblies prior to shipping. ? Read and interpret customer drawings, BOMs, and assembly instructions. ? Conduct First Article Inspections (FAI) at all stages of production. ? Verify SMT machine setups and perform solder paste audits before production. ? Conduct daily in-process audits across all departments. ? Use a microscope for precision electronic part and solder inspection. ? Hand solder to support rework or inspection when needed. ? Complete and maintain inspection and shipping documentation for outgoing assemblies. Quali?cations / Skills ? Minimum 1 year of experience in quality control / inspection of electronic assemblies. ? High School Diploma or equivalent. ? IPC-A-610 Certi?cation required. ? Pro?cient in microscope use for precision inspection. ? Knowledge of hand soldering techniques is a plus. ? Strong attention to detail and commitment to quality standards. Why Work With Liberty Sta ing USA? ? Competitive pay based on experience. ? Full-time, long-term, temp-to-hire opportunity. ? 4-day workweek with overtime opportunities on Fridays. ? Supportive team environment and opportunity to grow in the electronics manufacturing ?eld. Keywords for Visibility: Quality Control Inspector, Electronics Inspector, IPC-A-610, PCB Inspection, Cable Assembly, Box Build, SMT Inspection, Hand Soldering, Electronics Assembly, Apopka Jobs, Liberty Sta ing USA Careers, In-Process Audit, Final Inspection Apply today to join Liberty Sta ing USA as a Quality Control Inspector and advance your career in electronics assembly in Apopka, FL! Job Type: Full-time Bene?ts: ? Dental insurance ? Health insurance ? Vision insurance

**We are a precision CNC manufacturer seeking an experienced Quality Control (QC) Inspector. The QC Inspector is responsible for inspecting incoming materials, conducting in-process inspections, and ensuring that machined parts meet both the specifications of the drawings and the customer's quality standards.** Schedule & Pay **Pay: $22-$26/hr** **2nd Shift: M-TH 4:15pm - 2:45am (OT Friday 2PM-10:30PM)** Responsibilities + Conduct inspections of incoming materials. + Perform in-process inspections of products. + Ensure machined parts meet tight tolerance and customer quality standards. + Utilize measuring equipment such as micrometers, calipers, and gauges. + Conduct first article inspections. + Read and interpret blueprints and schematics. Essential Skills + Extensive experience with measuring equipment: micrometers, calipers, and gauges. + Familiarity with Geometric Dimensioning and Tolerancing (GD&T). + Experience with first article inspections. + Ability to read blueprints and schematics. + Basic computer and documentation skills. + Basic math skills. Additional Skills & Qualifications + High school diploma. + Experience with PCDMIS software (CMMS system). + Experience inspecting metals/tools in a shop setting. Why Work Here? **Join a company where precision and quality are valued, and where you can work in a supportive environment with a team of experts. Enjoy a structured work schedule that allows for work-life balance.** Work Environment **Work in a climate-controlled plant during the first shift from Monday through Thursday.** Job Type & Location **This is a Contract to Hire position based out of Apopka, Florida** **Job Type & Location** This is a Contract to Hire position based out of Apopka, FL. **Pay and Benefits** The pay range for this position is $22.00 - $26.00/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 Apopka,FL. **Application Deadline** This position is anticipated to close on Jan 31, 2026. **About Aerotek:** We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

The County Materials Family of Companies manufactures and delivers concrete construction products to meet the demand for growing communities. We rely on our talented and dedicated team members to provide reliable products with personalized service. We are seeking a Quality Control Technician for County Materials in Astatula, Florida Job Duties: * Performs quality control inspections, checks, and tests during the manufacture of products * Inspects materials, parts and products at different stages of production * Records observations and may make recommendations for improving processes * Familiar with standard concepts, practices, and procedures within the concrete industry * Regularly observes the production process including setup, casting, stripping and storage of product. * Work with production to identify and resolve quality issues related to casting and concrete performance. * Manage housekeeping to ensure a safe workplace. * Other tasks as needed Work Environment: * Work in indoor and outdoor weather conditions, including extreme hot or cold temperatures * Work near moving machinery and equipment - could include electrical hazards * Work in a noisy environment Physical Requirements: * Carrying/Lifting 10 - 40 Pounds frequently * Carrying/Lifting > 40 Pounds occasionally * Standing / Walking / Climbing * Squatting/Crouching/Kneeling/Bending * Pushing / Pulling / Reaching Above Shoulder Experience & Qualifications: * Understanding of a manufacturing environment. * Concrete plant and/or quality control experience highly desired. * Ability to interpret shop drawings and job specifications. * Proficient Computer Skills with Microsoft Office. * Solid math aptitude. * Must have the ability to train and obtain technical certifications as directed and supported by the company. * Ability to work independently. * Strong organizational, interpersonal and communication skills. * High School diploma or equivalency required. * 1-2 years prior experience in a manufacturing environment * Experience in the construction and/or building materials industry preferred, not required.

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Quality Systems Associate Summary: Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol. Primary responsibilities for role (level-specific responsibilities should be included in the chart below): * Completes weekly review of equipment QC and maintenance records. * Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they related to product quality and/or donor safety. * Inspects and releases incoming supplies. Investigates and reports supplies have not met quality specifications and requirements prior to use. * Performs documentation review for unsuitable test results. * Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include: * Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol. * Performs all product release activities. * Reviews lookback information and documentation. * Reviews waste shipment documentation. * Reviews unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process. * Reviews electronic donor chart exceptions impacting donor eligibility/safety and/or product quality. * Reviews donor deferral notifications from competitor centers. * Reviews plasma processing documentation to ensure the proper freezing, storage and handling of product. Quality Systems Associate * Assist the Quality Systems Manager to ensure center training programs follow procedural requirements as defined in the donor center SOP and/or training programs documents. Duties include: * Creates, maintains, and audits training records and files to ensure compliance. * Performs employee training observations to ensure staff competency prior to releasing employees to work independently. * Conducts required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations. * On an occasional basis, when the Quality Systems Manager is absent, the Quality Systems Associate may be required to perform the following duties: * Reviews and approves of deferred donor reinstatement activities. * Assists with completion of the internal donor center audit. Summary: * Performs review of monthly trending report. * Performs review of donor adverse events reports and the applicable related documentation. * Conducts training to address donor center corrective and preventative measures. This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed. Additional Responsibilities: Is certified and maintains certification as a Donor Center Technician. Knowledge, Skills, and Abilities: Developing command of interpersonal communication, organizational and problem-solving skills. Ability to understand FDA regulations. Strong integrity and commitment to quality and compliance. Good knowledge of mathematics. Legible handwriting. Proficiency with computers. Ability to work flexible scheduling to meet business needs. Performs basic document review and employee observations. Communicates openly with the CQM on issues noted during reviews. Ability to understand and follow SOP's and protocols. Ability to perform primary responsibilities of the Quality Associate role in a proficient manner. Has a basic understanding of cGMP and quality systems. Is able to spend hours sitting and reviewing documentation for accuracy. Demonstrates good organizational skills and attention to detail. Education: High school diploma or GED. Obtains state licensures or certifications if applicable. Experience: Typically requires no previous related experience. Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups. #biomatusa Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws. Location: NORTH AMERICA : USA : FL-Gainesville:BTGNS - Gainesville FL-NW 13th St-BPC

Full-time Description JE Technology Solutions, Inc., a designer and manufacturer of Aircraft Ground Equipment, is seeking a talented, experienced, and highly-analytical Quality Control Inspector to join our production department. As a Quality Control Inspector, you will uphold the safety regulations of our company and supervise the production process to guarantee that all our products meet quality expectations. The chosen candidate will perform regular product evaluations, record inspection results, and recommend improvements to the production process. To excel in this role, applicants should demonstrate great attention to detail with excellent technical and math abilities. Responsibilities: · Perform regular quality assessments on all incoming materials from vendors and outgoing products for shipping. · Reject all products and materials that fail to meet quality expectations. · Read drawings and specifications to understand the requirements of products and services. · Utilize tools such as eDrawings and Isometric Views on drawings to verify orientation of items during inspection. · Measure product dimensions, examine functionality and compare the final product to the specifications. · Recommend improvements to the production process to ensure quality control. · Document inspection outcomes by completing detailed reports. · Measure and record Quality Control related KPIs, such as First Pass Yield. · Communicate and confirm defects have been corrected with the production team. · Promote Quality-At-The-Source best practices to improve product excellence. · Ability to problem solve using tools like “ask five whys”. · Observe the production process. · Prioritize prompt response to production floor to ensure continuous flow of production. · Collaborate with the quality and manufacturing teams to resolve quality-related issues in a timely manner. · Participate in functional testing of products such as load testing, electrical testing, pressure testing, etc. · Ability to follow company Standard Operating Procedures and uphold Workmanship Standards. · Add occasional need to travel for field inspections including military bases. Requirements High school diploma or equivalent qualification. Certification in quality control is preferred. A minimum of 2 years' experience in a similar role. Excellent knowledge of MS Office. Good math and technical skills. Strong understanding of quality control standards and testing techniques. Willing to work shift from 5:00 a.m. to 3:30p.m., 4 days/week. Preferred Skills: · Quality Inspection · Welding Inspection · Proficiency with inspection equipment, such as: o Tape Measure o Calipers o Dial Indicator o Multimeter o Pressure Gauges o Thread Gauges o Gauge Blocks · Familiarity with PCMM inspection equipment including probe and scanner attachments is a plus · Quality Control · Dimensional Inspection · ISO 9001:2015 Awareness · Experience with GD&T is a plus · Manufacturing Processes and Procedures · Familiarity with AS9100 is a plus · Experience with NDT and Magnetic Particle Inspection is a plus JE Technology Solutions, Inc. is a Drug Free Workplace. All offers of employment by JE Technology Solutions, Inc. are contingent on completion of a drug test within 2 business days of your offer acceptance and a background check with results in compliance with company policy. JE Technology Solutions, Inc. uses E-Verify to confirm employment eligibility for roles based in the United States. JE Technology Solutions is an Equal Opportunity Employer. All applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender identity, national origin, veteran or disability status.

Focuses on analytical laboratory activities for specific testing involving HPLC; in addition, participation in a variety of food quality control analytical/microbiological support activities is required. Work is performed through the application of a body of knowledge related to standard laboratory methods, practices, procedures, policies, regulations, and laboratory materials and equipment. Duties and Responsibilities: * Operates and maintains HPLC units * Prepping and running samples following established protocol, responsible for maintaining instruments, calibrating, and following maintenance regimen. * Prepare eluent and required reagents. Responsible for accuracy in the preparation of reagents, eluents, and standards. * Performs chemical and physical analyses on a variety of samples, including food products and intermediate samples. * Tests include but are not limited to organoleptic evaluations, pH, acidity titrations, sodium, nitrate/nitrite analyses, Brix, moisture, specific gravity, moisture, pulp content, etc. * Performs required calculations and posts/maintains required spreadsheets. * Performs microbiological analyses on a variety of products, following required aseptic techniques in media prep, sample collection, plating and bacteria identification. * Logs samples and related pertinent information. Follows appropriate documentation and record-keeping procedures. * Performs related work as assigned. Skills & Qualifications * Proficient in chemistry and laboratory procedures. * Attention to detail and strong documentation skills. * Troubleshooting and root cause analysis. * Proficiency in quality assurance, microbiology, quality control, and GMP. * Bachelor's degree or Diploma in Food Science, Quality, or related discipline is preferred Job Type & Location This is a Contract to Hire position based out of Eustis, FL. Pay and Benefits The pay range for this position is $21.50 - $21.50/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 Eustis,FL. Application Deadline This position is anticipated to close on Feb 2, 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.

Disclaimer: Please note, if you are selected to have an interview with Thermacell, you will receive an email from our applicant tracking system Paylocity (**********************************) or an email from a Thermacell.net domain. Be aware of phishing emails/text messages. Thermacell will never text or Skype you about your candidacy or personal confidential information. If you are unsure, please contact **********************. THE COMPANY Thermacell Repellents, Inc. is on a mission to liberate people who love the outdoors from the harmful effects of insects. Thermacell makes the world's leading zone mosquito repellent, using our proprietary technology to create a zone of scientifically proven protection up to 20ft so people and pets can enjoy their time outdoors. Founded in 1999 and based outside of Boston in Bedford, Massachusetts, Thermacell has an ever-expanding product line and is trusted by over 6 million consumers worldwide to provide protection for outdoor events from backyard nights to rugged camping weekends. We aim to change the way people repel insects, through our award-winning products, disruptive innovation, and expanding distribution across multiple retail & e-comm channels in over 30 countries across the globe. Thermacell is a wholly owned subsidiary of a privately held global consumer products company and operated independently. Thermacell is home to 125+ full-time employees across three U.S. hubs - Bedford, MA (Corporate Headquarters), Buford, GA (Manufacturing & Distribution), and Hampton, FL (Science & Research Center) - and is expanding its footprint in the UK & Europe. ROLE PURPOSE: Thermacell is seeking a Chemistry Technician to support formula development, and analytical and quality testing. This position will report directly to the Science Manager, and serve as a part of the Science and Research Team in Hampton, FL. STATUS: Non-Exempt WORKING HOURS: Typically, between 8-5pm M-F (open to some flexibility) WORK LOCATION: Science and Research Center 6393 Navarre Ave, Hampton, FL 32044 Please note: This position is not eligible for work authorization sponsorship by the company now or in the future. Candidate must be authorized to work for any employer in the United States on a full time basis. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES: In this role, you'll get to: Independently execute accurate and timely quality testing in support of the manufacturing team and raising potential issues in an expedient manner Follow established SOPs to support technical aspects of Thermacell's chemistry program Conduct Good Laboratory Practice (GLP) and non-GLP laboratory studies assessing product performance, quality, safety, and chemical composition Maintain an orderly and safe laboratory and workspace Track, organize, and replenish laboratory supplies by conducting routine inventory assessments and working with vendors to fulfill purchasing needs Perform routine maintenance and troubleshooting of equipment Assist in the development of new formulas that meet performance targets Assist in other duties as assigned to support Science Department and global business activities THE IDEAL CANDIDATE: Lives our core values of Drive, Ownership, Integrity, Teamwork and Evolution Authentic and personable, humble, smart Relentless work ethic juiced by results, not titles or activities Externally competitive, internally collaborative Highly resourceful. Hands-on and practical Chooses curiosity and a commitment to learning over being right Radically candid - always with positive intention Motivated by challenge, resilient in the face of setbacks or adversity Able to critically think and navigate within a variety of ambiguous situations Even keeled energy, brings calm to chaos, low drama Make impeccable agreements, delivers end to end results with excellence Makes high quality data-based decisions with autonomy Unquenchable thirst for learning and self-improvement Effective communicator meeting people where they are Manages multiple, complex, and competing priorities Can anticipate data needs to support existing products and new product applications Maintains and delivers timely, accurate reports to support the global business Shows STRONG attention to detail and accuracy Is a highly resourceful problem solver that is not discouraged by creative troubleshooting Has proven ability to handle confidential information with discretion and maturity Believes safety is paramount COMPENSATION Compensation for this position will include a competitive base salary and an Annual Target Bonus opportunity. Details provided separately. We are proud to offer a competitive & valuable benefits package that enables you to protect your health, your family, and your way of life. It includes best-in-class medical & dental insurance where Thermacell pays for 82.5% of the premiums. Thermacell pays for the first half of your medical deductible through our Health Reimbursement Account for PPO & HMO Plans as well as contributes to your Health Savings Account if you enroll in the HSA plan. Long & Short-term Disability & Group Term Life insurance is also available at no cost to you. Paid time off for this position will consist of accrued vacation at a competitive level, along with 11 Holidays and a day off for your Birthday! 40 hours of wellness time is also available on your first day of employment. Additionally, a company shutdown period is offered for one week between Christmas and New Year's Day where the majority of business operations pause, and employees are encouraged to rest and recover together. Critical functions may require limited coverage to ensure business continuity. Additionally, you will have access to a variety of additional benefits such as vision, supplemental life, critical illness, Medical Flexible Spending Account, Dependent Care Flexible Spending Account, accident, SecureSave savings account, Employee Assistance Program, product benefit, wellness benefit, financial coaching and pet insurance for your furry family members! You can find all these details and more in our benefits guide along with additional discounts. You will be eligible for the employer 401K match up to 4% after completing one year of service. WHY WORK HERE? We are proud of our company culture - it's the fuel behind our dynamic and buzzing community! Our people are authentic, competitive, and compassionate. It's truly a unique formula for success. We believe in the virtuous cycle of thriving employees fueling a thriving business. We believe in growing great leaders and helping people to unleash their full human potential. We believe in creating a frictionless organization where clarity and empowerment to do the work that matters as fast as possible. We believe in making impeccable agreements and relentlessly tracking exceptional results and celebrating achievements together! We believe in creating inspiring impact everywhere we can in support of our mission where everyone can be a force multiplier. OUR CORE VALUES: Drive - An optimistic can-do spirit, a passion to delight our consumer, a belief in the importance of determination and the freedom to make a difference. Ownership - We are empowered to take accountability for our contributions and desire to do the highest quality work with responsible urgency to drive business results. Integrity - We will always do the right thing guided by truth and sincerity. We exercise constructive candor and have the willingness to challenge and be challenged in all interactions. Teamwork - The belief that we is greater than me, and with collective brainpower we are better together. We are a community of compassionate support and collective success. We win as one and play hard in celebration together. Evolution - We are committed to continuous improvement, always learning, growing, and adapting to constant change. We seek progress over perfection. OUR COMMITMENT: Thermacell is committed to preserving a culture of diversity, inclusion, and belonging. The collective sum of our individual differences, knowledge, life experiences, and unique talents represents a significant part of our culture and is the foundation for our accomplishments and impact. We strive to create a supportive community where we all can show up as our authentic selves and are confident and comfortable to be genuine with our teammates in our day-to-day work environment. We are proud to be an equal-opportunity employer. We do not discriminate on the basis of race, color, religion, citizenship, national origin, sex (including pregnancy), sexual orientation, gender identity or expression, age, physical or mental disability, veteran status, marital status, genetic information, or any other characteristic protected by state, federal or local law. OUR AWARDS: Great Place to Work Award 2025 | New York Times Wirecutter pick for “The Best Mosquito Control Gear for your Patio or Yard” 2021-2025 | CNN Underscored Editor's Pick 2024-2025 | Men's Journal Outdoor Award 2025 | Shop TODAY Expert Pick 2025 | Canadian Grand Prix New Product Award 2024 | Outside Gear Guide Editor's Choice 2022 | Time Magazine Best Inventions 2022 | This Old House Editor's Choice | Good Housekeeping Home Products Award | CES New Tech Award - IDEA Good Design Award | Canadian Tire Digital Excellence Award | LIV Smart Mosquito Repellent System - CES TWICE Awards 2021-2022 | Good Housekeeping Research Institute #1 Tabletop Mosquito Repellent | Field & Stream “Best of the Best” Award | Backpacker Magazine - Best Backpacking Accessory 2019 | New York Times Wirecutter - Best Car Camping Gear 2018 | Popular Mechanics - Grand Award Winner - Recreation - Best of What's New 2018 Requirements SKILLS/KNOWLEDGE/EXPERIENCE REQUIRED Bachelor's degree in chemistry or related field Formulation and/or analytical chemistry experience; professional experience and/or experience with pesticide or bioactive products preferred Experience following laboratory procedures and protocols; GLP experience preferred Direct expertise in the use of a range of analytical chemistry instrumentation, specifically GCMS, GC-FID, UPLC and/or HPLC Familiarity with quality control concepts Proven ability to plan, organize, problem solve, and coordinate multiple tasks Proven ability to document accurate data in official laboratory records and summarize findings in technical reports Ability to stand for extended periods of time (4 or more hours) and conduct repetitive laboratory tasks Ability to perform basic math calculations Proficiency with wet chemistry techniques, e.g. using pipets and preparing solutions Proficiency with Microsoft Office 365 and related software Salary Description $49,900 - $66,000

What We Do FOX Factory designs, engineers, manufactures and markets performance-defining products and systems for customers worldwide. Our premium brand, performance-defining products and systems are used primarily on bicycles, side-by-side vehicles, on-road vehicles with and without off-road capabilities, off-road vehicles and trucks, all-terrain vehicles, snowmobiles, specialty vehicles and applications, motorcycles, and commercial trucks. Some of our products are specifically designed for and marketed to a variety of leading cycling and powered vehicle original equipment manufacturers ("OEMs"), while others are distributed to consumers through a global dealer and distribution network. Fox Factory Holding Corp. is the holding company of FOX Factory, Inc. and is publicly traded (FOXF) on Nasdaq. Why you should join us Not only do we provide competitive wages, you will also have access to great benefits and employee discounts. But more importantly, it's a fun environment where we truly enjoy working as a team and bringing great products to our customers! If this sounds like something you would love to do, and a place you want to be a part of, get in touch with us by submitting your application. We look forward to hearing from you! Position Summary: Inspects finished products, products being processed, incoming materials, parts and assemblies, etc. for conformance to company standards. Position Responsibilities: Checks randomly selected samples and verifies accuracy of equipment or process. Reports conditions requiring immediate repair. Uses advanced inspection methods to develop and conduct quality programs. Works under general supervision. Keeps records and makes reports indicating results of inspections. Uses experience and judgment for planning and accomplishing goals. May inspect work areas to detect unsafe conditions. May obtain samples to conduct studies in laboratory analysis and determines measures to be taken to remedy deviations from standards. Conduct Product and Process audits and LPA (Layered process audits). Specific Knowledge, Skills or Abilities Required: Strong and accurate data entry skills Intermediate skills in using Microsoft tools (Outlook, Word, Excel) Excellent organization skills Excellent problem-solving skills. Self-motivated - able to work with minimal supervision Use of powered hand tools Operating a Forklift Testing of raw materials and/or finished products, which may or may not include industry standard test methods (e.g. ANSI/ASME measuring standards) Position Qualifications: Education: HS graduate or equivalent Experience: 1+ years of experience in quality and/or inventory Previous experience with Geometric Dimensioning and Tolerancing (GD&T) Previous experience with Oracle, SAP or other database management systems Shift: Mon-Fri, 7am-3:30pm Work Environment and Physical Requirements: Activity Constantly - 6+ hours : Stand, Walk, Twist/Turn, Stoop/Bend Frequently - 3 to 6 hrs. : Lift to 50 lbs. Manufacturing Environment Working in hot and cold climates Personal Protective Equipment - Ear protection is readily available in high level noise areas Working around machinery with moving parts Working around moving objects or vehicles, Potential for slippery and uneven walking surfaces including use of ladders Working in close proximity to others Exposure to offensive odors Vision abilities required to validate and enter data on computer as well as calibrated measurement tools Exposures to and working with hazardous waste Disclaimer : This list does not represent all physical demands. Descriptions are representative of those that must be met by employee to successfully perform the essential functions of the job. Reasonable accommodation may be provided to enable individuals with disabilities to perform the jobs' essential functions. Note: FOX provides equal employment opportunities for all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, gender identity, sexual orientation, marital status, religion, age, physical disability (including HIV and AIDS), mental disability, results of genetic testing, or service in the military, or any other characteristic protected by the laws or regulations of any jurisdiction in which we operate. We base all employment decisions -including recruitment, selection, training, compensation, benefits, discipline, promotions, transfers, layoffs, terminations and social/recreational programs - on merit and the principles of equal employment opportunity. Fox offers an excellent compensation package and wide-ranging opportunities for professional development. Medical, Dental, Vision, Health Spending and Dependent Care Savings Accounts, Disability and Life Insurance benefit programs are available, as is a 401k plan with employer matching. Eligibility for all benefit programs is defined by the applicable plan document or employee handbook.

Job DescriptionBenefits: 401(k) matching Competitive salary Dental insurance Health insurance Paid time off Vision insurance Structural Steel Certified Welding Inspector (CWI)/QC) Structural steel fabricator in Leesburg, Florida is seeking an experienced Certified Welding Inspector (CWI). We are looking for a team player with experience in AISC standards and audits. This is a non-traveling position, which reports to the QC Manager. EDUCATION EXPERIENCE: High school diploma or equivalency certificate. 3+ years of experience as a certified welding inspector in a structural steel fabrication facility, as well as experience in Quality Assurance. Current American Welding Society certified welding inspector (CWI). Ability to read and understand drawings plans and specifications. Ability to perform physical activities that require frequent bending at the waist, squatting, climbing, kneeling and reaching about the head. Must be detail-oriented, extremely organized and have a good work ethic. Microsoft Office skills, including Excel, required. Experience working in fabrication shop UT and MT certification is required AISC standards/audit experience highly preferred. RESPONSIBILITIES: Maintain Quality Control Manual, including compliance to all AISC standards. Position involves visual inspection of structural steel, including bolted and welded connections, and performing non-destructive testing. Interpret codes and specifications in accordance with the drawing requirements. Use a computer to compile and submit data of acceptance or rejection of inspections, as well as for inter-office communications and audit program management. Recommend and approve repairs as well as perform visual inspection of work in progress and completed work. Review and verify welding procedures and welder qualifications. Review Mill test reports and certifications

Job DescriptionDescription: JE Technology Solutions, Inc., a designer and manufacturer of Aircraft Ground Equipment, is seeking a talented, experienced, and highly-analytical Quality Control Inspector to join our production department. As a Quality Control Inspector, you will uphold the safety regulations of our company and supervise the production process to guarantee that all our products meet quality expectations. The chosen candidate will perform regular product evaluations, record inspection results, and recommend improvements to the production process. To excel in this role, applicants should demonstrate great attention to detail with excellent technical and math abilities. Responsibilities: · Perform regular quality assessments on all incoming materials from vendors and outgoing products for shipping. · Reject all products and materials that fail to meet quality expectations. · Read drawings and specifications to understand the requirements of products and services. · Utilize tools such as eDrawings and Isometric Views on drawings to verify orientation of items during inspection. · Measure product dimensions, examine functionality and compare the final product to the specifications. · Recommend improvements to the production process to ensure quality control. · Document inspection outcomes by completing detailed reports. · Measure and record Quality Control related KPIs, such as First Pass Yield. · Communicate and confirm defects have been corrected with the production team. · Promote Quality-At-The-Source best practices to improve product excellence. · Ability to problem solve using tools like “ask five whys”. · Observe the production process. · Prioritize prompt response to production floor to ensure continuous flow of production. · Collaborate with the quality and manufacturing teams to resolve quality-related issues in a timely manner. · Participate in functional testing of products such as load testing, electrical testing, pressure testing, etc. · Ability to follow company Standard Operating Procedures and uphold Workmanship Standards. · Add occasional need to travel for field inspections including military bases. Requirements: High school diploma or equivalent qualification. Certification in quality control is preferred. A minimum of 2 years' experience in a similar role. Excellent knowledge of MS Office. Good math and technical skills. Strong understanding of quality control standards and testing techniques. Willing to work shift from 5:00 a.m. to 3:30p.m., 4 days/week. Preferred Skills: · Quality Inspection · Welding Inspection · Proficiency with inspection equipment, such as: o Tape Measure o Calipers o Dial Indicator o Multimeter o Pressure Gauges o Thread Gauges o Gauge Blocks · Familiarity with PCMM inspection equipment including probe and scanner attachments is a plus · Quality Control · Dimensional Inspection · ISO 9001:2015 Awareness · Experience with GD&T is a plus · Manufacturing Processes and Procedures · Familiarity with AS9100 is a plus · Experience with NDT and Magnetic Particle Inspection is a plus JE Technology Solutions, Inc. is a Drug Free Workplace. All offers of employment by JE Technology Solutions, Inc. are contingent on completion of a drug test within 2 business days of your offer acceptance and a background check with results in compliance with company policy. JE Technology Solutions, Inc. uses E-Verify to confirm employment eligibility for roles based in the United States. JE Technology Solutions is an Equal Opportunity Employer. All applicants will receive consideration for employment without regard to race, color, religion, sexual orientation, gender identity, national origin, veteran or disability status.

Job Summary: Focuses on analytical laboratory activities for specific testing involving HPLC; in addition, participation in a variety of food quality control analytical/microbiological support activities is required. Work is performed through the application of a body of knowledge related to standard laboratory methods, practices, procedures, policies, regulations, and laboratory materials and equipment. Duties and Responsibilities: Operates and maintains HPLC units Prepping and running samples following established protocol, responsible for maintaining instruments, calibrating, and following maintenance regimen. Prepare eluent and required reagents. Responsible for accuracy in the preparation of reagents, eluents, and standards. Performs chemical and physical analyses on a variety of samples, including food products and intermediate samples. Tests include but are not limited to organoleptic evaluations, pH, acidity titrations, sodium, nitrate/nitrite analyses, Brix, moisture, specific gravity, moisture, pulp content, etc. Performs required calculations and posts/maintains required spreadsheets. Performs microbiological analyses on a variety of products, following required aseptic techniques in media prep, sample collection, plating and bacteria identification. Logs samples and related pertinent information. Follows appropriate documentation and record-keeping procedures. Performs related work as assigned. Skills laboratory, Quality control, Gmp, Chemistry, Hplc, Quality assurance, Wet chemistry, Analysis Top Skills Details laboratory,Quality control,Gmp Additional Skills & Qualifications Manual skills: Ability to lift to 40 lbs. Manual labor required for this position. Occasional exposure to odors, dusts/powders and noise. Wearing of hairnet, facial hair covering (if applicable), hearing protection, mask, lab coat and goggles are required. Knowledge of laboratory tests and analyses. Strong attention to detail. Multitasking capability Self-motivated Must be able to stand for extended periods of time Comply with company regulations on personal protective equipment Ability to handle samples and laboratory equipment. Ability to handle heavy weight (up to 40 lbs.) Ability to make mathematical computations. Ability to keep records. Ability to communicate effectively. Ability to work in a team environment. Ability to organize and carry out assigned task or program. Ability to adapt new technology and methods to enhance program effectiveness. Experience Level Intermediate Level Job Type & Location This is a Contract to Hire position based out of Eustis, FL. Pay and Benefits The pay range for this position is $21.50 - $21.50/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 Eustis,FL. Application Deadline This position is anticipated to close on Feb 2, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.