Quality control technician jobs in Gainesville, GA

Overview: Performs 3D Lab procedures at a technical level not requiring constant supervision of extremely technical detail. Performs technical procedures that require independent judgement, ingenuity and initiative to produce 3D modeling. Responsibilities: Performs 3D Lab procedures at a technical level not requiring constant supervision of extremely technical detail. Performs technical procedures that require independent judgement, ingenuity and initiative to produce 3D modeling. Qualifications: Education Graduate of an AMA approved Radiologic Technology program Required Work Experience 2 years A minimum of previous job-related experience in CT, MRI, IR, US or Nuclear Medicine Required Licenses and Certifications Registered by the American Registry of Radiologic Technology (R), Vascular Interventional Radiography (VI), Computer Assisted Tomography (CT) or Magnetic Resonance Imaging (MR) Required Additional Licenses and Certifications BLS certified Required Business Unit : Company Name: Piedmont Hospital

Company: Fusion Medical Staffing Job Details Fusion Medical Staffing is seeking a skilled Cath Lab Tech for a 13-week travel assignment in Cumming, Georgia. As a member of our team, you'll have the opportunity to make a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team. Required Qualifications: One year's recent experience as a Cardiac Cath Lab Tech Current BLS (AHA/ARC) certification ARRT, RCES, or RCIS certification Current ACLS (AHA/ARC) certification Preferred Qualifications: Valid Radiologic Technologist license in compliance within state regulations PALS (AHA/ARC) or ENPC Certifications Other certifications and licenses may be required for this position Summary: The Cath Lab Technologist is responsible for assisting in diagnostic and interventional cardiovascular procedures in the cardiac catheterization lab. This role involves preparing patients and equipment, monitoring hemodynamic data, assisting physicians during procedures, and ensuring patient safety throughout the process. The technologist operates specialized imaging equipment, maintains sterile technique, and collaborates with the healthcare team to provide high-quality patient care. This position requires technical expertise in cardiovascular procedures, critical thinking skills, and the ability to work efficiently in high-pressure situations. Essential Work Functions: Prepare and position patients for cardiac catheterization, angioplasty, stent placement, electrophysiology studies, and other interventional procedures Assist physicians during procedures by passing catheters, wires, balloons, and stents, and operating fluoroscopy and hemodynamic monitoring equipment Operate and maintain imaging equipment, contrast injectors, and hemodynamic monitoring systems, ensuring proper functionality Scrub in and assist with sterile field setup, ensuring adherence to infection control and procedural protocols Perform sheath removal and hemostasis using manual compression or closure devices as directed Maintain accurate documentation, including patient records, imaging data, and equipment logs Assist with inventory management, stocking supplies, and ensuring proper storage of sterile instruments and medications Adhere to radiation safety protocols, ensuring proper use of lead aprons, shields, and dosimeters Ensure compliance with hospital policies, safety guidelines, and regulatory requirements Adhere to hospital safety protocols, infection control guidelines, and regulatory standards Perform other duties as assigned within the scope of practice Required Essential Skills: Critical thinking, service excellence, and good interpersonal communication skills The ability to read, write, and communicate in the English language Ability to read/comprehend written instructions, follow verbal instructions, and proficiency in PC skills Physical Abilities - Must be able to remain in a stationary position, move about, move equipment (50-100lbs), push, pull, and bend Interpersonal Skills - Must be able to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and professionalism Technical/Motor Skills - Must have the ability to grasp, perform fine manipulation, push/pull, and move about when assisting with procedures and/or using department equipment Mental Requirements - Must be able to cope with frequent contact with the general public and customers while meeting deadlines under pressure. Must be able to work under close supervision occasionally, as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail Sensory - Must possess visual acuity and ability to effectively communicate Benefits Include: Highly competitive pay for travel professionals Comprehensive medical, dental, and vision insurance with first day coverage Paid Time Off (PTO) after 1560 hours Life and Short-term disability offered 401(k) matching Aggressive Refer-a-friend Bonus Program 24/7 recruiter support Reimbursement for licensure and CEUs Why Choose Fusion? At Fusion Medical Staffing, our goal is to improve the lives of everyone we touch, and we're always looking for people like you to join our mission. Your passion for helping others deserves a partner just as committed to supporting you - that's why we offer day one insurance, $0 copay for mental health services, scholarships and awards, exclusive discounts, and more. From your personal recruiter to our clinical and traveler experience teams, we're here to guide and celebrate you along your journey. You take care of others; we take care of you. Other Duties Disclaimer: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned. This job description is not a comprehensive list of all activities, duties, or responsibilities that are required of the employee for this job and is subject to change at any time with or without notice. Start your rewarding career as a Travel Cath Lab Tech with Fusion Medical Staffing and join our mission to improve lives. Apply now! *Fusion is an EOE/E-Verify Employer #pb10

Ponya Lab Services, a division of Ponya, focuses on delivering research and technical services to improve health systems and community outcomes. By leveraging science-driven insights, Ponya Lab Services provides practical solutions for organizations in the health sector. With a commitment to innovation and excellence, we aim to make a meaningful impact through evidence-based practices and collaborative efforts. Job Summary The Laboratory Technologist plays a critical role in conducting various laboratory tests on biological samples to aid in patient diagnosis and treatment. Responsibilities include operating and maintaining laboratory equipment, preparing samples for analysis, conducting quality control procedures, interpreting and reporting test results, and maintaining accurate records. With a focus on precision and efficiency, the Laboratory Technologist collaborates with healthcare professionals to deliver timely and reliable test results. Specialized knowledge in a specific area, such as toxicology, may be required for certain positions. Certification and experience in clinical laboratory science are typically necessary for this role. The Laboratory Technologist's contribution ensures the delivery of high-quality laboratory services that support patient care and medical research. Job Description: Perform various laboratory tests to analyze biological samples for the presence of toxic substances Operate and maintain laboratory equipment used in toxicology testing Prepare samples for analysis following established protocols and procedures Conduct quality control procedures to ensure the accuracy and precision of test results Interpret and report test results accurately and promptly Maintain detailed records of tests performed Follow safety protocols and procedures to ensure a safe working environment Collaborate with other healthcare professionals to provide accurate and timely test results for patient care Stay current with advances in toxicology testing methodologies and technologies Qualifications: Bachelor's degree in Medical Laboratory Science, Clinical Laboratory Science, or a related field Specialization or certification in toxicology is preferred Previous experience working in a clinical laboratory setting, especially in toxicology Strong knowledge of laboratory procedures, equipment, and safety protocols Certification as a Medical Laboratory Scientist (MLS) or equivalent certification in toxicology is preferred Excellent attention to detail and organizational skills Ability to work effectively both independently and as part of a team Strong communication skills for interacting with colleagues and healthcare professionals Ability to handle confidential information with discretion

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: Lead and motivate the performance of key quality teams in support of manufacturing. Drive improvements for quality control processes and procedures. Position Responsibilities: * Gives direction and improvement recommendations for quality processes. * Ensures compliance with quality control standards. * Monitors quality processes. * May conduct quality training programs for technicians, inspectors and/or for the production line. * Mentors quality and line staff and facilitates problem solving. * Maintains standard quality practices across all processes. * Records data, makes computations, analyzes results, and writes reports. Specific Knowledge, Skills or Abilities Required: * Ability to work with cross-functional teams * Strong leadership ability * Strong manufacturing knowledge (5S, Lean Manufacturing, technical drawing understanding) * Familiarity with MS Office, Excel, and Outlook Position Qualifications: Education: HS Graduate, AA degree in a technical discipline or equivalent experience Experience: 5+ years prior quality control experience required, preferably in manufacturing environment People leadership experience desired, but not required Work Environment and Physical Requirements: Production/Manufacturing environment Lifts up to 50 lbs. on a regular basis Requires walking, standing, bending and lifting for long periods of time Vision abilities required to validate and enter data on computer 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.

Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in Artificial Intelligence and Machine Learning (AI/ML) risk management. As a Tech Risk & Controls Lead in Cybersecurity and Technology Controls line of business, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of AI/ML technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities Ensure effective identification, quantification, communication, and management of AI/ML technology risk, focusing on root cause analysis and resolution recommendations Develop and maintain robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals Execute reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work Proactively monitor and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance Required qualifications, capabilities, and skills 5+ years of experience or equivalent expertise in technology risk management, information security, or related field, emphasizing risk identification, assessment, and mitigation Familiarity with AI/ML risk management frameworks, industry standards, and financial industry regulatory requirements Proficient knowledge and expertise in data security, GenAI/LLM & AI systems, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives Preferred qualifications, capabilities, and skills Experience with security and technology risk management approaches for GenAI/LLM and Agentic AI Systems. CISM, CRISC, CISSP, or similar industry-recognized risk and risk certifications are preferred

Who is Habasit? Habasit is the global leader in the manufacturing of lightweight conveyor belting. Our slogan “Solutions in Motion” defines us; we are a provider of world class power-transmission and conveying solutions. At Habasit, we understand that a global leader is only as good as the people who represent it, and we are always searching for the right people to keep us in motion. We are looking for ambitious individuals, leaders, and students who are ready to help move us forward. If you have a can-do attitude and want to join a world-class organization, read on and apply today! SUMMARY The Quality Technician is primarily responsible for managing and driving root cause and corrective actions within the manufacturing & business environment. This role ensures that product and process nonconformities are properly investigated, documented, and resolved in compliance with company procedures. The Quality Technician partners with cross-functional teams to identify root causes, implement effective solutions, and monitor results to prevent recurrence. This role is ideal for someone who thrives on problem-solving, compliance, and driving accountability across teams. Things you should know about Habasit's opportunities: Direct hire opportunity Eligible for bonuses and incentives $500 bonus after 90 days of employment $500 additional bonus after 180 days of employment $1000 additional bonus after 365 days of employment $750 referral bonus after 6 months Basic Qualifications Must be 18 years of age Must be cleared on any background screening English literacy Ability to use a calculator and a tape measure. Computer skills a plus Must be able to lift up to 40 pounds. Must be able to stand, walk, sit; use hands and fingers to handle or feel; and reach with hands and arms. Why should you join our team? Our amazing environment keeps safety as its top priority! You can enjoy a collaborative atmosphere in a clean and climate-controlled facility. Our core values are how we thrive, and you will get to work with people who share them: Organizational Pride, Highest Ethical Standards, Quality You Can Trust, Collaboration, Entrepreneurship, and Continuous Improvement. Our opportunities to advance give any qualified associate the opportunity to move to a higher level job. Our on-the-job training and skills development will ensure your success in your job. If you are interested in becoming a part of a World-Class Team, submit your application today! ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: Coordinate and oversee corrective and preventive action activities across manufacturing operations. Track, document, and maintain corrective action records in accordance with company requirements. Ensure timely closure of corrective action tasks and verify effectiveness of solutions. Lead investigations into product or process non-conformances. Facilitate problem-solving sessions using tools such as 5 Whys, Fishbone Diagrams, and FMEA. Collaborate with engineering, production, and quality teams to identify systemic issues. Create or revise work instructions or procedures to support improvement actions. Technical writing ability and knowledge of document & configuration control. Prepare reports and summaries of corrective action status. Support internal and external audits by providing corrective action documentation and objective evidence. Recommend process improvements to reduce defects, scrap, and rework. Provide training and guidance to employees on corrective action and best practices. Monitor trends in non-conformances and proactively address recurring issues. Perform quality system and process audits. Perform product inspections and nonconformance dispositions. Experience with QT9 QMS a plus. All other relevant duties as assigned by supervisor QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Additionally, the Quality Technician must have proven root cause problem-solving experience, attention to detail & documentation accuracy; cross-functional collaboration & analytical thinking with a continuous improvement mindset. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions RESPONSIBILITIES OF THIS POSITION: 3-5 years of experience in manufacturing quality assurance or corrective action coordination. Strong knowledge of CAPA processes, ISO 9001, Lean, and Six Sigma methodologies. Excellent organizational, communication, and facilitation skills. Proficiency in quality tools and software for managing & tracking corrective actions & tasks. Ability to assess adequacy of objective evidence to approve and close corrective actions. Strong knowledge of ISO 9001, Lean Manufacturing, and Six Sigma principles. Excellent leadership, communication, and problem-solving skills. Proficiency in quality tools (SPC, FMEA, control plans, etc.) Working experience with Microsoft programs: MS Word, Power Point, Visio, Excel, Outlook. Strong aptitude for learning software and managing data. Demonstrated people and leadership skills, including conflict resolution, problem solving, and performance management. Excellent organizational skills, attention to detail, and the ability to work with staff from diverse disciplines and backgrounds. Other duties as assigned PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand. The employee frequently is required to use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to walk and sit. The employee is occasionally required to stand, stoop and/or kneel. The employee must regularly lift and/or move up to 25 pounds and occasionally lift and/or move up to 60 pounds, with assistance if necessary. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and ability to adjust focus.

Job Description Hourly Rate: $24.00 - $29.00 (Based on Experience) Benefits Offered: 401K, Life, Dental, Medical, Vision Shift: 1st Shift: Monday - Friday 7:00 am to 5:00 pm We are seeking a driven and detail-oriented Quality Control Technician who is committed to building a long-term career in Quality. This role is well-suited for individuals with foundational experience in manufacturing or inspection who take pride in precision, integrity, and continuous improvement. The Quality Control Technician reports directly to the Quality Manager and plays a vital role in maintaining the integrity of our products, processes, and documentation. You will perform inspections, maintain quality records, support root cause analysis, and collaborate with production teams to uphold ISO 9001 and customer requirements. Key Responsibilities: • Conduct thorough inspections of products and assemblies to verify compliance with specifications and quality standards. • Monitor the effectiveness of quality control processes and support improvements within assigned areas. • Document inspection findings accurately and maintain complete, organized quality records. • Assist in investigations of non-conformances, contributing to root cause analysis and corrective actions. • Collaborate with production teams to identify issues early and resolve quality concerns efficiently. • Follow established ISO 9001 procedures and support the ongoing development of the Quality Management System. • Participate in internal audits and support readiness for customers or third-party audits. • Uphold a high level of professionalism and represent the Quality department with integrity in all interactions. Qualifications: • 1-3 years of experience in manufacturing, inspection, or quality-related work. • High School Diploma or equivalent required; technical training or an associate degree is preferred. • Strong attention to detail with a natural ability to notice small inconsistencies or defects. • High personal integrity - consistently doing the right thing, even when it is inconvenient • solid communication skills, both written and verbal, with the ability to collaborate across departments • proficiency in Microsoft Office Suite; familiarity with quality management software is a plus • Strong organizational skills and the ability to maintain accurate, reliable documentation • A proactive problem-solver who can follow detailed processes, manage multiple tasks, and work with minimal supervision.

Are you passionate about ensuring compliance and protecting our environment? As a Quality Technician, you will play a vital role in monitoring and documenting environmental conditions at project sites. Your keen observations and meticulous tracking will not only help us adhere to environmental agency regulations but also mitigate potential liabilities. Collaborate with industry experts and committed teams to ensure our projects are environmentally responsible and sustainable! Apply now and transform your career with us. What you will be doing Assists with identifying risks and discrepancies at the project site during daily site walks. Documents findings, evaluations, and inspections using Company-prescribed procedures and software. Documents, analyzes, and reports environmental performance to internal and external clients and regulatory bodies. Supports impact assessments to identify, assess, and reduce the organization's environmental risks and financial costs, following the direction of the environmental team and procedures. What we are looking for High school diploma / GED required. Environmental certification required. Experience or training in environmental regulatory and construction industry compliance preferred. Strong organization and communication skills. Willingness and ability to learn and grow in environmental monitoring, technical writing and documentation. Why work for us Some of the benefits you may be eligible for as an employee are: Comprehensive compensation package and paid time off program Industry leading 401(k)/RRSP Medical/Extended Health Care, Dental, Vision and/or Provincial Medical Wellness benefits & Employee Assistance Program Tuition Reimbursement Program We are an EEO/ADA/Veterans employer. Salary Min USD $55,000.00/Yr. Salary Max USD $65,000.00/Yr. Vehicle Program Company Vehicle

About Us Apollo is a Mission-Critical Infrastructure Engineering, Construction, Commissioning, and Operations Support Services Company. We serve mission-critical industries globally with commissioning, emergency response, operations support, and owner's representative services. Apollo is currently executing projects in multiple states in the United States, in Canada and Brazil. Since our inception, we have built a commissioning firm based on trust, one relationship at a time. We hire the best people who can handle critical systems, love challenges, and thrive in a dynamic environment. We focus on understanding each client's needs and are relentless in meeting them. Job Description The Data Center Construction QAQC Co-Op Engineer (CxE-C) provides construction management, quality assurance and quality control support during the delivery of mission-critical data center facilities. They also participate in the supply chain coordination, inspection and validation of mechanical and electrical components, ensuring that delivered components meet the required specifications before installation and commissioning. The QAQC-C partners with senior team members, project managers, construction contractors, equipment vendors, and client staff to monitor and ensure adherence to project specifications, quality standards and timelines throughout the construction process. The QAQC-C provides construction support as part of Apollo's onsite, client-facing teams. Thus, this role may involve approximately 75% or more travel to various client locations. Education Relevant coursework towards a bachelor's or associate degree in engineering, construction management, supply chain & logistics, or a related discipline OR One year of experience in the supply chain coordination, inspection, validation, and quality control of mechanical and/or electrical systems in a construction environment. Key Responsibilities Support the review of construction plans and design specifications to help identify quality and compliance requirements. Collaborate with project managers and suppliers to ensure timely delivery and installation of electrical and mechanical components. Work with the QAQC team to identify and address potential risks or areas for improvement during project execution. Help prepare and maintain detailed documentation of inspections, tests, and quality reports for project teams. Conduct pre-installation inspections under the guidance of senior QAQC team members. Achieve certification for NFPA70E, OSHA 30, and other training as required. Travel to other project locations as required. Perform other duties as assigned. Physical Demands The following physical demands must be met to successfully perform the essential functions of this role. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions: Frequently manipulating, moving, or grasping small parts, devices, or tools. Frequently required to remain in a stationary position. Frequently moving through office areas, critical facilities and other environments, including tight and confined spaces. Exposure to low/high temperatures and outdoor elements such as precipitation and wind. Working and walking on different types of terrain on active construction sites (e.g., concrete flooring, gravel, unpaved roads). Frequently ascending and descending stairs and ladders to access equipment. Frequently positioning oneself under or over equipment. Frequently moving equipment weighing up to 50 pounds. Qualifications Basic knowledge of mechanical and electrical systems in construction Strong communication and collaboration skills to work with cross-functional teams, including project managers and contractors Skilled at using MS Office tools. Ability to analyze and prepare reports and technical documents. Ability to work under pressure and meet critical deadlines. Must be detail oriented. Prerequisites for Employment: Successful Background Check including pre-employment drug screening US citizens, permanent residents or any candidate with eligibility to work in the US Graduating in May 2027 or later Apollo challenges the brightest, most talented, and driven individuals in the industry by providing an environment that embraces initiative, diversity, and achievement. We are an Equal Employment Opportunity, Affirmative Action employer supporting women, minorities, veterans and people with disabilities. We participate in the Department of Homeland Security E-Verify program.

TempToFT Testing Solder Paste batches in the lab. Will also be handling packing slips, BOL and sometimes dealing with shipping companies. Must have Microsoft Office experience, Excel, Word. Looking for someone that will be punctual in attendance and deadlines. Must be a team player. 1965 Evergreen Blvd. , Suite 400, Duluth, GA 30096, United States of America

Your activities Communicates with internal customers to resolve any quality-related issues. Drive investigation and corrective action processes to resolve quality issues, collaborating with programmers and operators during production to determine effective resolutions, including butnot limited to: Ensuring proper measuring equipment is available to produce every part. Ensuring all measuring equipment is always calibrated. Documenting critical features of a first article (the first item or unit produced in a manufacturing cycle) Communicating to machine programmers and/or operators how to proceed post-investigation. As needed, re-train operators, as needed (e.g., measuring equipment training, parts inspection training, or other critical quality topics). Document all quality incident issues and corrective action. Takes administrative steps to revises and implements standard processes and procedures, including applicable documentation for manufacturing departments. Oversee measurement equipment processes, including selecting appropriate gauging for production parts, ensuring calibration, and training operators on their proper use. Conducts first article inspections and random inspections as required, ensuring ongoing compliance and that employees are properly trained. Identify critical features for first article inspections and train operators on inspection procedures. Trains and supports manufacturing employees with best practices in quality inspection and documentation. Maintain and manage all documentation related to equipment, training, inspections, and quality processes. Align all quality procedures and documentation standards according to ISO9001 standards, and in alignment with WIKA standards and procedures. Suggests areas and equipment for improvement opportunities. Complete other related duties, as assigned. Your profile 5 years' experience in a machine shop environment within a manufacturing company Technical knowledge of manufacturing equipment and techniques. Demonstrated experience with a wide range of measurement equipment (e.g. various types of calipers and micrometers, hardness testers, gauge blocks, plug and ring gauges, visual measuring systems etc.) Demonstrable grasp of mathematics Inclinations toward thoroughness and precision Strong analytical and mechanical skills. Team-oriented individual. Technical reading comprehension, including understanding and reading of engineering drawings is required. Geometric Dimensioning and Tolerancing (GD&T) preferred Knowledge of quality systems (ISO 9001) Comprehensive knowledge of lean improvement methodology is a plus. Excellent communication skills. Strong computer skills including Microsoft Office Suite, particularly Excel, machine shop systems, CAD drafting, ERP, and other related computer skills Experience in problem solving techniques (e.g. 5 Whys,

Job Description The Sr. Quality Control (QC) Technician will play a critical role in planning/coordinating testing and inspection activities related to company products, and recording, analyzing and approving results during product development and manufacturing. The Sr. QC Technician is also responsible for environmental monitoring and contamination control activities. The ideal candidate is a highly versatile and meticulously detail-oriented individual with a quality control background and a strong foundation in Microbiology. This is a full-time, on-site position. Key Responsibilities: Technical: Plan, perform and report inspection & routine testing of incoming materials, utilities, products (intermediate and finished), and validation samples. Coordinate, plan, and collect environmental monitoring (EM) samples of production areas and utilities. Release of incoming (raw) materials. Coordinate with external test laboratories and sterilization facility for sample submission, testing, processing, and reporting of results. Implement and maintain QC databases, to ensure that relevant information is up to date and accessible to relevant functions. Initiate and/or review Quality Indicators (Qis), including, but not limited to, deviations and out of specification (OOS) reports related to QC activities. Coordinate, plan and perform equipment calibration and maintenance activities for QC equipment. Participate in product development and risk management activities, as needed. Train existing and new QC personnel, as required. Coordinate and plan Quarterly Dose Audits (QDA). Support test method, process, cleanroom, and equipment validation activities. Inspect product labels. Review and verify batch production records, QC testing data, and logbooks for accuracy, completeness, and compliance with internal procedures prior to product release recommendations. Maintain of equipment, production, and other quality records, as needed. Quality Management System (QMS): Support development and maintenance of quality control procedures and related documentation, including but not limited to specification documents and testing procedures. Understand relevant quality control requirements. Suggest possible improvements to current testing and identify needs for changes in the Quality Management System. Assist the CAPA Process Owner investigating and resolving non-conformances. Assist the CAPA Process Owner, ensuring thorough root cause analysis and effective corrective actions. Support internal, supplier, and external regulatory audits (FDA, Notified Bodies), as needed. Safety/Organizational/Productivity: Know, understand and adhere to all safety standards, i.e., emergency preparedness, chemical, infectious agents and radioactive hazards. Participate in the introduction and evaluation of new procedures, supplies and equipment to the extent necessary for proper and safe performance of work activities. Ensure proper training of colleagues, as necessary. Use resources (equipment, disposables, time) in a responsible, cost-effective manner. Ensure QC laboratories are clean and organized. Qualifications: Education: Bachelor's degree in microbiology, biology, life science, or a related field. Experience: Minimum 3 years of experience in quality control in the medical device industry or contract laboratories. Applicable knowledge of ISO 13485, 21 CFR Part 820, and other applicable medical device regulations. Working knowledge of MRP or MES systems, preferably in Microsoft Dynamics 365. Experience working in laboratory and cleanroom settings. Proficient in using quality management software and tools. Experience with analytical instruments. Skills: Strong attention to detail and ability to follow precise work instructions. Adaptability to changes in priorities and exceptional time management to meet deadlines. Work well independently, as well as being able to work cooperatively in a team of professionals with commitment to collaborative problem-solving and the ability to maintain professional working relationships under pressure. Effective communication and presentation. Willingness to mentor other team members and share knowledge. Proactively seeking information, tools or assistance needed to resolve a problem or resolve a task. Detail-oriented ability to observe, investigate, and analyze data and identify a defect or a failure. Strong foundation of contamination control, aseptic techniques, and microbiological testing is highly desired. Travel Requirement: Ability to travel domestic and international Pay Range$54,000-$64,100 USD Physical Requirements and Work Conditions The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions. Mobility & Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping. Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role. Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment. Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver's license. Specific requirements may vary by role. Contact an HR representative for details related to the position. Our credentials Kuros is a Swiss-headquartered biotech company, listed on the SIX Swiss Stock Exchange since 2016 (under symbol KURN). With additional operations in the Netherlands and the USA, we continue to grow our global team. To deliver the ideal bone graft, you need the highest quality and quantity of scientific evidence behind it. We believe that this is a key differentiator for Kuros, given the urgent need to advance bone healing. Listing on the SIX Swiss Exchange under the symbol KURN since 2016 A commercial & research footprint that spans >20 markets Dozens of clinical and scientific expert Advisers >25 orthobiologics-related patents >400 patients evaluated in Level I, randomized controlled clinical trials >20 well-controlled Level I-IV clinical trials initiated, including 6 that are complete1 Published Level I evidence published in Spine Kuros Biosciences is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: This job requires a U.S. Person. A U.S. Person is a lawful permanent resident as defined in 8 U.S.C. 1101(a)(20) or who is a protected individual as defined by 8 U.S.C. 1324b(a)(3). U.S. citizens, U.S. nationals, U.S. permanent residents, or individuals granted refugee or asylee status in the U.S. are considered U.S. persons. For a complete definition of “U.S. Person” go here. ********************************************************************************************** Security Clearance: None/Not Required Joining Collins Aerospace isn't just about finding a job; it's about embarking on a journey to redefine the future of aerospace technology. Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market. Collins Aerospace is seeking a detail-oriented and proactive Quality Technician to join our team in support of the G400 Flight Test program. Based at our customer facility in Savannah, GA, this onsite, mid-shift role plays a critical part in upholding the highest standards of quality and compliance across our products and processes. The ideal candidate brings a strong commitment to precision, collaboration, and continuous improvement within a fast-paced aerospace environment. This position is working onsite at Gulfstream facilities in Savannah, GA. This position is a mid-shift role (Monday - Friday , 10 am - 6:30 pm) Relocation assistance will be provided. What You Will Do Conduct in-process and final inspections of products and materials Perform post-flight inspections, and report results directly to the customer Document inspection results and maintain detailed records Identify, report, and assist in the resolution of quality issues Interpret technical drawings, specifications, and standards Use measurement tools and equipment accurately Work closely with production and engineering teams to ensure quality requirements are met Apply fundamental math skills, including addition, subtraction, multiplication, division, fractions, and percentages, to perform accurate measurements and calculations. Support materials handling, including chemicals and parts receiving and inspection An essential function is to see and read information on multiple monitors and type on a color-coded keyboard for eight or more hours of the day. You will be required to pass a vision assessment. Occasional work overtime/ weekend shift work as needed Utilize strong written and verbal communication skills on a day-to-day basis. Bring high energy, enthusiasm, and a positive attitude to your work, demonstrating strong self-motivation, initiative, and a focus on driving results. Promote a culture of continuous improvement and attention to detail This role requires performing detailed visual inspections for extended periods, including identifying defects and interpreting color-coded indicators. You will be required to pass a vision assessment to ensure you meet the necessary visual acuity and color vision standards for this work. Safely perform other duties as assigned Qualifications You Must Have Typically requires an AA/AS degree (or other 2-year post high school training) with a minimum of 6 years of relevant experience. 3+ years in an Aerospace or similar inspection role using inspection tools/techniques and measuring equipment (e.g., calipers, micrometers, gauges) 3 years of experience in reading blueprints (2D and 3D) and interpreting specifications Experience in navigating and operating CATIA, Word, Excel, PowerPoint, and ERP programs Qualifications We Prefer SAP Experience Experience in AS9100 and AS9145 Experience in Aerospace / Automotive Industries What We Offer Some of our competitive benefits package includes: Medical, dental, and vision insurance Three weeks of vacation for newly hired employees Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option Tuition reimbursement program Student Loan Repayment Program Life insurance and disability coverage Optional coverages you can buy pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection Birth, adoption, parental leave benefits Ovia Health, fertility, and family planning Adoption Assistance Autism Benefit Employee Assistance Plan, including up to 10 free counseling sessions Healthy You Incentives, wellness rewards program Doctor on Demand, virtual doctor visits Bright Horizons, child and elder care services Teladoc Medical Experts, second opinion program And more! Learn More & Apply Now! Our Advanced Structures team leverages advanced materials and additive manufacturing to develop complex interior and exterior solutions. These solutions ensure structural integrity of the aircraft, help aircraft take off and land, stay trim in the air, move forward, carry cargo and conduct rescues. We delight our customers with superior products and best-in-class service. Our global team is committed to continuous improvement - we work hard to make our solutions lighter-weight, stronger and more technically advanced, so that plane travel can be safer, more affordable and more sustainable in the years to come. We are looking for the best and brightest to fly and land with us! WE ARE REDEFINING AEROSPACE. *Please ensure the role type (defined below) is appropriate for your needs before applying to this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world - and access to Collins sites when their work requires in-person meetings. At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. The salary range for this role is 50,000 USD - 100,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

medmix is a global leader in high-precision delivery devices, with leading positions in healthcare, consumer and industrial end-markets. Our customers benefit from our dedication to innovation and technological advancement that has resulted in over 900 active patents. Our 15 production sites worldwide together with our highly motivated and experienced team of nearly 2'700 employees are at service of our customers with uncompromising quality, proximity and agility. medmix is headquartered in Baar, Switzerland. Our shares are traded on the SIX Swiss Exchange (SIX: MEDX). We are looking for a Quality Technician to join us at medmix, at our new Greenfield Site outside of Atlanta, Georgia USA. This exciting opportunity will allow you use your skills to identify areas of improvement and propose recommendations to management. You will lead and drive the implementation of your recommendations and assess its impact to the business. If you are eager to learn, strive for personal development, are highly motivated and organized, and a great communicator, you can help us drive medmix to the next level. Job Description Job purpose Responsible for assisting with the implementation, management, and administration of the quality management system and ensuring products are manufactured per quality and regulatory requirements and industry best practices. Main Accountabilities and tasks May participate in “on the floor” audits of production personnel to ensure adherence to procedures and training effectiveness Conducts sampling, product testing, and visual inspection of components and/or finished goods; identifies nonconformances, if any, and ensures proper containment as required Completes accurate, timely, and legible documentation of all inspection/testing data Participates in weekly production walk-throughs to ensure quality compliance Engage in Safety, Quality, Production, and Plant related programs as required (Safety Observations, Meetings, Gembas, etc.) Participates in continuous improvement objectives to assure compliance with regulations Performs other duties as assigned by management Maintain and apply knowledge of current policies, regulations, and industrial processes for medmix USA Maintains quality records procedure and coordinates non-conformance reporting Compiles, analyze, and interprets statistical data related to quality operations May be required to cover position on their assigned shift due to absences for vacations, leave, etc. Perform all other miscellaneous duties as appropriately directed by Quality Management or designate Qualifications Desired experience and qualifications Work Experience: 1-3 years of experience in a regulated workplace preferred Education: Bachelor's degree preferred or equivalent with education and experience. Other: Experience with injection molding processes, parameters, and troubleshooting is preferred. 1-3 years of experience in a quality role preferred. Proficiency in personal computers, especially word processing software, spreadsheets, presentation, and database software. Ability to learn quickly and maintain the Quality Assurance metrics Knowledge of ISO standards or the ability to quickly learn and retain knowledge as required for system compliance Ability to perform work accurately and thoroughly and to work independently with minimal supervision Must be organized and can follow a systematic method of performing tasks and the ability to organize and direct a project to completion Must be self-directed and motivated to optimally utilize the available time to organize and complete expected work within given deadlines and reasonable work schedules Communication skills, both oral and written, as required to communicate effectively with others at all levels in the organization and to provide clear and concise reports and policies as needed. Ability to effectively present information publicly Ability to work well with subordinates, peers and superiors in all departments. Additional Information Benefits we offer: An innovative, vibrant and agile culture Growth opportunities in a globally successful and dynamic business on a growth trajectory Excellent employee benefits including Twelve (12) company paid holidays per year Medical, dental, vision, Life/AD&D, Short- and Long-Term Disability medmix Employee Savings Plan / 401k with 100% employer match up to 6% of your annual base salary Eligible to receive additional non-elective 401k contributions on a quarterly basis Employee Assistance Program Access to a wide range of discounts on shopping, entertainment and lifestyle Years of Service Awards medmix is an equal opportunity employer, committed to the strength of a diverse workforce. 93% of our employees would go above and beyond to deliver results - do you have the drive to succeed? Join us and boost your career, starting today!

We exist to put camera gear in the hands of ordinary people to unlock extraordinary potential. The original camera re-commerce company, KEH has always envisioned a better way to support the passion and profession of photography. Serving the camera community since 1979, KEH has become the largest curated market for field-tested, expert-graded photo and video equipment in the industry. At KEH Camera, we're passionate about making photography and videography accessible and sustainable by buying and selling pre-owned camera gear. We are the go-to resource for everyone looking for photo or video gear, offering high-quality KEH Certified equipment at great prices while extending the life of gear for a global community of creatives. Why Work at KEH Camera? Be Part of the Fastest Growing Company Driving the Societal Explosion of Images and Video: Join a company that's not just in the business of gear fueling creativity, empowering photographers and videographers, and shaping the future of images and videos. Whether you have a passion for the craft or the gear or neither, if you have inner passion for something you will find a home here! Collaborate with Visionaries: Work alongside a team of passionate, dedicated individuals who live and breathe KEH and all that it stands is about. At KEH, innovation and growth aren't just goals, they're part of our DNA. Your ideas and contributions will be valued from day one. Make a Real Impact: At KEH, you're more than just an employee; you're a key player in an exciting, ever-evolving industry, and a part of a special and rapidly growing company. Your work here directly influences an industry, as well as the lives and joys of countless people, and helps shape the future of the photo and video gear marketplace. A Culture of Creativity and Learning: We support your personal and professional growth with continuous learning, training, and career advancement opportunities. Whether you're a photography enthusiast, a tech expert, or a truly curious person, we'll help you grow your skills and expertise. Join KEH Camera - Where Gear Gets a Second Life and Your Career Takes Off Are you passionate about photography, fascinated by how things work, or simply love hands-on, detail-oriented work? KEH Camera is looking for motivated individuals to join our team as Camera Quality Inspection Technicians. This is a great opportunity to turn your curiosity into a career - no prior experience required, just a willingness to learn and grow. Location On-site Smyrna, GA Starting Pay: $15.00 per hour, with advancement opportunities and performance-based incentives What You Will Do: As a Camera Quality Inspection Technician, you'll help evaluate incoming photographic gear - from digital cameras to vintage film models - ensuring everything meets our high quality standards before it reaches our customers. You'll receive thorough on-the-job training and be supported every step of the way as you develop valuable technical skills. Your key responsibilities will include: Inspect and test various photographic equipment, including digital, 35mm, medium format, and large format cameras, as well as lenses and accessories. Identify functional or cosmetic issues such as haze, dust, fungus, scratches, or mechanical faults. Grade equipment based on KEH's standardized quality scale. Record and document all findings accurately in our internal systems. Collaborate with Receiving and Sorting teams to maintain workflow and quality standards. Maintain a clean, organized workspace and handle all tools and equipment with care. Why You'll Love This Role Clear Path for Growth: Advance to Junior Technician in as little as 6 months - with a pay increase to $16.00/hour upon qualification. Productivity Incentives: Earn up to an additional $4.00/hour based on performance and efficiency. Hands-On Learning: No prior technical or photography experience is required - just a passion for learning and working with your hands. Career Development: Eligible for our Apprenticeship Program within the Technical Department, giving you access to structured training and real career advancement. Skills Needed to be Successful: A strong attention to detail and the ability to stay focused on repetitive tasks. A natural curiosity or interest in how mechanical or electronic devices work - photography interest is a plus! Willingness to learn new skills in a supportive, hands-on environment. Ability to follow instructions carefully and document findings clearly. Professional communication skills and a collaborative mindset. Comfort working while seated or standing for long periods, and using small tools with care. Bonus if you have: Experience with electronics, camera equipment, or quality control - but not required. Language Skills: Must have a basic command of the English language, including the ability to read, write, and understand simple instructions. Work Hard, Play Hard: Enjoy a hard-working and fast-paced environment where your work is celebrated and where you can commit your energy and efforts alongside like-minded individuals who are focused on building and growing a great company and winning. Physical Demands: Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to talk or hear. The employee is occasionally required to stand, walk, twist, bend, sit, use hands, handle, or feel objects, tools, or controls, and reach with hands and arms. Ability to lift 40lbs. May be required to lift overhead. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The noise level in the work environment is usually moderate. Benefits: Comprehensive medical, dental, and vision plans HAS and FSA Accounts Short and Long term disability Company provided life insurance 401(k) and company match Paid vacation, sick days and holiday Options for Pet Insurance and Legal Services Discounts of camera gear Equal Opportunity Employer: KEH Camera is an Equal Opportunity Employer that does not discriminate on the basis of any status protected under federal, state, or local law. Applicants will be considered regardless of their sex, race, age, religion, color, national origin, ancestry, physical disability, mental disability, medical condition (associated with cancer, a history of cancer, or genetic characteristics), HIV/AIDS status, genetic information, marital status, sexual orientation, gender, gender identity, gender expression, military and veteran status, or other protected category under the law based on race, color, religion, sex, age, sexual orientation, gender identity and/or expression, national origin, veteran status or disability in relation to our recruiting, hiring, and promoting practices. The statements contained in this position description are not necessarily all-inclusive; additional duties and responsibilities may be assigned, and requirements may vary from time to time. Professional business references and a background screening will be required for all final applicants selected for a position. If you need assistance or an accommodation due to a disability, you may contact ***************. KEH Camera is not currently accepting resumes from agencies for this position. If you are a recruiter, search firm, or employment agency, you will not be compensated in any way for your referral of a candidate, even if KEH Camera hires the candidate.

Company: Fusion Medical Staffing Job Details Fusion Medical Staffing is seeking a skilled Cath Lab Tech for a 13-week travel assignment in Atlanta, Georgia. As a member of our team, you'll have the opportunity to make a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team. Required Qualifications: One year's recent experience as a Cardiac Cath Lab Tech Current BLS (AHA/ARC) certification ARRT, RCES, or RCIS certification Current ACLS (AHA/ARC) certification Preferred Qualifications: Valid Radiologic Technologist license in compliance within state regulations PALS (AHA/ARC) or ENPC Certifications Other certifications and licenses may be required for this position Summary: The Cath Lab Technologist is responsible for assisting in diagnostic and interventional cardiovascular procedures in the cardiac catheterization lab. This role involves preparing patients and equipment, monitoring hemodynamic data, assisting physicians during procedures, and ensuring patient safety throughout the process. The technologist operates specialized imaging equipment, maintains sterile technique, and collaborates with the healthcare team to provide high-quality patient care. This position requires technical expertise in cardiovascular procedures, critical thinking skills, and the ability to work efficiently in high-pressure situations. Essential Work Functions: Prepare and position patients for cardiac catheterization, angioplasty, stent placement, electrophysiology studies, and other interventional procedures Assist physicians during procedures by passing catheters, wires, balloons, and stents, and operating fluoroscopy and hemodynamic monitoring equipment Operate and maintain imaging equipment, contrast injectors, and hemodynamic monitoring systems, ensuring proper functionality Scrub in and assist with sterile field setup, ensuring adherence to infection control and procedural protocols Perform sheath removal and hemostasis using manual compression or closure devices as directed Maintain accurate documentation, including patient records, imaging data, and equipment logs Assist with inventory management, stocking supplies, and ensuring proper storage of sterile instruments and medications Adhere to radiation safety protocols, ensuring proper use of lead aprons, shields, and dosimeters Ensure compliance with hospital policies, safety guidelines, and regulatory requirements Adhere to hospital safety protocols, infection control guidelines, and regulatory standards Perform other duties as assigned within the scope of practice Required Essential Skills: Critical thinking, service excellence, and good interpersonal communication skills The ability to read, write, and communicate in the English language Ability to read/comprehend written instructions, follow verbal instructions, and proficiency in PC skills Physical Abilities - Must be able to remain in a stationary position, move about, move equipment (50-100lbs), push, pull, and bend Interpersonal Skills - Must be able to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and professionalism Technical/Motor Skills - Must have the ability to grasp, perform fine manipulation, push/pull, and move about when assisting with procedures and/or using department equipment Mental Requirements - Must be able to cope with frequent contact with the general public and customers while meeting deadlines under pressure. Must be able to work under close supervision occasionally, as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail Sensory - Must possess visual acuity and ability to effectively communicate Benefits Include: Highly competitive pay for travel professionals Comprehensive medical, dental, and vision insurance with first day coverage Paid Time Off (PTO) after 1560 hours Life and Short-term disability offered 401(k) matching Aggressive Refer-a-friend Bonus Program 24/7 recruiter support Reimbursement for licensure and CEUs Why Choose Fusion? At Fusion Medical Staffing, our goal is to improve the lives of everyone we touch, and we're always looking for people like you to join our mission. Your passion for helping others deserves a partner just as committed to supporting you - that's why we offer day one insurance, $0 copay for mental health services, scholarships and awards, exclusive discounts, and more. From your personal recruiter to our clinical and traveler experience teams, we're here to guide and celebrate you along your journey. You take care of others; we take care of you. Other Duties Disclaimer: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned. This job description is not a comprehensive list of all activities, duties, or responsibilities that are required of the employee for this job and is subject to change at any time with or without notice. Start your rewarding career as a Travel Cath Lab Tech with Fusion Medical Staffing and join our mission to improve lives. Apply now! *Fusion is an EOE/E-Verify Employer #pb11

Join our team to play a pivotal role in mitigating tech risks and upholding operational excellence, driving innovation in risk management. As a Tech Risk & Controls Lead in the Cybersecurity and Technology Controls ogranization, you will be responsible for identifying, and mitigating compliance and operational risks in line with the firm's standards. You will also provide subject matter expertise and technical guidance to technology-aligned process owners, ensuring that implemented controls are operating effectively and in compliance with regulatory, legal, and industry standards. By partnering with various stakeholders, including Product Owners, Business Control Managers, and Regulators, you will contribute to the reporting of a comprehensive view of technology risk posture and its impact on the business. Your advanced knowledge of risk management principles, practices, and theories will enable you to drive innovative solutions and effectively manage a diverse team in a dynamic and evolving risk landscape. Job responsibilities Drives efficient and effective execution of assessments, ensuring alignment with organizational objectives, risk appetite, and regulatory compliance Leads the governance of issues raised from assessments, tracking concerns, and resolution of findings Ensures timely and effective closure of identified control deficiencies Provides subject matter expertise in regulatory assessments, ensuring that the organization adheres to applicable frameworks such as HITRUST and other relevant standards Ensures effective identification, quantification, communication, and management of technology risk, focusing on root cause analysis and resolution recommendations Develops and maintains robust relationships, becoming a trusted partner with LOB technologists, assessments teams, and data officers to facilitate cross-functional collaboration and progress toward shared goals Executes reporting and governance of controls, policies, issue management, and measurements, offering senior management insights into control effectiveness and inform governance work Proactively monitors and evaluate control effectiveness, identify gaps, and recommend enhancements to strengthen risk posture and regulatory compliance Required qualifications, capabilities, and skills 5+ years of experience or equivalent expertise in technology risk management, information security, or related field, emphasizing risk identification, assessment, and mitigation Experience with risk management frameworks such as HITRUST, industry standards such as HIPAA, and financial industry regulatory requirements (SOX, PCI, ISO 270001, NIST, GLBA, NYDFS) Proficient knowledge and expertise in data security, risk assessment & reporting, control evaluation, design, and governance, with a proven record of implementing effective risk mitigation strategies Demonstrated ability to influence executive-level strategic decision-making and translating technology insights into business strategies for senior executives Preferred qualifications, capabilities, and skills CISM, CRISC, CISSP, or similar industry-recognized risk and risk certifications are preferred Experience managing projects within Cybersecurity Technology, Risk, and Controls

Job Description Who is Habasit? Habasit is the global leader in the manufacturing of lightweight conveyor belting. Our slogan “Solutions in Motion” defines us; we are a provider of world class power-transmission and conveying solutions. At Habasit, we understand that a global leader is only as good as the people who represent it, and we are always searching for the right people to keep us in motion. We are looking for ambitious individuals, leaders, and students who are ready to help move us forward. If you have a can-do attitude and want to join a world-class organization, read on and apply today! SUMMARY The Quality Technician is primarily responsible for managing and driving root cause and corrective actions within the manufacturing & business environment. This role ensures that product and process nonconformities are properly investigated, documented, and resolved in compliance with company procedures. The Quality Technician partners with cross-functional teams to identify root causes, implement effective solutions, and monitor results to prevent recurrence. This role is ideal for someone who thrives on problem-solving, compliance, and driving accountability across teams. Things you should know about Habasit's opportunities: Direct hire opportunity Eligible for bonuses and incentives $500 bonus after 90 days of employment $500 additional bonus after 180 days of employment $1000 additional bonus after 365 days of employment $750 referral bonus after 6 months Basic Qualifications Must be 18 years of age Must be cleared on any background screening English literacy Ability to use a calculator and a tape measure. Computer skills a plus Must be able to lift up to 40 pounds. Must be able to stand, walk, sit; use hands and fingers to handle or feel; and reach with hands and arms. Why should you join our team? Our amazing environment keeps safety as its top priority! You can enjoy a collaborative atmosphere in a clean and climate-controlled facility. Our core values are how we thrive, and you will get to work with people who share them: Organizational Pride, Highest Ethical Standards, Quality You Can Trust, Collaboration, Entrepreneurship, and Continuous Improvement. Our opportunities to advance give any qualified associate the opportunity to move to a higher level job. Our on-the-job training and skills development will ensure your success in your job. If you are interested in becoming a part of a World-Class Team, submit your application today! ESSENTIAL DUTIES AND RESPONSIBILITIES include the following: Coordinate and oversee corrective and preventive action activities across manufacturing operations. Track, document, and maintain corrective action records in accordance with company requirements. Ensure timely closure of corrective action tasks and verify effectiveness of solutions. Lead investigations into product or process non-conformances. Facilitate problem-solving sessions using tools such as 5 Whys, Fishbone Diagrams, and FMEA. Collaborate with engineering, production, and quality teams to identify systemic issues. Create or revise work instructions or procedures to support improvement actions. Technical writing ability and knowledge of document & configuration control. Prepare reports and summaries of corrective action status. Support internal and external audits by providing corrective action documentation and objective evidence. Recommend process improvements to reduce defects, scrap, and rework. Provide training and guidance to employees on corrective action and best practices. Monitor trends in non-conformances and proactively address recurring issues. Perform quality system and process audits. Perform product inspections and nonconformance dispositions. Experience with QT9 QMS a plus. All other relevant duties as assigned by supervisor QUALIFICATIONSTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Additionally, the Quality Technician must have proven root cause problem-solving experience, attention to detail & documentation accuracy; cross-functional collaboration & analytical thinking with a continuous improvement mindset. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions RESPONSIBILITIES OF THIS POSITION: 3-5 years of experience in manufacturing quality assurance or corrective action coordination. Strong knowledge of CAPA processes, ISO 9001, Lean, and Six Sigma methodologies. Excellent organizational, communication, and facilitation skills. Proficiency in quality tools and software for managing & tracking corrective actions & tasks. Ability to assess adequacy of objective evidence to approve and close corrective actions. Strong knowledge of ISO 9001, Lean Manufacturing, and Six Sigma principles. Excellent leadership, communication, and problem-solving skills. Proficiency in quality tools (SPC, FMEA, control plans, etc.) Working experience with Microsoft programs: MS Word, Power Point, Visio, Excel, Outlook. Strong aptitude for learning software and managing data. Demonstrated people and leadership skills, including conflict resolution, problem solving, and performance management. Excellent organizational skills, attention to detail, and the ability to work with staff from diverse disciplines and backgrounds. Other duties as assigned PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand. The employee frequently is required to use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to walk and sit. The employee is occasionally required to stand, stoop and/or kneel. The employee must regularly lift and/or move up to 25 pounds and occasionally lift and/or move up to 60 pounds, with assistance if necessary. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and ability to adjust focus. Daily - 8:00AM-5:00PM - Monday through Friday

medmix is a global leader in high-precision delivery devices, with leading positions in healthcare, consumer and industrial end-markets. Our customers benefit from our dedication to innovation and technological advancement that has resulted in over 900 active patents. Our 15 production sites worldwide together with our highly motivated and experienced team of nearly 2'700 employees are at service of our customers with uncompromising quality, proximity and agility. medmix is headquartered in Baar, Switzerland. Our shares are traded on the SIX Swiss Exchange (SIX: MEDX). We are looking for a Quality Technician to join us at medmix, at our new Greenfield Site outside of Atlanta, Georgia USA. This exciting opportunity will allow you use your skills to identify areas of improvement and propose recommendations to management. You will lead and drive the implementation of your recommendations and assess its impact to the business. If you are eager to learn, strive for personal development, are highly motivated and organized, and a great communicator, you can help us drive medmix to the next level. Job Description Job purpose Responsible for assisting with the implementation, management, and administration of the quality management system and ensuring products are manufactured per quality and regulatory requirements and industry best practices. Main Accountabilities and tasks May participate in “on the floor” audits of production personnel to ensure adherence to procedures and training effectiveness Conducts sampling, product testing, and visual inspection of components and/or finished goods; identifies nonconformances, if any, and ensures proper containment as required Completes accurate, timely, and legible documentation of all inspection/testing data Participates in weekly production walk-throughs to ensure quality compliance Engage in Safety, Quality, Production, and Plant related programs as required (Safety Observations, Meetings, Gembas, etc.) Participates in continuous improvement objectives to assure compliance with regulations Performs other duties as assigned by management Maintain and apply knowledge of current policies, regulations, and industrial processes for medmix USA Maintains quality records procedure and coordinates non-conformance reporting Compiles, analyze, and interprets statistical data related to quality operations May be required to cover position on their assigned shift due to absences for vacations, leave, etc. Perform all other miscellaneous duties as appropriately directed by Quality Management or designate Qualifications Desired experience and qualifications Work Experience: 1-3 years of experience in a regulated workplace preferred Education: Bachelor's degree preferred or equivalent with education and experience. Other: Experience with injection molding processes, parameters, and troubleshooting is preferred. 1-3 years of experience in a quality role preferred. Proficiency in personal computers, especially word processing software, spreadsheets, presentation, and database software. Ability to learn quickly and maintain the Quality Assurance metrics Knowledge of ISO standards or the ability to quickly learn and retain knowledge as required for system compliance Ability to perform work accurately and thoroughly and to work independently with minimal supervision Must be organized and can follow a systematic method of performing tasks and the ability to organize and direct a project to completion Must be self-directed and motivated to optimally utilize the available time to organize and complete expected work within given deadlines and reasonable work schedules Communication skills, both oral and written, as required to communicate effectively with others at all levels in the organization and to provide clear and concise reports and policies as needed. Ability to effectively present information publicly Ability to work well with subordinates, peers and superiors in all departments. Additional Information Benefits we offer: An innovative, vibrant and agile culture Growth opportunities in a globally successful and dynamic business on a growth trajectory Excellent employee benefits including Twelve (12) company paid holidays per year Medical, dental, vision, Life/AD&D, Short- and Long-Term Disability medmix Employee Savings Plan / 401k with 100% employer match up to 6% of your annual base salary Eligible to receive additional non-elective 401k contributions on a quarterly basis Employee Assistance Program Access to a wide range of discounts on shopping, entertainment and lifestyle Years of Service Awards medmix is an equal opportunity employer, committed to the strength of a diverse workforce. 93% of our employees would go above and beyond to deliver results - do you have the drive to succeed? Join us and boost your career, starting today!