Quality engineer jobs in Johnson City, TN - 41 jobs

Our award-winning client is seeking a Quality Manager to join their team. Our award-winning global leader in high-performance battery separators seeks a passionate Quality Manager to join their team. Responsibilities: Spearhead IATF 16949 certification for our lithium-ion battery separator expansion project, ensuring the highest quality standards. Maintain company accreditations (ISO 9001, IATF 16949), guaranteeing compliance and exceeding industry benchmarks. Lead internal and customer quality audits to identify and address any potential issues. Champion continuous improvement by managing internal QMS audits and layered process audits. Develop and refine quality management system processes for optimal efficiency. Report key performance indicators (KPIs) to senior management, providing actionable insights. Foster a culture of quality awareness by effectively communicating customer requirements throughout the organization. Required Qualifications: A bachelor's degree in a relevant field is required. (e.g., Engineering, Quality Management). 5+ years of experience with IATF 16949 Quality Management Systems. Project management experience in the battery industry is a plus. IATF certification auditor certification preferred. Strong communication, collaboration, and customer service skills. Experience working across departments (Sales, R&D, Operations). Excellent written, verbal, and listening skills. Ability to work independently and manage multiple priorities.

Job Title: Quality Assurance Manager Work Location: OK/TN Department: Quality Reports To: Plant Manager Direct Reports: Quality Technicians / Inspectors FLSA: Exempt Wage Type: Annual Salary (DOE) The Quality Assurance Manager is responsible for overseeing the quality assurance and control functions within the HDPE manufacturing facility. This role ensures compliance with ISO, ASTM, AWWA, UL, and other applicable standards, while driving continuous improvement and operational excellence across all quality processes. The incumbent leads testing, inspection, and auditing programs to maintain the highest quality of materials and finished products. Key Responsibilities Quality Assurance & Compliance · Develop, implement, and maintain a Quality Management System (QMS) compliant with ISO 9001 and applicable regulatory standards. · Ensure all products meet customer, company, and industry specifications (ISO, ASTM, AWWA, FM, UL, etc.). · Conduct internal audits, support external audits, and coordinate certification renewals. · Manage product inspection, data collection, and disposition of on-hold materials. · Participate in customer and regulatory audits, addressing findings in a timely manner. · Review and update QA documentation (QTs, SQPs, L4 documents) and support periodic reviews. Inspection & Testing · Oversee incoming inspection of PE resin and additives to ensure conformity to specifications. · Supervise in-process and final product inspections (dimensional checks, hydrostatic pressure, tensile, and impact testing). · Analyze test data to identify trends and initiate corrective/preventive actions (CAPA). · Maintain calibration of gauges and testing instruments; manage gauge inventory and database accuracy. Process Control & Continuous Improvement · Partner with Production to monitor extrusion processes and critical control points. · Establish and maintain Standard Operating Procedures (SOPs) and work instructions. · Drive Lean and continuous improvement initiatives to reduce scrap, rework, and complaints. · Actively participate in 5S, BIQC, and preventive quality initiatives. Leadership & Training · Lead and develop the QA team to achieve department and plant objectives. · Deliver training on quality systems, defect identification, testing methods, and safety. · Promote a culture of accountability, learning, and teamwork within the plant. · Support Health & Safety initiatives and ensure adherence to PPE and safety standards. Customer & Supplier Relations · Manage customer complaints through structured root cause analysis and CAPA implementation. · Collaborate with suppliers to maintain material quality and support continuous improvement. · Provide technical support to customers on product performance and application. Qualifications · Minimum 5 years of QA/QC experience in HDPE or plastic manufacturing. · Strong understanding of HDPE extrusion, molding, and pipe testing methods. · Proficiency in quality tools (root cause analysis, CAPA, statistical analysis). · Knowledge of ISO, ASTM, UL, FM, and AWWA standards. · Experience with ERP systems and MS Office Suite. · Lean or Six Sigma certification preferred. · Strong leadership, communication, and problem-solving skills.

Quality Control Technician Full Job Description Tri-City Extrusion, Inc. is a leading manufacturer of Aluminum Extrusions for Commercial and Industrial Markets. We have an immediate opening for a Quality Control Technician. This is a great opportunity to work in our core business in our growing operation. The position duties include: Performing dimensional layouts and aesthetic inspections of prototype & production parts utilizing blue-prints and various gages. Performing Mechanical Properties testing to ensure metal integrity of extruded aluminum products. Facilitating calibration of test and measuring equipment. Performing process audits on a periodic basis. Successful candidate must be a self-starter with good math skills, basic computer skills (Microsoft Office), ability to demonstrate proficiency using various gages and blue prints with good attention to detail. High School diploma or equivalent required, prior experience in manufacturing quality required, ASQ certification a plus. Excellent benefits including medical, dental, vision, 401k and company paid life insurance. EEO Benefit Conditions: Waiting period may apply Only full-time employees eligible Benefits: Health insurance Dental insurance Vision insurance Paid time off This Company Describes Its Culture as: Outcome-oriented -- results-focused with strong performance culture Stable -- traditional, stable, strong processes People-oriented -- supportive and fairness-focused Team-oriented -- cooperative and collaborative Pay Frequency: Weekly Schedule: Monday to Friday Occasional weekends required Night shift Overtime Available This Job Is: A job for which military experienced candidates are encouraged to apply A job for which all ages, including older job seekers, are encouraged to apply Open to applicants who do not have a college diploma Job Type: Full-time Pay: From $19.58 to $23.75 per hour Benefits: 401(k) Dental insurance Health insurance Life insurance Paid time off Vision insurance Schedule: 8 hour shift Education: High school or equivalent (Preferred) Experience: Manufacturing: 1 year (Preferred) Quality control: 1 year (Preferred) Shift availability: Night Shift (Preferred) Day Shift (Preferred) Work Location: One location

Company / Location Information A.O. Smith is a global leader applying innovative technologies and energy-efficient solutions to products manufactured and marketed worldwide. The company is one of the world's leading manufacturers of residential and commercial water heating equipment and boilers, as well as a manufacturer of water treatment products for residential and light commercial applications. A. O. Smith is headquartered in Milwaukee, Wisconsin, with approximately 12,000 employees at operations in the United States, Canada, China, India, Mexico, the Netherlands, and the United Kingdom. Primary Function The Quality Engineering Early Career program offers individuals the opportunity to gain comprehensive experience and knowledge within A. O. Smith's quality engineering disciplines that support the business. The program spans approximately 15 - 18 months, providing hands-on experience through rotations in key quality functional areas. Each rotation lasts around 5 - 6 months, though the duration may vary based on the role and skills being developed. Participants will engage in a mentoring program with functional leaders and present their progress to the leadership team at the end of each rotation. Upon successful completion, participants will transition into a quality engineering role that aligns with their skills, career goals, and business needs. Growth & Development: The program is designed to equip candidates with the tools necessary to fast-track their career growth and become a valued member of A.O. Smith. Through extensive exposure to various quality engineering disciplines, participants will gain unique skills, understand the business, and build a broad network across the company to maximize their potential. Participants will also benefit from additional career development and support through the following opportunities: Mentor Program: The candidate will be partnered with a dedicated mentor that will provide coaching and guidance throughout the program. Professional Development: The candidate will benefit from various professional development opportunities, including: Presenting to business leadership at the end of rotations, highlighting completed projects, acquired skills, and key lessons learned Participating in formal classroom training on topics such as project management, presentation skills, quality management systems, quality engineering techniques, and more Gaining product / process knowledge and an understanding of product applications Responsibilities Performs routine quality engineering tasks using standard techniques under supervision. Provides entry level support to the senior engineer / supervisor. Performs a supervised role in ensuring that the company's and customers' requirements are met on assigned products, programs, areas, or functions. Develop competence in quality engineering methods by performing structured work assignments. Monitor and assist in the implementation of internal quality controls and testing to meet quality procedures and norms. Participate in Quality System assessments / audits (1st / 2nd / 3rd party) as assigned. Prepare quality analysis and provide input to recommend necessary changes to quality procedures. Participate in root cause analysis to determine the cause of quality problems and implement corrective and preventative actions under supervision. Perform any other activities as needed or as directed. Exemplify professional conduct in accordance with AOS Values Qualifications Minimum Qualifications: B.S. in Engineering or Engineering Technology (seeking upcoming / recent graduates): Mechanical Engineering, Industrial Engineering, Engineering Technology, and Mechatronics Engineering preferred. 0-2 years of applicable experience in or exposure to manufacturing, quality, and technical environments (would consider intern/co-op experience) Cumulative GPA of 3.0 or higher Strong communication and leadership abilities Must be open to relocation within the United States Travel may be required (up to ~40%) as necessary. Ability to work independently and as a team to meet deadlines and goals Preferred Qualifications: Prior internship / co-op experience in a manufacturing setting strongly preferred Exposure to blueprint interpretation and metrology methods are a plus Knowledge of statistical analysis methods a plus Exposure to Minitab (equivalent statistical analysis software) and Microsoft Office a plus We Offer Competitive compensation package and comprehensive benefits plans which include medical and dental insurance, company-sponsored life insurance, retirement security savings plan, short- and long-term disability programs and tuition assistance. #LI-Onsite #LI-AO ADA Statement & EEO Statement In developing this job description care was taken to include all competencies needed to successfully perform in this position. However, for Americans with Disabilities Act (ADA) purposes, the essential functions of the job may or may not have been described for purposes of ADA reasonable accommodation. All reasonable accommodation requests will be reviewed and evaluated on a case-by-case basis. We consider all applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, gender identity and expression, marital or military status. We also provide reasonable accommodations to qualified individuals with disabilities in accordance with the Americans with Disabilities Act and applicable state and local law.

Huf NA, Greeneville (TN) I United States (US) Junior Quality Engineer We are a leading developer and manufacturer of mechanical and electronic locking systems as well as car access and authorization systems for the global automotive industry. Founded in 1908 in Velbert, Germany, we are an independent, family-owned company with around 7,500 employees at locations in Europe, America and Asia and achieved sales of more than EUR 1.2 billion in the financial year 2023. Your Role * Perform inspections, basic data analysis, documentation, and response to nonconforming conditions * Read control plans, blue prints, and product specifications to determine product quality requirements * Full understanding of all quality requirements of the product and is responsible to maintain quality * Full understanding of work instructions related to appearance guidelines for painted parts to make decisions based on the guidelines * Communicate customer and internal concerns and follow up with quality alerts with the team * Responsible for safe launch activities including performing inspections, tests, and data analysis to detect defects and ensure products meet defined requirements * Perform visual inspection of painted product to identify cosmetic defects and color matching * Responsible for training metric for all associates along with maintaining the training records * Monitor all assembly and paint line and provide coaching to the associates on viewing and training * Analyze quality data and contribute to the continuous improvement of overall product quality Your Skills * High School Diploma/ General Education Degree (GED), Two year degree preferred * Excellent math and reading skills * Good Computer literacy (Microsoft Word, Excel, required; PowerPoint preferred) * Excellent attendance and work habits * Ability to work independently and make consistent decisions * Prior paint viewing experience preferred * Bilingual (Spanish) preferred but not mandatory * Experience with methods of 8D and 5 Whys What we offer * Full comprehensive health insurance, dental, vision, flexible spending account * Disability insurance * 401(k) with company match * Paid Time Off Huf celebrates diversity, supports inclusiveness and encourages individual expression in our workplace. We do not tolerate the harassment or discrimination toward any of our applicants or employees. We are an equal opportunity employer. Huf North America Automotive Parts Manufacturing, Corp. Michelle Myers

Apply now " Company: Dentsply Sirona, Inc Dentsply Sirona is the world's largest manufacturer of professional dental products and technologies, with a 130-year history of innovation and service to the dental industry and patients worldwide. Dentsply Sirona develops, manufactures, and markets a comprehensive solutions offering including dental and oral health products as well as other consumable medical devices under a strong portfolio of world class brands. Dentsply Sirona's products provide innovative, high-quality and effective solutions to advance patient care and deliver better and safer dentistry. Dentsply Sirona's global headquarters is located in Charlotte, North Carolina. The company's shares are listed in the United States on NASDAQ under the symbol XRAY. This position is located in Johnson City which is the largest city in the Tri-Cities area, located in the north eastern region of Tennessee at the foothills of the Appalachian Mountains. The city is a growing metropolis with invigorating music, enchanting culture, and exhilarating mountain adventures. Its natural beauty and fresh mountain air combined with amenities that are often only available in larger cities make Johnson City the perfect location. Bringing out the best in people As advanced as dentistry is today, we are dedicated to making it even better. Our people have a passion for innovation and are committed to applying it to improve dental care. We live and breathe high performance, working as one global team, bringing out the best in each other for the benefit of dental patients, and the professionals who serve them. If you want to grow and develop as a part of a team that is shaping an industry, then we're looking for the best to join us. Working at Dentsply Sirona you are able to: Develop faster - with our commitment to the best professional development. Perform better - as part of a high-performance, empowering culture. Shape an industry - with a market leader that continues to drive innovation. Make a difference -by helping improve oral health worldwide. Our Johnson City, TN Location is looking for someone to join our team as a Quality Engineer / Microbiological Specialist. We offer competitive wages and a full menu of benefits including health (3 options), dental (provided), vision, life (provided) + extra life, short-term and long-term disability (provided), 401k (retirement) with company matching, 10 holidays and paid time off. SCOPE The Quality Engineer / Microbiological Specialist is responsible for establishing, maintaining, and continuously improving all validation, sterilization, and microbiological control activities at the Johnson City site. This role serves as the site Subject Matter Expert (SME) for gamma sterilization, microbiological testing, environmental monitoring, and equipment and process validation across all manufacturing and support processes. The position ensures compliance with applicable standards and regulations (ISO 13485, ISO 11137, ISO 11737, and FDA 21 CFR 820), supports audit readiness, and drives risk-based improvements to maintain validated and controlled processes that ensure product quality and patient safety. KEY RESPONSIBILITIES * Sterilization Validation & Oversight * Lead and maintain sterilization validation programs for products sterilized by gamma radiation, ensuring full compliance with ISO 11137-1/-2/-3 and FDA 21 CFR 820.75. * Develop and execute sterilization validation protocols (IQ/OQ/PQ) and periodic requalification per the Dentsply Sirona global validation procedure. * Manage dose audit and bioburden monitoring programs, analyzing trends and escalating deviations through the QMS. * Support supplier qualification and change control related to contract sterilization facilities. * Collaborate with R&D and Manufacturing Engineering to ensure new or transferred products are compatible with established sterilization parameters. B. Microbiological Controls & Test Method Validation * Lead and maintain test method validations and verifications for microbiological assays (bioburden, sterility, bacterial endotoxins) in compliance with ISO 11737 parts 1, 2 and 3 and USP-NF 2024. * Oversee periodic method suitability testing and recovery studies with external laboratories. * Review and approve microbiological test reports, ensuring data integrity and traceability in SmartSolve. * Evaluate and approve laboratory control changes, ensuring continued suitability for intended use. C. Environmental & Cleanroom Monitoring * Own and maintain the environmental monitoring (EM) program for controlled areas and cleanrooms used for product assembly and packaging, ensuring compliance with ISO 14644 and ISO 14698. * Review EM trending data, initiate and lead investigations for out-of-limit (OOL) or alert-level events, and ensure CAPAs are properly documented in SmartSolve. * Support cleanroom qualification/requalification and pressure cascade verification activities in partnership with Facilities and Engineering. * Provide technical guidance to operations on aseptic practices, gowning, and material flow to prevent contamination. D. Compliance & Continuous Improvement * Ensure alignment with the Global Quality System (GQS) and local SOPs for sterilization, environmental control, and microbiological testing. * Author, review, and maintain SOPs, work instructions, and validation reports related to sterilization and microbiological processes. * Represent the site during internal and external audits (FDA, BSI, TÜV, MDSAP) as the sterilization and microbiology SME. * Identify opportunities for process improvements, risk reduction, and enhanced contamination control. E. Cross-Functional and Global Collaboration * Work closely with R&D, Manufacturing Engineering, Regulatory Affairs, and Supplier Quality to ensure robust microbiological control throughout the product lifecycle. * Support global DS projects involving sterilization or microbiological validation * Provide technical training and mentoring for manufacturing and quality teams on sterilization and microbiological principles. F. Equipment and process Validation * Serve as the site owner for equipment and process validation activities across all manufacturing and supporting processes, in alignment with ISO 13485:2016, 21 CFR 820.70 / 820.75, and Dentsply Sirona's Global Validation Policy. * Develop, execute, and maintain validation protocols (IQ/OQ/PQ) for production and laboratory equipment, utilities, and automated systems used in manufacturing, packaging, or testing. * Partner with Engineering and Manufacturing to ensure new or modified processes are validated before release for routine production. * Ensure validation master plans, schedules, and revalidation requirements are up to date and aligned with global QA standards. * Lead or support process characterization, risk assessments, and statistical capability studies (CpK, Ppk) during validation planning and execution. * Review and approve validation documentation prepared by other functions to ensure consistency, technical adequacy, and regulatory compliance. * Maintain validation traceability and control through SmartSolve or other designated QMS systems. * Act as the primary site interface for internal and external audits regarding validation programs, ensuring readiness and documentation integrity. * Provide technical guidance and training to engineers and production teams on validation principles, documentation, and lifecycle management. EDUCATION: Bachelor's or Master's degree in Microbiology, Biology, Biomedical/Quality Engineering, or a related discipline is preferred, or an equivalent combination of experience and education. CERTIFICATIONS/LICENSING * Six Sigma is preferred * American Society of Quality - Engineer preferred * Professional Engineering Certificate preferred Years and Type of Experience: 3-5+ years of experience in sterilization validation and microbiological quality systems in the medical device or pharmaceutical industry. Key Required Skills, Knowledge and Capabilities: * Strong knowledge of ISO 13485, ISO 11137, ISO 11737, ISO 14644, and FDA 21 CFR 820. * Experience with gamma sterilization validation and environmental control programs required. * Hands-on experience with SmartSolve, TrackWise, or equivalent electronic QMS preferred. * Strong analytical, documentation, and cross-functional communication skills. * Understanding of Good Manufacturing Practices, Quality Systems, Regulatory requirements, validation principles and manufacturing methods in Medical Device regulated environment. * Understanding of inputs, outputs, raw materials, waste, quality control, costs, and techniques for maximizing the manufacture and distribution of goods. * Creative problem solving, flexibility and sound negotiation skills. * Strong project management skills as well as an ability to multi-task. * Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry helpful. * Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. * Ability to analyze, estimate and evaluate data. * Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. * Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. * Ability to deal with a variety of abstract and concrete variables. * Ability to read, analyze and interpret common scientific and technical journals, financial reports and legal documents. * Ability to write reports, business correspondence and procedure manuals. * Ability to respond internally to common inquires or complaints from customers, regulatory agencies, or members of the business community. Ability to effectively present information to top management, groups and /or boards of directors. Dentsply Sirona is an Equal Opportunity/ Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or protected Veteran status. We appreciate your interest in Dentsply Sirona. If you need assistance with completing the online application due to a disability, please send an accommodation request to **************************. Please be sure to include "Accommodation Request" in the subject. For California Residents: We may collect the following categories of personal information in connection with the submission of your resume or application materials to us for employment, and if hired, your employment with us: identifiers (e.g., name, address, email address, birthdate); personal records (e.g., telephone number, signature, education information, criminal background information, passport number and visa information); consumer characteristics (e.g., sex, marital status, veteran status, race, disability, sexual orientation); professional or employment information (e.g., resume, cover letter, employment history, background check forms, references, certifications, transcripts and languages spoken); and inferences from personal information collected (e.g., a profile reflecting abilities and aptitudes). The above categories of personal information are collected for the following business purposes: performing recruitment and hiring services; processing interactions and transactions (e.g., to comply with federal and state laws requiring us to maintain certain records, managing the workforce); and security (e.g., detecting security incidents, protecting against fraudulent or illegal activity). For additional details and questions, contact us at **************************

Electro-Mechanical, LLC is seeking a Quality Technician to join our Federal Pacific division in Bristol, VA. In this role, you will perform critical in-process and final inspections on our padmount switchgear products, ensuring compliance with engineering specifications, safety standards, and customer requirements in a fast-paced manufacturing environment. This is an excellent opportunity for a detail-driven professional with strong inspection skills and a commitment to quality to make a meaningful impact on high-performance, American-made electrical equipment. Responsibilities: Conduct in-process and final inspections on padmount switchgear assemblies to verify electrical, mechanical, and dimensional conformance to drawings and specifications. Inspect fabricated components-including formed metal parts, welded structures, enclosures, and internal switchgear assemblies-for accuracy, finish, and structural integrity. Perform electrical checks such as continuity verification, grounding inspections, proper phasing, torque validation, and dielectric clearance assessments. Use precision measurement tools such as calipers, micrometers, tape measures, torque wrenches, and multimeters to validate product quality. Document inspection results, complete inspection reports, and issue nonconformance reports (NCRs) as needed. Work closely with Engineering, Production, and Quality teams to resolve issues, communicate defects, and support corrective action processes. Ensure switchgear components-including switches, bus bars, fuses, bushings, barriers, and cable compartments-meet all safety, functionality, and workmanship standards. Review blueprints, wiring diagrams, schematics, and work instructions to ensure accurate product build and inspection. Support continuous improvement initiatives focused on reducing rework, improving processes, and enhancing overall product reliability. Maintain compliance with ISO procedures and contribute to internal audit activities as assigned. Required Qualifications: Two-year technical degree in a related field or a minimum of two years of experience in manufacturing, inspection, quality assurance, or a related discipline. Strong ability to read and interpret mechanical drawings, wiring diagrams, and electrical schematics. Experience inspecting mechanical and/or electrical assemblies in an industrial environment. Familiarity with precision measurement tools and basic electrical testing equipment. Strong attention to detail and commitment to producing accurate, thorough inspection documentation. Effective communication skills with the ability to collaborate across Engineering, Production, and Quality teams. Solid problem-solving skills and a proactive mindset for identifying and addressing quality concerns. Working knowledge of ISO 9001 standards is a plus. Ability to work overtime or adjust schedules based on production needs. EMC expects that every team member will be guided by EMC's Guiding Principles. Disclaimer The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed PandoLogic. Category:Quality Control, Keywords:Quality Control / Quality Assurance Technician, Location:Bristol, VA-24201

The Rotating Equipment Reliability Engineer is responsible for developing and implementing reliability programs that enhance equipment performance, ensure employee safety, and safeguard environmental compliance. This role focuses on maximizing facility up-time, improving product quality, and driving cost efficiency. The Rotating Equipment Reliability Engineer reports directly to the Technical Engineering Manager. Key Responsibilities and Duties * Work with the Maintenance, Technical and Operations to establish, track, and achieve equipment reliability goals and objectives for the facility. * Participate in safety and environmental initiatives to ensure overall employee safety and regulatory compliance. * Develop and monitor predictive and preventative maintenance activities - oil analysis, vibration analysis, and infrared thermography. * Provide daily technical support to craftsmen, supervisors and other engineers to resolve equipment design, maintenance and operating issues for immediate and long-term solutions. * Assist in planning and execution of turnaround activities. * Provide technical input to determine priority and scope of equipment repairs. * Lead root cause failure investigations for mechanical related incidents. * Review engineering projects to ensure compliance with plant and corporate standards, and other applicable industry standards. * Assist in developing and maintaining plant mechanical engineering / safety standards. * Complete engineering design and documentation for small plant improvement and modification projects. * Develop and manage reliability projects for plant mechanical systems. * Review supplier data and witness shop tests. * Assume site On Call Manager responsibilities occasionally. * Other duties as assigned. Education and Experience * Bachelor's degree in Mechanical Engineering or other related field. * 5+ years of engineering experience preferably in a chemical manufacturing environment. * Project & budget management experience preferred. * This is a safety sensitive position which requires employees to disclose the use of any prescription medication that may affect his or her ability to safely perform the essential functions of this position. Skills and Knowledge * Understanding of compressor control systems. * Mechanics of turbines, axial compressors, reciprocating compressors, screw compressors, centrifugal pumps, positive displacement pumps and diaphragm pumps. * Working knowledge of Process Safety Management (PSM) and a good understanding of general process control. * Possesses strong organizational and communication skills. * Possesses complex problem solving, critical thinking, strong mathematics skills, systems evaluation, and operation analysis. * Experienced in RCFA, RCM, or equivalent methodology. * Competent computer knowledge - CMMS, Excel, Word, analysis software, etc. Work Environment US Nitrogen, LLC operates 24 hours a day, 365 days a year. This position will be exposed to all elements of the weather on the plant site. Austin Powder is an Equal Opportunity and Affirmative Action Employer and is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. Austin Powder also participates in E-Verify.

Job Description The Rotating Equipment Reliability Engineer is responsible for developing and implementing reliability programs that enhance equipment performance, ensure employee safety, and safeguard environmental compliance. This role focuses on maximizing facility up-time, improving product quality, and driving cost efficiency. The Rotating Equipment Reliability Engineer reports directly to the Technical Engineering Manager. Key Responsibilities and Duties Work with the Maintenance, Technical and Operations to establish, track, and achieve equipment reliability goals and objectives for the facility. Participate in safety and environmental initiatives to ensure overall employee safety and regulatory compliance. Develop and monitor predictive and preventative maintenance activities - oil analysis, vibration analysis, and infrared thermography. Provide daily technical support to craftsmen, supervisors and other engineers to resolve equipment design, maintenance and operating issues for immediate and long-term solutions. Assist in planning and execution of turnaround activities. Provide technical input to determine priority and scope of equipment repairs. Lead root cause failure investigations for mechanical related incidents. Review engineering projects to ensure compliance with plant and corporate standards, and other applicable industry standards. Assist in developing and maintaining plant mechanical engineering / safety standards. Complete engineering design and documentation for small plant improvement and modification projects. Develop and manage reliability projects for plant mechanical systems. Review supplier data and witness shop tests. Assume site On Call Manager responsibilities occasionally. Other duties as assigned. Education and Experience Bachelor's degree in Mechanical Engineering or other related field. 5+ years of engineering experience preferably in a chemical manufacturing environment. Project & budget management experience preferred. This is a safety sensitive position which requires employees to disclose the use of any prescription medication that may affect his or her ability to safely perform the essential functions of this position. Skills and Knowledge Understanding of compressor control systems. Mechanics of turbines, axial compressors, reciprocating compressors, screw compressors, centrifugal pumps, positive displacement pumps and diaphragm pumps. Working knowledge of Process Safety Management (PSM) and a good understanding of general process control. Possesses strong organizational and communication skills. Possesses complex problem solving, critical thinking, strong mathematics skills, systems evaluation, and operation analysis. Experienced in RCFA, RCM, or equivalent methodology. Competent computer knowledge - CMMS, Excel, Word, analysis software, etc. Work Environment US Nitrogen, LLC operates 24 hours a day, 365 days a year. This position will be exposed to all elements of the weather on the plant site. Austin Powder is an Equal Opportunity and Affirmative Action Employer and is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. Austin Powder also participates in E-Verify. Job Posted by ApplicantPro

The Rotating Equipment Reliability Engineer is responsible for developing and implementing reliability programs that enhance equipment performance, ensure employee safety, and safeguard environmental compliance. This role focuses on maximizing facility up-time, improving product quality, and driving cost efficiency. The Rotating Equipment Reliability Engineer reports directly to the Technical Engineering Manager. Key Responsibilities and Duties Work with the Maintenance, Technical and Operations to establish, track, and achieve equipment reliability goals and objectives for the facility. Participate in safety and environmental initiatives to ensure overall employee safety and regulatory compliance. Develop and monitor predictive and preventative maintenance activities - oil analysis, vibration analysis, and infrared thermography. Provide daily technical support to craftsmen, supervisors and other engineers to resolve equipment design, maintenance and operating issues for immediate and long-term solutions. Assist in planning and execution of turnaround activities. Provide technical input to determine priority and scope of equipment repairs. Lead root cause failure investigations for mechanical related incidents. Review engineering projects to ensure compliance with plant and corporate standards, and other applicable industry standards. Assist in developing and maintaining plant mechanical engineering / safety standards. Complete engineering design and documentation for small plant improvement and modification projects. Develop and manage reliability projects for plant mechanical systems. Review supplier data and witness shop tests. Assume site On Call Manager responsibilities occasionally. Other duties as assigned. Education and Experience Bachelor's degree in Mechanical Engineering or other related field. 5+ years of engineering experience preferably in a chemical manufacturing environment. Project & budget management experience preferred. This is a safety sensitive position which requires employees to disclose the use of any prescription medication that may affect his or her ability to safely perform the essential functions of this position. Skills and Knowledge Understanding of compressor control systems. Mechanics of turbines, axial compressors, reciprocating compressors, screw compressors, centrifugal pumps, positive displacement pumps and diaphragm pumps. Working knowledge of Process Safety Management (PSM) and a good understanding of general process control. Possesses strong organizational and communication skills. Possesses complex problem solving, critical thinking, strong mathematics skills, systems evaluation, and operation analysis. Experienced in RCFA, RCM, or equivalent methodology. Competent computer knowledge - CMMS, Excel, Word, analysis software, etc. Work Environment US Nitrogen, LLC operates 24 hours a day, 365 days a year. This position will be exposed to all elements of the weather on the plant site. Austin Powder is an Equal Opportunity and Affirmative Action Employer and is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. Austin Powder also participates in E-Verify.

ESSENTIAL JOB FUNCTIONS: Improve Uptime of the Coating Lines Diagnose Downtime and find solutions Understand the equipment needed for the Coating Lines Internal Equipment - cathodes, cooling tubs, magnetrons, etc. External Equipment - loaders/stackers, robots, power supplies, washers, conveyer systems, etc. Optimize Coater Configurations for current & future products Material Target Utilization Optimize Cleanout (Coater PM) Cycle Organization of people and equipment Design & implement data Collection and Analysis systems (e.g. coat zone usage) Time Study of Coating Line What are the current & future bottlenecks? Understand & analyze coating stack breakdowns Minimize process drift DOE for testing new coatings Support Maintenance and Engineering teams on current & future projects Work with the Coating Specialists and Process Control Technicians in the Control Booth to understand requirements for producing our Coatings Build charts and job aids to help them - understand equipment upgrades, provide insight based on historical data, etc. Work with QA to make sure process changes continue to improve efficiency while maintaining quality of our coatings Work with your team to diagnose and problem solve daily struggles out on the Coating Lines Design, fabricate, and test new tools and equipment for all departments Willing to work flexible hours to accommodate projects/production Some travel is required Must have good time management and organization skills - able to handle multiple projects at the same time Comfortable working safely on the production floor and working in a team environment Be self-motivated - continue analyzing the process and find ways to improve the system

Job Description Department: Manufacturing Engineering Job Title: Manufacturing Engineer Summary: This position is responsible for review of existing manufacturing processes and development of new manufacturing processes to support our production lines and ensure our ability to meet current manufacturing schedules and future growth targets. Essential Functions of the Job: The essential functions of this job require the person, with or without reasonable accommodations, to perform the following: Develop and improve new and existing production processes and methods for increasing output and efficiency, as well as reducing costs and preventing defects. Work to increase process stability to meet customer demand with minimum amount of resources. Lend technical expertise to the Sourcing Group for the review and selection of new suppliers for the localized production of any new component parts required when a production line is transferred. This includes: Identification of new potential suppliers Review of supplier capabilities Review of part requirements like tolerances and quality requirements Technical review of initial offers (primarily tooling concepts and designs) Develop process time standards, process flow, and layout for all new or transferred production lines Assist Production Supervisors in solving technical, tooling, quality, process, and maintenance problems affecting the daily operations in manufacturing. Participate in CIP (Continuous Improvement Process) and LEAN events as required for their individual areas of expertise. Assist the localization team regarding capital tooling and equipment. This may include externally purchased capital equipment, internally produced capital equipment, and inter-plant equipment transfers. Coordinate the updating of all production-related process documentation to reflect most current methods and requirements of assembly. Use of the following software programs when performing duties of this position: MRPII (MAC-PAC), CAD (SolidWorks, Pro Engineer or AutoCAD), MS Excel, MS Word, MS Powerpoint, several CAM software packages. MRPII-related (MacPac) activities this position monitors and controls: Process Routing (review and update of piece rates) Capacity Planning Work Center overhead cost review (annually) · Perform all other duties as assigned. Recommended Education and/or Experience Bachelors Degree in Engineering; or minimum five years related experience; or combination of education and related experience. Knowledge of LEAN principles (preferred) All Employees are expected to: · Follow the Employee Handbook policies and procedures and uphold organizational values. · Contribute to building a positive work environment. · Report for work consistently and on time. · Report to supervision conditions or practices that are unsafe to ebm-papst and its employees. Monday - Friday, 7:30 am to 4:00 pm

Job Description About Us At Tate we are passionate about everything we do. As an independent brand operating within Kingspan Group, a global plc group of companies, Tate has been recognized worldwide as an industry leader in the development and manufacture of data center infrastructure solutions and commercial office raised access floors, for over 60 years. With revenues of over $420m and growing, Tate plays a pivotal role in offering expertise in cutting edge design engineering in order to craft solutions, by working collaboratively with clients as a trusted partner. Tate continues to grow and expand, operating multiple manufacturing and commercial sites across the US, Europe, the Middle East, Asia, and Australia. We are excited about our fresh, dynamic, and inclusive team of experts working on new innovations and forward-thinking designs, as we remain a market leading player within our industry. We continue to invest heavily in the best available manufacturing tools and equipment needed to adhere to Tate's world class standards and in keeping with our Planet Passionate sustainability strategy, our focus is on having minimal climate impact. We are excited by potentially welcoming you as part of our team as we continue to grow on a worldwide scale. About the Role We are looking for a Quality Technician 1 to join our team. The Quality Technician 1 is responsible for quality inspection for all products to ensure they conform to all applicable company and quality standards. This position will test products after, in process, and in final stages to ensure quality levels are met. What You'll Do Ensures all test equipment is properly maintained and calibrated Performs routine & job specific load performance tests to ensure compliance with published specs. Performs incoming inspections on products received from vendor. Has a working knowledge of all equipment and machinery within the facility. Performs daily in process quality audits on products on production floor. Performs testing needed for qualifications of new or revised products. Maintains updated certified testing reports on standard products. Assists with continuous improvement of product and manufacturing processes to improve quality, reduce costs, and ensure product quality objectives are met. As assigned by supervisor, visits job sites to identify problems and recommends solutions. Maintains good housekeeping and follow established safety procedures. Performs other duties as assigned or directed by Team Leader/Supervisor. Follows all policies, procedures, and work instructions including Employee Handbook, Standard Operating Procedures (SOPs), Manufacturing Operating Procedures (MOPs), Job Safety Analysis (JSAs), and Safety Manual. Maintains awareness of individual contribution to and impact of the quality, safety, environmental, and product compliance policies and activities; reports all quality issues, unsafe acts, and unsafe conditions to the proper personnel. Additional Expectations Remain compliant with the Code of Conduct and Policies which includes the Kingspan Group Compliance Policy. Ensure that all duties related to product compliance are adhered to in accordance with the Product Compliance Policy, Laws, Regulations, and market demands. Responsible for all tasks to achieve compliance goals and demands of the Compliance Management System. Must raise concerns related to the Compliance Management System to their supervisor, manager, or any member of the Leadership Team, or through the confidential whistle blower service. What You'll Bring High school diploma or GED; or equivalent experience. Must be able to lift up to 50 lbs. unassisted. Must be able to stand, walk, bend, stoop or crouch for at least an 8-hour shift. Must be computer literate, including proficiency with Microsoft Office Products. Ability to use various tools and measuring instruments such as calipers, micrometers, tape measures, dial indicators, feeler gauges, etc. and verify all test equipment is in calibration and maintained in good working order. Strong shop-floor orientation. Knowledge of aluminum cutting and milling operation is a plus. Must be able to work in a fast-paced working environment with accuracy and integrity. Strong written and verbal communication skills. Detail-oriented. Three (3) plus years manufacturing experience. What You'll Get Pay range: $23 USD to $25 USD per hour. Career Scope and Advancement: As we grow, new positions and career opportunities arise, offering accelerated paths for the right candidates, locally and globally. World of Wellness Philosophy: We empower you to take charge of your health and well-being. You'll have access to a wide range of medical, dental, and vision benefits, along with personalized guidance from a “Health Advocate.” We also offer other supplemental options, including 401k, legal, disability, and theft insurance, to ensure your financial wellness. Corporate Social Responsibility: Through Planet Passionate we are determined to reduce our manufacturing carbon (CO2e) emissions to as close to zero as technically possible, together with halving carbon intensity in our primary supply chain. We are very involved in our community, and you will have ample opportunities to support us in creating a better world. Skills Development: Given the dynamic pace of our business and a strong collaborative environment, your new role will be diverse and multifaceted - allowing you to be more versatile and develop a broader skill set. Mentorship and development: At Tate, we don't believe in hierarchy, we work together as one team for one common goal. You will have access and exposure to our senior leaders and experts for learning in your role, and additionally mentorship for the future. Culture: We have a great team culture, highly collaborative, supportive, and social. Together we innovate, collaborate, take ownership, and strive for excellence. Stay connected with us on LinkedIn for insights into life at Tate. Join us in our mission to make a difference through exceptional solutions. Tate Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to legally protected characteristics. We are committed to providing reasonable accommodations to qualified individuals with disabilities. Employment may be contingent upon completion of post-offer requirements in accordance with applicable law.

Are you ready to see your future take flight? At GE Aerospace, we believe the world works better when it flies. We are a world-leading provider of jet engines, components, and integrated systems for commercial and military aircraft. We have a relentless dedication to the future of safe and more sustainable flight and believe in our talented people to make it happen. **Job Description** Job Summary Help invent the future of flight, lift people up, and bring them home safely as a GE Aerospace intern! The Manufacturing Engineering internship offers a distinct role based on your major and field of interest: **Manufacturing Engineering Internship:** In this role you will build a strong technical foundation in manufacturing and assembly processes. This may include key manufacturing, new product integration, new technology integration, continuous improvement, and cost out. This internship is a great first step for those interested in our MEDP or OMLP program after graduation. Essential Responsibilities Our Manufacturing and Supply Chain organizations combine passionate people, cutting-edge technology, and a culture of continuous improvement to provide the highest quality products to our customers. Members of our team are part of a fast-paced and dynamic environment. They typically have the benefit of getting hands-on experience with our products. In either internship experience, you'll be expected to: + Learn and understand state-of-the-art methods of manufacturing, + Support manufacturing and repair processes for component hardware and/or overall engine assembly, + Maintain high-quality standards via risk assessment, root cause analysis, corrective action, and the application of statistical controls + Ensure safe work conditions via Environmental, Health & Safety (EHS) initiatives + Learn and apply Lean and Six Sigma principles to drive productivity, on-time delivery, process capability, and stable operations in our increasingly complex and demanding environment + Supporting delivery efforts for sourced components by working with our shops and suppliers while building project management skills, negotiation skills, and business acumen Qualifications/Requirements: + Minimum 3.0 cumulative G.P.A. on a 4.0 scale without rounding + Attending a full-time registered and nationally accredited bachelor or graduate program (accepted majors are listed below) + Willingness and ability to work in any of the 35+ GE Aerospace U.S. locations + Reliable transportation, as many of our sites do not have public transportation available Degrees accepted: + Aeronautical/Aerospace Engineering + Ceramic Engineering + Chemical Engineering + Civil Engineering + Computer Engineering + Computer Science + Electrical Engineering / Electrical & Computer Engineering + Engineering Technology (various) + Fiber/Polymer Science + Industrial Engineering + Manufacturing Engineering + Materials Science/Engineering + Mechanical Engineering + Systems Engineering + Welding Engineering Or any relevant or similar major to the ones above Eligibility Requirements: Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. Desired characteristics: + Humble: respectful, receptive, agile, eager to learn + Transparent: shares critical information, speaks with honesty, contributes constructively + Focused: quick learner, strategically prioritizes work, committed, and takes initiative + Leadership ability: strong communicator, decision-maker, collaborative teamwork + Problem solver: analytical-minded, challenges existing processes, critical thinker + Comfortable working in a fast-paced shop floor environment around various machine tools and equipment + Preference will be given to those with prior internship, co-op or military experience in manufacturing/supply chain or engineering + Demonstrated commitment to community and/or university involvement Benefits: Pay rates for this position begin at $20/hour and increase for each undergraduate year completed. Relocation support and housing assistance is available for those who relocate to a new city. Equal Opportunity Employer: _GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is an_ Equal Opportunity Employer (******************************************************************************************************************************************************** _._ _Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law._ _This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3))._ **Additional Information** GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). **Relocation Assistance Provided:** Yes GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

The Sr. Quality Engineer, Validation provides technical and quality leadership in the planning, execution, and lifecycle management of validation programs primarily covering Facilities and Utilities and able to support site Quality improvement initiatives. They must be proficient with Equipment Qualifications, understand Computerized Systems Validation and be able to assess Process Validations in order to align tasks and risks used to support the Site Master Validation Plan (MVP). This role ensures that all validated and qualified systems supporting Pharmaceutical (Rx), OTC, and Cosmetic manufacturing operate in a state of control, and remain compliant with FDA 21 CFR Parts 210, 211, 820, and 11, EU Annex 15, ICH Q7-Q10, and GAMP 5 guidelines. The Sr. QE/Validation partners cross-functionally with Quality, Operations, Engineering, and Maintenance to manage validation and process qualification projects, strengthen process capability, enhance equipment reliability, and uphold Crown's Quality Systems through technical accuracy, risk-based validation, and data integrity excellence. Reporting to: Sr. Quality Assurance Manager, Technical Services (Validation) Location: Johnson City, TN - onsite Responsibilities/Essential Duties: Validation and Qualification Program Management: Support, write and/or execute Validation Master Plans (VMPs), User Requirement Specifications (URS), Design/Configuration Specifications (DS/CS), Installation/Operational/Performance Qualifications (IQ/OQ/PQ), and Validation Summary Reports (VSRs) in support of the Master Validation Plan. Lead Process Validation (PV) lifecycle activities, including Process Design, Process Qualification, and Continued Process Verification ensuring alignment with ICH Q8/Q9/Q10 and FDA PV Guidance (2011). Author and review Process Validation Protocols, define Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs), and apply statistical analysis to confirm process capability (Cpk/Ppk). Develop and maintain Requirements Traceability Matrices (RTMs) linking user requirements, risk assessments, and qualification test outcomes. Execute testing, verifications and assessments of risk for primarily Facilities and Utilities, including HVAC, USP Purified Water Systems, and Compressed Air. Coordinate area-related Equipment Qualification and Engineering Studies. Assist with establishing facility environmental controls such as Temperature Monitoring using Vaisala/ViewLinc. Possess skills for risk assessment evaluations, for example, area facility equipment including autoclaves, incubators, bulk processors, and packaging filling equipment. Ability to serve as the site's Facility and Utility Qualification expert, the Subject Matter Expert (SME) at a Senior level. Support Factory Acceptance Testing (FAT), Site Acceptant Testing (SAT), commissioning, and qualification transitioning for systems. Maintain validation deliverables in compliance with GDP and ALCOA+ data integrity principles. Process Validation and Lifecycle Management: Lead and execute Process Validation following FDA and ICH guidance, including process characterization, strategy development, and ongoing verifications. Partner with Manufacturing and QA to ensure validated processes consistently produce material meeting predetermined specifications and quality attributes. Perform data trending, statistical analysis, and process capability studies to monitor validated processes and identify opportunities for improvement. Support Continued Process Verification programs and control systems monitoring by maintaining control charts, analyzing deviations and trends, and providing periodic validation and qualification reviews. Ensure validation documentation completed is current, traceable, and readily available for inspection. Change Control and Procedural Controls: Author and support Change Controls, Engineering Studies, CAPAs, and Deviation Investigations associated with validation and process changes. Ability to access SOP instruction and controls. Identify and establish as needed any procedural and system controls to sustain validated and qualified states; document alarm limits and identify for assuring control over the process. Contribute to the development and maintenance of Validation SOPs, Work Instructions, and Templates to standardize validation activities. Cross-Functional Collaboration and Project Leadership: Coordinate communications among Quality, Operations, Engineering, and Maintenance to ensure timely execution of validation and process qualification projects. Provide technical validation guidance to project teams and ensure inspection readiness during internal, corporate, and regulatory audits. Lead validation-related meetings, track milestones, and communicate project progress to management and stakeholders. Process Improvement and Technical Expertise: Apply risk-based engineering principles and GAMP 5 methodologies to enhance process and equipment performance, reduce variability, and improve throughput. Lead root-cause investigations (5-Why, Fishbone, DMAIC), determine root cause or causes and implement Corrective and Preventive Action Plans (CAPAs) that truly strengthen process controls. Leverage historical data and validation archives to support continuous improvement and future technology transfer projects. Develop SME knowledge in all things Validation including cleaning validation and analytical method development and qualification to future support continued site knowledge and program continuity. Basic Qualifications: Bachelor's degree & 5+ years' directly related experience. Preferred Qualifications: Bachelor's degree in Engineering, Life Sciences, or related technical discipline. 5+ years' experience in Validation and Quality roles. Personnel and project supervisory experiences are preferred for the Senior Level role. Advanced degree and/or ASQ/ISPE certifications. Preferred 8 years' experience in Validation/Quality Roles with progressive experience in validation and/or process and/or Quality Engineer roles within a regulated cGMP environment. Proven experience writing and executing IQ/OQ/PQs, as well as writing Validation Plans, URS, RTM, and Summary Reports. Strong working knowledge of 21 CFR Parts 210, 211, 820, and 11, EU Annex 15, ICH Q8-Q10, and GAMP 5. Experience qualifying utilities, process equipment, and systems; familiarity with automation, PLC/HMI interfaces, and 21 CFR Part 11 data-integrity control. Expertise in authoring and executing validation protocols with scientific rationale, statistical justification, and clear acceptance criteria. Proficient in interpreting P&IDs, system flow diagrams, control logic, and engineering schematics. Skilled in using Microsoft Office suite and SharePoint. Advanced knowledge in QMS, LIMS, and automated Validation systems software. Experienced with firmware/hardware/software configuration management and system lifecycle documentation. Strong technical writing and analytical skills with ability to translate complex test data into concise regulatory documentation. Excellent written and verbal communication skills with diverse technical and operational audiences. Demonstrated ability to manage multiple concurrent validation and qualification projects. Strong analytical, organizational, and leadership capability, emphasizing accuracy, compliance, and cross-functional collaboration. Primarily office and controlled manufacturing floor environment; routine interaction with utility areas. Minimal lifting or physical exertion required. Occasional off-shift or weekend work during critical validation or qualification phases. Limited travel ( Company Summary: Revance is a fast-growing global aesthetics and skincare company focused on providing innovative aesthetics and market-leading skincare offerings throughout every stage of life. With a differentiated portfolio of products spanning 60 countries, Revance meets the evolving needs of patients and consumers worldwide through continued innovation and commercialization of new products and treatments. What Revance invests in you: Competitive Compensation including base salary and annual performance bonus. Flexible PTO, holidays, and parental leave. Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more! This section of the is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a “qualified individual with a disability” in all aspects of the employment relationship. A “qualified individual with a disability” is “an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job.” Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

The Maintenance Reliability Engineer is primarily responsible for continuing the development and implementation of the equipment reliability programs to ensure employee safety, provide environmental security, and maximize the facility's availability, product quality and cost effectiveness. The Maintenance Reliability Engineer will report directly to the Maintenance Manager. Key Responsibilities and Duties * Develop and maintain equipment overhaul/replacement intervals, oil analyses and change frequencies. * Standardize and optimize spare parts inventories. * Develop equipment breakdown, maintenance, and spare parts / back-up strategies. * Develop and implement equipment maintenance-improvement initiatives, such as reducing equipment repair durations and optimizing routine PM work. * Establish equipment PMs to be performed by operators. * Discuss equipment conditions with field operators daily to understand if they notice any changes in how the equipment is performing. * Track plant down times, their causes, and identify equipment "bad actors" and develop strategies for reducing plant outages. * Determine the root causes of breakdowns to develop PMs or suggest equipment changes to decrease the frequency or eliminate the breakdown issues. * Participate in safety and environmental initiatives to ensure overall employee safety and regulatory compliance. * Assist in planning and execution of turnaround activities. * Lead root cause failure investigations for equipment failure related incidents. * Assist in developing and maintaining plant mechanical engineering / safety standards. * Complete engineering design and documentation for small plant improvement and modification projects. * Develop and manage reliability projects for plant mechanical systems. * Other duties as assigned. Education and Experience * 18+ years of age * Bachelor's degree in Mechanical Engineering or other related field. * Chemical engineering experience in a manufacturing environment preferred. Skills and Knowledge * Familiar with TPM, RCM, Six Sigma, or other maintenance improvement concepts. * Possesses strong organizational and communication skills. * Possesses complex problem solving, critical thinking, strong mathematics skills, systems evaluation, and operation analysis. * Experienced in RCFA, RCM, or equivalent methodology. * Competent computer knowledge - CMMS, Excel, Word, analysis software, etc. Work Environment US Nitrogen, LLC operates 24 hours a day, 365 days a year. This position will be exposed to all elements of the weather on the plant site. This is a safety sensitive position which requires employees to disclose the use of any prescription medication that may affect his or her ability to safely perform the essential functions of this position. Austin Powder is an Equal Opportunity and Affirmative Action Employer and is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicant's race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. Austin Powder also participates in E-Verify.

Department: Manufacturing Engineering Job Title: Manufacturing Engineer Summary: This position is responsible for review of existing manufacturing processes and development of new manufacturing processes to support our production lines and ensure our ability to meet current manufacturing schedules and future growth targets. Essential Functions of the Job: The essential functions of this job require the person, with or without reasonable accommodations, to perform the following: * Develop and improve new and existing production processes and methods for increasing output and efficiency, as well as reducing costs and preventing defects. Work to increase process stability to meet customer demand with minimum amount of resources. * Lend technical expertise to the Sourcing Group for the review and selection of new suppliers for the localized production of any new component parts required when a production line is transferred. This includes: * Identification of new potential suppliers * Review of supplier capabilities * Review of part requirements like tolerances and quality requirements * Technical review of initial offers (primarily tooling concepts and designs) * Develop process time standards, process flow, and layout for all new or transferred production lines * Assist Production Supervisors in solving technical, tooling, quality, process, and maintenance problems affecting the daily operations in manufacturing. * Participate in CIP (Continuous Improvement Process) and LEAN events as required for their individual areas of expertise. * Assist the localization team regarding capital tooling and equipment. This may include externally purchased capital equipment, internally produced capital equipment, and inter-plant equipment transfers. * Coordinate the updating of all production-related process documentation to reflect most current methods and requirements of assembly. * Use of the following software programs when performing duties of this position: MRPII (MAC-PAC), CAD (SolidWorks, Pro Engineer or AutoCAD), MS Excel, MS Word, MS Powerpoint, several CAM software packages. * MRPII-related (MacPac) activities this position monitors and controls: * Process Routing (review and update of piece rates) * Capacity Planning * Work Center overhead cost review (annually) * Perform all other duties as assigned. Recommended Education and/or Experience * Bachelors Degree in Engineering; or minimum five years related experience; or combination of education and related experience. * Knowledge of LEAN principles (preferred) All Employees are expected to: * Follow the Employee Handbook policies and procedures and uphold organizational values. * Contribute to building a positive work environment. * Report for work consistently and on time. * Report to supervision conditions or practices that are unsafe to ebm-papst and its employees. Monday - Friday, 7:30 am to 4:00 pm

Job Description Job Title: Manufacturing Engineer Reporting to: Ragan Proffitt Company: Tate About Us At Tate, we are passionate about everything we do. As an independent brand operating within Kingspan Group, a global plc group of companies, Tate has been recognized worldwide as an industry leader in the development and manufacture of data center infrastructure solutions and commercial office raised access floors, for over 60 years. With revenues of over $420m and growing, Tate plays a pivotal role in offering expertise in cutting edge design engineering to craft solutions, by working collaboratively with clients as a trusted partner. Tate continues to grow and expand, operating multiple manufacturing and commercial sites across the US, Europe, the Middle East, Asia, and Australia. We are excited about our fresh, dynamic, and inclusive team of experts working on new innovations and forward-thinking designs, as we remain a market leading player within our industry. We continue to invest heavily in the best available manufacturing tools and equipment needed to adhere to Tate's world class standards and in keeping with our Planet Passionate sustainability strategy, our focus is on having minimal climate impact. We are excited to potentially welcome you as part of our team as we continue to grow on a worldwide scale. About the Role The Manufacturing Engineer will collaborate closely with Product Design Engineering, Project Management, and Manufacturing teams to support the complete product development and production lifecycle. The role requires the creation of detailed fabrication and assembly drawings, the development of manufacturing processes, and the implementation of process improvements to ensure high-quality and efficient production. This position demands a combination of technical engineering expertise and hands-on involvement in manufacturing operations and product testing. What You'll Do Produce part and assembly drawings, Bill of Materials (BOMs), and supporting documentation from CAD models to facilitate manufacturing, testing, and assembly. Design and modify manufacturing processes, including the development and adjustment of equipment for component fabrication, assembly, and installation. Support product sourcing, purchasing, and material selection in alignment with design requirements. Provide technical and engineering guidance to support day-to-day production operations and process improvement initiatives. Design and implement testing methods to validate system and product capabilities. Participate in technical reviews of requirements, specifications, and designs to ensure manufacturability and compliance with standards. Prepare detailed product reports by collecting, analyzing, and summarizing production and quality data. Additional Expectations Maintain awareness of individual contribution to quality, safety, environmental, and compliance standards. Report on all quality issues, unsafe acts, and unsafe conditions to the appropriate personnel immediately. Collaborate effectively across teams to ensure workflow efficiency and alignment with project timelines. Continuously identify opportunities to improve production efficiency, reduce waste, and enhance product quality. What You'll Bring Bachelor's degree in mechanical engineering or related discipline. Minimum of five years of experience in a manufacturing environment. Strong proficiency in CAD modeling, technical drawings, and machine design, with SolidWorks experience preferred. Comprehensive understanding of manufacturing processes and hands-on experience with automated manufacturing equipment. Experience with CAM software is considered an advantage. Strong analytical and problem-solving skills, with the ability to design processes and troubleshoot manufacturing challenges. Commitment to quality, safety, compliance, and continuous improvement. What You'll Get Pay range: $70,000 USD to $85,000 USD. This role is eligible for a discretionary bonus. Career Scope and Advancement: As we grow, new positions and career opportunities arise, offering accelerated paths for the right candidates, locally and globally. World of Wellness Philosophy: We empower you to take charge of your health and well-being. You'll have access to a wide range of medical, dental, and vision benefits, along with personalized guidance from a “Health Advocate.” We also offer other supplemental options, including 401k, legal, disability, and theft insurance, to ensure your financial wellness. Corporate Social Responsibility: Through Planet Passionate we are determined to reduce our manufacturing carbon (CO2e) emissions to as close to zero as technically possible, together with halving carbon intensity in our primary supply chain. We are very involved in our community, and you will have ample opportunities to support us in creating a better world. Skills Development: Given the dynamic pace of our business and a strong collaborative environment, your new role will be diverse and multifaceted - allowing you to be more versatile and develop a broader skill set. Mentorship and development: At Tate, we don't believe in hierarchy; we work together as one team for one common goal. You will have access and exposure to our senior leaders and experts for learning in your role, and additional mentorship for the future. Culture: We have a great team of culture, highly collaborative, supportive, and social skills. Together we innovate, collaborate, take ownership, and strive for excellence. Stay connected with us on LinkedIn for insights into life at Tate. Join us in our mission to make a difference through exceptional solutions. Tate Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to legally protected characteristics. We are committed to providing reasonable accommodations to qualified individuals with disabilities. Employment may be contingent upon completion of post-offer requirements in accordance with applicable law. #IND123 #ZR

Are you ready to see your future take flight? At GE Aerospace, we believe the world works better when it flies. We are a world-leading provider of jet engines, components, and integrated systems for commercial and military aircraft. We have a relentless dedication to the future of safe and more sustainable flight and believe in our talented people to make it happen. Job Description Job Summary Help invent the future of flight, lift people up, and bring them home safely as a GE Aerospace intern! The Manufacturing Engineering internship offers a distinct role based on your major and field of interest: Manufacturing Engineering Internship: In this role you will build a strong technical foundation in manufacturing and assembly processes. This may include key manufacturing, new product integration, new technology integration, continuous improvement, and cost out. This internship is a great first step for those interested in our MEDP or OMLP program after graduation. Essential Responsibilities Our Manufacturing and Supply Chain organizations combine passionate people, cutting-edge technology, and a culture of continuous improvement to provide the highest quality products to our customers. Members of our team are part of a fast-paced and dynamic environment. They typically have the benefit of getting hands-on experience with our products. In either internship experience, you'll be expected to: * Learn and understand state-of-the-art methods of manufacturing, * Support manufacturing and repair processes for component hardware and/or overall engine assembly, * Maintain high-quality standards via risk assessment, root cause analysis, corrective action, and the application of statistical controls * Ensure safe work conditions via Environmental, Health & Safety (EHS) initiatives * Learn and apply Lean and Six Sigma principles to drive productivity, on-time delivery, process capability, and stable operations in our increasingly complex and demanding environment * Supporting delivery efforts for sourced components by working with our shops and suppliers while building project management skills, negotiation skills, and business acumen Qualifications/Requirements: * Minimum 3.0 cumulative G.P.A. on a 4.0 scale without rounding * Attending a full-time registered and nationally accredited bachelor or graduate program (accepted majors are listed below) * Willingness and ability to work in any of the 35+ GE Aerospace U.S. locations * Reliable transportation, as many of our sites do not have public transportation available Degrees accepted: * Aeronautical/Aerospace Engineering * Ceramic Engineering * Chemical Engineering * Civil Engineering * Computer Engineering * Computer Science * Electrical Engineering / Electrical & Computer Engineering * Engineering Technology (various) * Fiber/Polymer Science * Industrial Engineering * Manufacturing Engineering * Materials Science/Engineering * Mechanical Engineering * Systems Engineering * Welding Engineering Or any relevant or similar major to the ones above Eligibility Requirements: Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. Desired characteristics: * Humble: respectful, receptive, agile, eager to learn * Transparent: shares critical information, speaks with honesty, contributes constructively * Focused: quick learner, strategically prioritizes work, committed, and takes initiative * Leadership ability: strong communicator, decision-maker, collaborative teamwork * Problem solver: analytical-minded, challenges existing processes, critical thinker * Comfortable working in a fast-paced shop floor environment around various machine tools and equipment * Preference will be given to those with prior internship, co-op or military experience in manufacturing/supply chain or engineering * Demonstrated commitment to community and/or university involvement Benefits: Pay rates for this position begin at $20/hour and increase for each undergraduate year completed. Relocation support and housing assistance is available for those who relocate to a new city. Equal Opportunity Employer: GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3)). Additional Information GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). Relocation Assistance Provided: Yes