Quality engineer jobs in Dothan, AL - 23 jobs

Allient Dothan is in growth mode and currently seeking a Senior Programmer / Manufacturing Engineer to join our team in Alabama! The Senior Programmer/Manufacturing Engineer position serves as the Subject Matter Expert/trainer/mentor/leader in support of the programming, operation and maintenance of all equipment within the Fabrication Center of Excellence. Responsibilities: Develop, optimize, and maintain CNC programs for multi-axis milling, turning, and mill-turn machines using CAD/CAM software (e.g., Mastercam, Siemens NX, or Fusion 360). Interpret complex engineering drawings, blueprints, and technical specifications to ensure accurate machining processes. Collaborate with engineering, production, and quality teams to improve manufacturability and reduce cycle times. Select appropriate cutting tools, speeds, and feeds to maximize efficiency and tool life. Conduct first article inspections and troubleshoot machining issues to ensure part conformance and quality standards. Lead continuous improvement initiatives in CNC programming, setup, and machining processes. Train and mentor junior programmers, engineers, operators, and machinists on best practices and new technologies. Lead workshops and one-on-one sessions on: CNC programming techniques Workholding and tooling strategies SMED (Single-Minute Exchange of Dies) Lean manufacturing principles Setup reduction and process standardization Maintain and update CNC program libraries and documentation in accordance with company standards. Support new product introductions (NPI) by developing prototype programs and refining processes. Ensure compliance with safety, quality, and regulatory requirements in all machining operations. Prepare geometric layout using computer-assisted drafting software to show location of reference points and direction of cutting paths Determine reference points and direction of machine cutting paths Analyze drawings, sketches, and design data of parts to determine dimension and configuration of cut, selection of cutting tools, and machine speeds and feed rates Prepare the CNC machine for production adjusts machine settings to the desired product specifications Complete quality control tests during the manufacturing stage and on the final product. Design and implement efficient workholding and tooling solutions for multi-axis machining. Collaborate with design and quality teams to ensure manufacturability and compliance with aerospace standards (AS9100, NADCAP, etc.). Champion Lean initiatives across the shop floor, focusing on waste reduction, cycle time improvement, and setup efficiency. Lead Kaizen events and support implementation of 5S, visual management, and standard work. Analyze machining processes to identify opportunities for cost savings and quality improvements. Minimum Qualifications: Bachelor's degree in Mechanical, Manufacturing, or Industrial Engineering (or equivalent experience). 8+ years of CNC programming experience with at least 3 years in aerospace or precision manufacturing. Deep knowledge of G-code, multi-axis machining (3-,4-, and 5-axis), blueprint reading, tight-tolerance aerospace components, and high-performance tooling. Proven track record of coaching and mentoring technical teams. Strong understanding of Lean, SMED, and continuous improvement methodologies. Excellent communication, leadership, and problem-solving skills and ability to lead root cause analysis and corrective actions. Familiarity with ERP/MES systems and digital manufacturing tools. Certifications in Lean Six Sigma or similar methodologies. Experience with aerospace quality standards (e.g., AS9100, NADCAP) Proficiency in CAD/CAM software such as Mastercam, Siemens NX, CATIA, or Fusion 360. Demonstrated experience with low-volume, high-mix production. Familiarity with aerospace materials and machining best practices for titanium, Inconel, and aluminum alloys. *To learn more about Allient, visit our website at *************** *Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Allient Inc. is currently seeking a Quality Engineer to join our team in Dothan, Alabama! The Quality Engineer position works directly with production and engineering to audit and analyze manufacturing processes and products for improvement using various methods of problem solving, testing and inspection. Responsible for all aspects of the Quality Management System of the site. Apply now! Responsibilities: * Develops, applies and maintains quality requirements and standards for development and manufacturing products by leading a "zero" defect culture across the organization through training, ongoing communication. * Designs and implements methods for process control, process improvement, testing and inspection. * Promotes and executes quality standards, inspection processes, test methodology, quality plans, documents and reports. * Provides timely and robust quality corrective and preventive solutions to reduce generation of scrap and rework as well as external quality failures. * Develops, executes and analyzes quality-reporting measures, COQ and COPQ both internal and external, identifies top opportunities, analysis, identify failures in need of prompt corrective action. * Participates in internal and external quality audits as well as serves as the principle advisor on all quality certifications including ISO, AS 9100, etc. * Monitors supplier quality performance and ensures incoming parts meet specified requirements. Works with suppliers on corrective actions. Minimum Qualifications: * Bachelor's degree in Engineering, preferably Mechanical or Electrical or equivalent work experience in lieu of a degree. * 0 - 8 years of work and/or intern/co-op experience in a technical, manufacturing environment * Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. * Solid computer skills include MS Office, engineering design software such as Solidworks, MatLab, Altium, etc Physical Demands: * The role is mostly office-based but may spend considerable time standing and walking on the production floor or development lab. * May be required to operate a computer as well as some production machinery and lab equipment. * Occasionally may have to lift and/or transport items weighing between 10 and 40 pounds. Work Environment: * Predominately office environment with occasional exposure to the production floor and development lab. * While on the production floor, employee may be subjected to moving mechanical parts and may be required to put on precautionary, protective wear such as safety glasses. * Some travel may be required. Don't let this opportunity pass you by - APPLY TODAY! To learn more about Allient Inc. visit *************** * Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Background Global Resources International, Inc. (GRI), a privately held US corporation, is a leading provider of value-added manufacturing services, medical and industrial products, and protective materials and solutions. GRI now offers an industry-leading portfolio of product development and material development services, and a broad range of vertically integrated manufacturing capabilities in support of our mission to provide the best value to our clients. Advanced Product Solutions (APS) is a wholly owned subsidiary of GRI. APS has a career-building opportunity for a Quality Engineer to join a dynamic and rapidly growing company. Job Summary The Quality Engineer will provide quality assurance support to the product development team, resolving bugs, defects, and other potential issues and ensuring that products meet customer specifications. Job Responsibilities Operate within Good Manufacturing Procedures (G.M.P) regulations and guidelines always in accordance with ISO13485. Comply with all Standard Operating Procedures (S.O.P's) Comply with the requirements of the Quality Management System and relevant standards Develops and initiates standards and methods for inspection, testing, and evaluation. Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data. Develops product specifications and sampling plans. Establishes program to evaluate precision and accuracy or production equipment and testing, measurement, and analytical equipment and facilities. Develops and implements methods and procedures for disposition and discrepant material and devises methods to assess cost and responsibility. Direct workers engaged in measuring and testing products and tabulating data concerning materials, product, or process quality and reliability. Reviews and approves validation protocols and final reports for equipment, product, and processes. Resolution and continuous improvement for root causes analysis, including NCE and Compliance. Investigates manufacturing and customer non-conformance's (complaints) through root cause analysis. Develops and implements corrective action necessary to resolve NCE/CAPA issues. Conducts effectively checks for all root cause analysis, CAPAs and document findings. Formulates responses to customer complaints. Facilitates improvement projects and teams. Interacts with customers and suppliers routinely to ensure that product quality is constantly maintained. Addresses all product quality issues for current products. Oversees and maintains all quality functions related to packaging and manufacturing. Participates in FDA inspections, ISO audits, and customer audits of the plant quality system. Performs supplier and internal audits. Other duties as assigned. Required Skills/Abilities Excellent verbal and written communication skills. Excellent organizational skills and attention to detail. Extensive knowledge of or the ability to quickly learn the organization's production processes. Excellent interpersonal skills with ability to serve as a liaison with developers, project managers, and customer support. Strong analytical and problem-solving skills. Proficient with Microsoft Office Suite or related software. Education and Experience B.S. in Engineering, Engineering Technology, Science is required. Or Minimum of 1-2 years Quality Engineering related experience and/or training is required. Six Sigma (Green Belt, Black Belt, etc.) or Process Excellence certification is preferred. Experience in an FDA regulated environment is preferred. Corrective / preventive action (CAPA): 1 year preferred Knowledge of regulations and industry applicable standards (ISO 13485, FDA CFR820, GMP, ISO11135). Knowledge of process improvement and other statistical process methods. Knowledge of process and product validations. Experience in healthcare industry and/or manufacturing industry is desired Physical Requirements Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 35 pounds at times. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Allient Inc. is currently seeking a Quality Engineer to join our team in Dothan, Alabama! The Quality Engineer position works directly with production and engineering to audit and analyze manufacturing processes and products for improvement using various methods of problem solving, testing and inspection. Responsible for all aspects of the Quality Management System of the site. Apply now! Responsibilities: Develops, applies and maintains quality requirements and standards for development and manufacturing products by leading a “zero” defect culture across the organization through training, ongoing communication. Designs and implements methods for process control, process improvement, testing and inspection. Promotes and executes quality standards, inspection processes, test methodology, quality plans, documents and reports. Provides timely and robust quality corrective and preventive solutions to reduce generation of scrap and rework as well as external quality failures. Develops, executes and analyzes quality-reporting measures, COQ and COPQ both internal and external, identifies top opportunities, analysis, identify failures in need of prompt corrective action. Participates in internal and external quality audits as well as serves as the principle advisor on all quality certifications including ISO, AS 9100, etc. Monitors supplier quality performance and ensures incoming parts meet specified requirements. Works with suppliers on corrective actions. Minimum Qualifications: Bachelor's degree in Engineering, preferably Mechanical or Electrical or equivalent work experience in lieu of a degree. 0 - 8 years of work and/or intern/co-op experience in a technical, manufacturing environment Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Solid computer skills include MS Office, engineering design software such as Solidworks, MatLab, Altium, etc Physical Demands: The role is mostly office-based but may spend considerable time standing and walking on the production floor or development lab. May be required to operate a computer as well as some production machinery and lab equipment. Occasionally may have to lift and/or transport items weighing between 10 and 40 pounds. Work Environment: Predominately office environment with occasional exposure to the production floor and development lab. While on the production floor, employee may be subjected to moving mechanical parts and may be required to put on precautionary, protective wear such as safety glasses. Some travel may be required. Don't let this opportunity pass you by - APPLY TODAY! To learn more about Allient Inc. visit *************** *Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Job Description The company is a $500M+, privately held company that is the largest plastics converter in the world and located 2 hours from the Gulf Coast. A highly automated plant, environmentally focused products, and employee centric operation, the company is financially stable and expanding. They have asked us to find a top-grade Process Engineer that can boost OEE, has experience with RJG and has automation experience for their operation in Southern Alabama. A qualified candidate will have: Three (3) plus years of experience as a Process Engineer in a plastics manufacturing environment Experience with RJG, automation and new tool start-up Experience processing using statistical process control to monitor, control and improve production processes Experience and track record of improving OEE metrics Track record of being self-motivated with the ability to hit the ground running

Requisition ID: 63269 Title: Engineer II QA - Manufacturing Division: Arthrex Manufacturing Inc (US02) Location: Ave Maria, FL Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for an Engineer II - QA for our manufacturing site in Ave Maria, FL. The ideal candidate will have a Bachelor's degree in Engineering and 2+ years experience in a Quality Control or Quality Assurance position in a Medical Device Company. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better. Essential Duties and Responsibilities: * Review design drawings for tolerance, inspect-ability and quality of design issues. * Work with suppliers to improve quality, and assist, where necessary, in supplier process validations. * Assist in the training of QC Inspectors on inspection techniques and the use of new equipment. * Participate in Internal and External quality audits as directed by the Quality Assurance Manager. * Support Risk Management by leading or participating in cross-functional team pFMEA's and Risk Assessments. * Support the AMI Engineering Change Management process by performing tasks as assigned. * Lead or Support the internal manufacturing First Article Inspection process, review First Article Inspection Reports and samples (internal and/or supplier). * Lead or Support equipment or process validation (IQ, OQ, PQ) * Lead or support Metrology with design and development of inspection methods and gages. * Create or review inspection method work instructions. * Lead or support Metrology with Measurement System Analysis (Gage R&R) studies. * Create Inspection Plans Supporting Receiving and In-Process Inspection. * Investigate complaints as requested by the Complaints/Reliability team. * Lead completion of Nonconformances (NCR's) as assigned: material disposition plans, evaluations, and action plans. * Perform routine Nonconformance and process trending and lead periodic Quality review meetings with the management team. * Lead or Support Continuous Improvement projects. * Lead or support the Environmental Monitoring program. * Complete Root Cause Analysis Investigations and define Corrective/Preventive Action Plans (CAPA's). * Perform Engineering Studies and Design of Experiments (DOE) as needed. Education and Experience: * Bachelor's degree in Engineering required. * 2 years experience in a Quality Control or Quality Assurance position in a Medical Device Company preferred. Knowledge and Skill Requirements/Specialized Courses and/or Training: * Technical knowledge in development methodologies including: Design Controls, GD&T, DOE, Process Verification and Validation. * SPC (Statistical Process Control) knowledge. * Working knowledge of process improvement tools (i.e.: Lean - PDCA, Six Sigma - DMAIC) and problem solving (i.e.: Kepner Tregoe, Lean A3, 5 Whys) preferred. * Working knowledge of risk assessments, PFMEAs, control plans, quality plans. * Strong communication skills and ability to communicate effectively with technical and non-technical staff. * Project management skills preferred. Machine, Tools, and/or Equipment Skills: Proficiency in the use of PC and programs, particularly Excel, Word (or equivalents if changed by the Company), mini Tab or similar statistical analysis software, SAP or similar inventory software, Agile or similar design lifecycle software, Pilgrim or similar QMS software. Knowledge of measurement and other inspection equipment. Manufacturing process knowledge Reasoning Ability: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. Mathematical Skills: Ability to comprehend and apply mathematical principles to the degree required to perform the job based upon job requirements. Prefer working knowledge and application of Statistics. Language and Communication Skills: Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures. 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 the 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 talk or hear. The employee is frequently required sit; use hands and fingers, to handle, or feel; and reach with hands and arms. The employee must occasionally lift and/or move up to 10 pounds. Vision Requirements: Visual acuity necessary to do the job safely and effectively. Specific vision abilities required by this job include close vision using a microscope and light source. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The area that this job is performed in is a general office or open cubicle/workstation environment. The noise level in the work environment is usually moderate. Arthrex Benefits * Medical, Dental and Vision Insurance * Company-Provided Life Insurance * Voluntary Life Insurance * Flexible Spending Account (FSA) * Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness) * Matching 401(k) Retirement Plan * Annual Bonus * Wellness Incentive Program * Free Onsite Medical Clinics * Free Onsite Lunch * Tuition Reimbursement Program * Trip of a Lifetime * Paid Parental Leave * Paid Time Off * Volunteer PTO * Employee Assistance Provider (EAP) All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law. Making People Better at Arthrex Lorem ipsum dolor sit amet consectetur. Cras fringilla elementum odio velit. Job Details Date: Dec 24, 2025 Requisition ID: 63269 Salary Range: Job title: Engineer II QA - Manufacturing Arthrex Location: Ave Maria, FL, US, 34142 Nearest Major Market: Naples Job Segment: QA Engineer, QA, Medical Device Engineer, Medical Device, Quality Assurance, Engineering, Quality, Healthcare, Technology

We are seeking a Quality Engineer who will assume a key role in the planning, development, implementation and maintaining of programs and procedures for the measurement of production quality, supplier quality, product returns, and environmental initiatives. This will include, but is not limited to, participating in the new product process, quality processes, vendor interaction, material dispositions, and working with the quality control group to ensure that new products and current products are ready for production. KEY RESPONSIBILITIES · New Product Quality Conformance · Supports quality in new product processes by serving as member and/or resource on development teams. · Writes, executes and reports test plans based upon scientific methods to support the new product process and on-going testing. · Ongoing Quality Conformance o Provides receiving-inspection technical support and writing/reviewing receiving-inspection procedures. · Leads the material review board (MRB) and implements corrective actions internally and externally with suppliers. · Supports and or provides input for published monthly performance reports as well as identify areas for improvement. · Support engineering solutions to quality assurance. · Plans, controls and ensures process and product quality in accordance with quality principles, which include planning processes, material control, acceptance sampling, and measurement systems. · FEMA (Failure Mode Effects Analysis) · Understand issues through progression. · Testing and supplier interaction. · Internal CAR if needed for understanding of diagnosed issue. · Lead FEMA projects. · Environmental · Provides support in our efforts to continually make products greener by supporting our Environmental initiatives. · Vendor/supplier interaction · Plans, conducts and report audits of suppliers. · Interfaces with suppliers concerning quality issues and represent the company interests. · Evaluates defective parts returned from the field. · Ensures compliance to all company quality policies. EDUCATION AND EXPERIENCE REQUIRED Education: Typically requires a bachelor's degree in business, math, science or equivalent. Experience: Typically requires 2 or more years of experience in quality engineering within a similar industry. KNOWLEDGE, SKILLS AND ABILITIES · Ability to influence decision-making and build critical relationships in a manufacturing organization. · Strong business and financial acumen and possesses a good working knowledge and understanding of business operations. · Demonstrated leadership skills and abilities. Ability to effectively manage a group of people across shifts and work under deadlines while maintaining positive employee relations. · Fundamental understanding of: quality philosophies, methods, tools, standards, organizational and team dynamics, customer expectations and satisfaction, supplier's relations and performance, interpersonal relationships, and professional ethics. · Understanding of quality systems and their development, documentation and implementation with respect to domestic and international standards or requirements. · Thorough understanding of problem-solving and quality improvement tools and techniques. This includes knowledge of management and planning tools, quality tools, preventative and corrective actions, and how to overcome barriers to quality improvements. · Ability to work across departmental lines within the organization. · Strong verbal and written communication skills to effectively develop and communicate quality policies, initiatives and problem solve · Ability to communicate effectively across departmental lines and externally as needed. · Proficient in MS Word, Excel spreadsheets and Power Point. · Ability to travel occasionally Qualifications EDUCATION AND EXPERIENCE REQUIRED Education: Typically requires a bachelor's degree in business, math, science or equivalent. Experience: Typically requires 2 or more years of experience in quality engineering within a similar industry. KNOWLEDGE, SKILLS AND ABILITIES · Ability to influence decision-making and build critical relationships in a manufacturing organization. · Strong business and financial acumen and possesses a good working knowledge and understanding of business operations. · Demonstrated leadership skills and abilities. Ability to effectively manage a group of people across shifts and work under deadlines while maintaining positive employee relations. · Fundamental understanding of: quality philosophies, methods, tools, standards, organizational and team dynamics, customer expectations and satisfaction, supplier's relations and performance, interpersonal relationships, and professional ethics. · Understanding of quality systems and their development, documentation and implementation with respect to domestic and international standards or requirements. · Thorough understanding of problem-solving and quality improvement tools and techniques. This includes knowledge of management and planning tools, quality tools, preventative and corrective actions, and how to overcome barriers to quality improvements. · Ability to work across departmental lines within the organization. · Strong verbal and written communication skills to effectively develop and communicate quality policies, initiatives and problem solve · Ability to communicate effectively across departmental lines and externally as needed. · Proficient in MS Word, Excel spreadsheets and Power Point. · Ability to travel occasionally Why is This a Great Opportunity We are seeking a Quality Engineer who will assume a key role in the planning, development, implementation and maintaining of programs and procedures for the measurement of production quality, supplier quality, product returns, and environmental initiatives. This will include, but is not limited to, participating in the new product process, quality processes, vendor interaction, material dispositions, and working with the quality control group to ensure that new products and current products are ready for production.

KEY RESPONSIBILITIES · New Product Quality Conformance o Supports quality in new product processes by serving as member and/or resource on development teams. o Writes, executes and reports test plans based upon scientific methods to support the new product process and on-going testing. · Ongoing Quality Conformance o Provides receiving-inspection technical support and writing/reviewing receiving-inspection procedures. o Leads the material review board (MRB) and implements corrective actions internally and externally with suppliers. o Supports and or provides input for published monthly performance reports as well as identify areas for improvement. o Support engineering solutions to quality assurance. o Plans, controls and ensures process and product quality in accordance with quality principles, which include planning processes, material control, acceptance sampling, and measurement systems. · FEMA (Failure Mode Effects Analysis) o Understand issues through progression. o Testing and supplier interaction. o Internal CAR if needed for understanding of diagnosed issue. o Lead FEMA projects. · Environmental o Provides support in our efforts to continually make products greener by supporting our Environmental initiatives. · Vendor/supplier interaction o Plans, conducts and report audits of suppliers. o Interfaces with suppliers concerning quality issues and represent Johnson Outdoors' interests. o Evaluates defective parts returned from the field. o Ensures compliance to all company quality policies. SUPERVISORY/MANAGEMENT RESPONSIBILITIES · None EDUCATION AND EXPERIENCE REQUIRED Education: Engineering Degree, Mechanical or Electrical Degree Experience: Typically requires 2 or more years of experience in quality engineering within a similar industry. KNOWLEDGE, SKILLS AND ABILITIES · Ability to influence decision-making and build critical relationships in a manufacturing organization. · Strong business and financial acumen and possess a good working knowledge and understanding of business operations. · Demonstrated leadership skills and abilities. Ability to effectively manage a group of people across shifts and work under deadlines while maintaining positive employee relations. · Fundamental understanding of: quality philosophies, methods, tools, standards, organizational and team dynamics, customer expectations and satisfaction, supplier's relations and performance, interpersonal relationships, and professional ethics. · Understanding of quality systems and their development, documentation and implementation with respect to domestic and international standards or requirements. · Thorough understanding of problem-solving and quality improvement tools and techniques. This includes knowledge of management and planning tools, quality tools, preventative and corrective actions, and how to overcome barriers to quality improvements. · Ability to work across departmental lines within the organization. · Strong verbal and written communication skills to effectively develop and communicate quality policies, initiatives and problem solve. Ability to communicate effectively across departmental lines and externally as needed. · Proficient in MS Word, Excel spreadsheets and Power Point. · Ability to travel (Amount of time required varies by location).

Allient Inc. is in growth mode and currently seeking a Process Engineer to join our team in Dothan, Alabama! The Process Engineer develops and sustains manufacturing processes to meet or exceed the technical requirements of our customers while achieving quality, throughput, and cost objectives. This individual will lead the implementation of manufacturing processes including, but not limited to process layout, equipment selection and installation, workflow, process flow, process characterization, process monitoring/control methods, material handling, tool selection, consumables, documentation, training and support. Apply now! Responsibilities: · Defines, characterizes and leads the implementation of new manufacturing processes. · Assures engineering & validation principals are applied to manufacturing process design and sustainability. · Develops manufacturing processes to be trouble free and ensure success every time targeting Zero Defects. · Supports concurrent engineering efforts by participating in design development projects representing manufacturing / quality assurance and the customer. · Designs, implements and documents procedures for manufacturing process control, process improvement, testing and inspection. · Establishes and implements reporting metrics for monitoring manufacturing process effectiveness and to enable managers to make sound product / process quality decisions. · Performs root-cause analysis and other problem-solving activities to identify corrective actions and process improvements utilizing Allied Systematic Tools (AST) and various quality tools including 3 Leg 5 Why. · Establishes collection and analysis systems of statistical data to predict trends that will affect improvement of product and process quality and capabilities targeting CpK 1.67 normal/CpK 2.0 KpC. · Analyzes customers' product specifications to establish efficient, cost-effective requirements for ease of manufacture and reproducible. · Assists with equipment selection and drive implementation of new equipment. · Performs necessary actions for process development and documentation to perform and achieve acceptable Customer PPAP/FAI submissions and approvals. · Develops, Monitors and improves manufacturing process performance and risk mitigation. · Participates in review process for customer purchase orders, contracts and change requests and ensure that the necessary criteria and provisions are included in manufacturing process and quality plans. · Interacts with customers to identify opportunities to improve quality and establish feedback with solution center and technical unit personnel. · Reports Key Performance Indicators (KPI's), quality issues, trends and losses to site management/value stream team/Regional Quality Manager. Minimum Qualifications: · Bachelor's degree in a discipline of engineering, · 2 - 8 years of related work experience necessary in a manufacturing environment · Working understanding of GMP, IS09000, and AS9100 required. · Experience in mechanical, process or product engineering and with automation of a manufacturing environment is preferred. · Excellent communication skills including presentations to external parties, internal leadership and facilitating training. Must be able to relate technical information to non-technical employees. Physical Demands: · Mostly office-based but may spend considerable time standing and walking on the production floor or development lab. · May be required to operate a computer as well as some production machinery and lab equipment. · Occasionally may have to lift and/or transport items weighing between 10 and 40 pounds. Work Environment: · Predominately office environment with occasional exposure to the production floor and development lab. · Will be subjected to moving mechanical parts and may be required to wear PPE such as safety glasses. · Some travel required. Don't let this opportunity pass you by - APPLY TODAY! To learn more about Allient Inc. visit *************** * Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Job Description Background Global Resources International, Inc. (GRI), a privately held US corporation, is a leading provider of value-added manufacturing services, medical and industrial products, and protective materials and solutions. GRI now offers an industry-leading portfolio of product development and material development services, and a broad range of vertically integrated manufacturing capabilities in support of our mission to provide the best value to our clients. Advanced Product Solutions (APS) is a wholly owned subsidiary of GRI. APS has a career-building opportunity for a Quality Engineer to join a dynamic and rapidly growing company. Job Summary The Quality Engineer will provide quality assurance support to the product development team, resolving bugs, defects, and other potential issues and ensuring that products meet customer specifications. Job Responsibilities Operate within Good Manufacturing Procedures (G.M.P) regulations and guidelines always in accordance with ISO13485. Comply with all Standard Operating Procedures (S.O.P's) Comply with the requirements of the Quality Management System and relevant standards Develops and initiates standards and methods for inspection, testing, and evaluation. Devises sampling procedures and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data. Develops product specifications and sampling plans. Establishes program to evaluate precision and accuracy or production equipment and testing, measurement, and analytical equipment and facilities. Develops and implements methods and procedures for disposition and discrepant material and devises methods to assess cost and responsibility. Direct workers engaged in measuring and testing products and tabulating data concerning materials, product, or process quality and reliability. Reviews and approves validation protocols and final reports for equipment, product, and processes. Resolution and continuous improvement for root causes analysis, including NCE and Compliance. Investigates manufacturing and customer non-conformance's (complaints) through root cause analysis. Develops and implements corrective action necessary to resolve NCE/CAPA issues. Conducts effectively checks for all root cause analysis, CAPAs and document findings. Formulates responses to customer complaints. Facilitates improvement projects and teams. Interacts with customers and suppliers routinely to ensure that product quality is constantly maintained. Addresses all product quality issues for current products. Oversees and maintains all quality functions related to packaging and manufacturing. Participates in FDA inspections, ISO audits, and customer audits of the plant quality system. Performs supplier and internal audits. Other duties as assigned. Required Skills/Abilities Excellent verbal and written communication skills. Excellent organizational skills and attention to detail. Extensive knowledge of or the ability to quickly learn the organization's production processes. Excellent interpersonal skills with ability to serve as a liaison with developers, project managers, and customer support. Strong analytical and problem-solving skills. Proficient with Microsoft Office Suite or related software. Education and Experience B.S. in Engineering, Engineering Technology, Science is required. Or Minimum of 1-2 years Quality Engineering related experience and/or training is required. Six Sigma (Green Belt, Black Belt, etc.) or Process Excellence certification is preferred. Experience in an FDA regulated environment is preferred. Corrective / preventive action (CAPA): 1 year preferred Knowledge of regulations and industry applicable standards (ISO 13485, FDA CFR820, GMP, ISO11135). Knowledge of process improvement and other statistical process methods. Knowledge of process and product validations. Experience in healthcare industry and/or manufacturing industry is desired Physical Requirements Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 35 pounds at times. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Allient Inc. is in growth mode and currently seeking a Process Engineer to join our team in Dothan, Alabama! The Process Engineer develops and sustains manufacturing processes to meet or exceed the technical requirements of our customers while achieving quality, throughput, and cost objectives. This individual will lead the implementation of manufacturing processes including, but not limited to: process layout,equipment selection and installation, workflow, process flow, process characterization, process monitoring/control methods, material handling, tool selection, consumables, documentation, training and support. Apply now! Responsibilities: · Defines, characterizes and leads the implementation of new manufacturing processes. · Assures engineering & validation principals are applied to manufacturing process design and sustainability. · Develops manufacturing processes to be trouble free and ensure success every time targeting Zero Defects. · Supports concurrent engineering efforts by participating in design development projects representing manufacturing / quality assurance and the customer. · Designs, implements and documents procedures for manufacturing process control, process improvement, testing and inspection. · Establishes and implements reporting metrics for monitoring manufacturing process effectiveness and to enable managers to make sound product / process quality decisions. · Performs root-cause analysis and other problem-solving activities to identify corrective actions and process improvements utilizing Allied Systematic Tools (AST) and various quality tools including 3 Leg 5 Why. · Establishes collection and analysis systems of statistical data to predict trends that will affect improvement of product and process quality and capabilities targeting CpK 1.67 normal/CpK 2.0 KpC. · Analyzes customers' product specifications to establish efficient, cost-effective requirements for ease of manufacture and reproducible. · Assists with equipment selection and drive implementation of new equipment. · Performs necessary actions for process development and documentation to perform and achieve acceptable Customer PPAP/FAI submissions and approvals. · Develops, Monitors and improves manufacturing process performance and risk mitigation. · Participates in review process for customer purchase orders, contracts and change requests and ensure that the necessary criteria and provisions are included in manufacturing process and quality plans. · Interacts with customers to identify opportunities to improve quality and establish feedback with solution center and technical unit personnel. · Reports Key Performance Indicators (KPI's), quality issues, trends and losses to site management/value stream team/Regional Quality Manager. Minimum Qualifications: · Bachelor's degree in a discipline of engineering, · 2 - 8 years of related work experience necessary in a manufacturing environment · Working understanding of GMP, IS09000, and AS9100 required. · Experience in mechanical, process or product engineering and with automation of a manufacturing environment is preferred. · Excellent communication skills including presentations to external parties, internal leadership and facilitating training. Must be able to relate technical information to non-technical employees. Physical Demands: · Mostly office-based but may spend considerable time standing and walking on the production floor or development lab. · May be required to operate a computer as well as some production machinery and lab equipment. · Occasionally may have to lift and/or transport items weighing between 10 and 40 pounds. Work Environment: · Predominately office environment with occasional exposure to the production floor and development lab. · Will be subjected to moving mechanical parts and may be required to wear PPE such as safety glasses. · Some travel required. Don't let this opportunity pass you by - APPLY TODAY! To learn more about Allient Inc. visit *************** *Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Allient Inc. is in growth mode and currently seeking a Process Engineer to join our team in Dothan, Alabama! The Process Engineer develops and sustains manufacturing processes to meet or exceed the technical requirements of our customers while achieving quality, throughput, and cost objectives. This individual will lead the implementation of manufacturing processes including, but not limited to: process layout,equipment selection and installation, workflow, process flow, process characterization, process monitoring/control methods, material handling, tool selection, consumables, documentation, training and support. Apply now! Responsibilities: · Defines, characterizes and leads the implementation of new manufacturing processes. · Assures engineering & validation principals are applied to manufacturing process design and sustainability. · Develops manufacturing processes to be trouble free and ensure success every time targeting Zero Defects. · Supports concurrent engineering efforts by participating in design development projects representing manufacturing / quality assurance and the customer. · Designs, implements and documents procedures for manufacturing process control, process improvement, testing and inspection. · Establishes and implements reporting metrics for monitoring manufacturing process effectiveness and to enable managers to make sound product / process quality decisions. · Performs root-cause analysis and other problem-solving activities to identify corrective actions and process improvements utilizing Allied Systematic Tools (AST) and various quality tools including 3 Leg 5 Why. · Establishes collection and analysis systems of statistical data to predict trends that will affect improvement of product and process quality and capabilities targeting CpK 1.67 normal/CpK 2.0 KpC. · Analyzes customers' product specifications to establish efficient, cost-effective requirements for ease of manufacture and reproducible. · Assists with equipment selection and drive implementation of new equipment. · Performs necessary actions for process development and documentation to perform and achieve acceptable Customer PPAP/FAI submissions and approvals. · Develops, Monitors and improves manufacturing process performance and risk mitigation. · Participates in review process for customer purchase orders, contracts and change requests and ensure that the necessary criteria and provisions are included in manufacturing process and quality plans. · Interacts with customers to identify opportunities to improve quality and establish feedback with solution center and technical unit personnel. · Reports Key Performance Indicators (KPI's), quality issues, trends and losses to site management/value stream team/Regional Quality Manager. Minimum Qualifications: · Bachelor's degree in a discipline of engineering, · 2 - 8 years of related work experience necessary in a manufacturing environment · Working understanding of GMP, IS09000, and AS9100 required. · Experience in mechanical, process or product engineering and with automation of a manufacturing environment is preferred. · Excellent communication skills including presentations to external parties, internal leadership and facilitating training. Must be able to relate technical information to non-technical employees. Physical Demands: · Mostly office-based but may spend considerable time standing and walking on the production floor or development lab. · May be required to operate a computer as well as some production machinery and lab equipment. · Occasionally may have to lift and/or transport items weighing between 10 and 40 pounds. Work Environment: · Predominately office environment with occasional exposure to the production floor and development lab. · Will be subjected to moving mechanical parts and may be required to wear PPE such as safety glasses. · Some travel required. Don't let this opportunity pass you by - APPLY TODAY! To learn more about Allient Inc. visit *************** *Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Requisition ID: 64046 Title: Engineer II - Molding Process Division: Arthrex Manufacturing Inc (US02) Location: Ave Maria, FL. Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex Manufacturing is currently seeking an Engineer II - Molding Process- to support the Engineering Manager with all support for the life cycle development of Class I, II and III medical devices, including new product development and maintenance of released products, in our Ave Maria, FL location. This includes design, develop, implement and improve manufacturing processes to produce cost effective quality medical device products and systems. Provide manufacturing engineering expertise to create, document and implement required procedures and documents. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better. Essential Duties and Responsibilities: * Work with project teams to identify issues and risks. During new product development integrate with Engineers, Design Engineers, Quality Engineers and the Packaging Department/and or Production Department to ensure cost effective new product development and introduction into manufacturing. * Develop a continuous improvement culture, skills sets and tools to enhance quality and operational excellence. * Lead/support process improvement initiative. * Introduce new equipment, products, and processes. Present process and equipment recommendations to Leadership Team with equipment reviews and plans for implementation. * Initiate new projects and be the Project Leader for key improvement initiatives, identifying best practices. * Develop an understanding of the current manufacturing processes and identify targets for improvement in operation efficiencies. * Develop manufacturing Work Instructions. * Provide process support on manufacturing technical issues. * Provide process and equipment expertise and support for daily clean-room sterile packaging efforts/and or production efforts. * Develop action plans to achieve short and long-range efficiency goals, selection of new production methods, designs of production fixtures, and methods to monitor efficiencies. * Lead and/or assist with implementation of packaging design/and or production specifications into manufacturing. * Monitor timelines and project deliverables to ensure adherence with approved project plans for manufacturing process development. * Develop protocols and coordinate validation of equipment and processes. * Stay current with methods used in the medical device industry to advance technologies. * Participate in defining Preventive Maintenance programs for clean room equipment/ and or production equipment associated with packaging or production activities. * Investigates and test in time reliability and quality improvements * Drives automation to replace the manual process as much as possible * Ensure Information and documentation is consistently accurate * Analyzes and plans workforce utilization, space requirements, and workflow, and designs layout of equipment and workspace for maximum efficiency. * Confers with vendors to determine product specifications and arrange for purchase of equipment, materials, or parts, and evaluates products according to specifications and quality standards. * Estimates production times, staffing requirements, and related costs to provide information for management decisions. * Applies statistical methods to estimate future manufacturing requirements and potential. * Provide process and equipment expertise and support. * Identify issues and risks to ensure cost effective new product development and introduction into manufacturing. Education and Experience: * Bachelor's degree in Engineering required. * 2 years of manufacturing process improvement experience required * Proven experience in leading process improvement projects. * Medical device manufacturing environment preferred. * Experience in workflow optimization, work measurement, efficiencies. * Recognized process improvement training (Lean, Six Sigma) preferred. Knowledge and Skill Requirements/Specialized Courses and/or Training: * Ability to work independently and effectively with cross functional teams. * Thorough understanding of manufacturing processes. * Detail oriented with strong analytical skills. * Strong communication skills and ability to communicate effectively with technical and non-technical staff. * Experienced user of MS Office Suite and CAD. * Experience with planning and conducting tests to validate equipment and processes. * Experience in completing technical documentation for engineering and manufacturing. * SPC (Statistical Process Control) knowledge. * Familiarity with clean room practices preferred. * Project management knowledge preferred. Machine, Tools, and/or Equipment Skills: Metal cutting equipment, finishing equipment, printing equipment, sealing equipment and custom fixturing. Language and Communication Skills: Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures. 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 the 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 talk or hear. The employee is frequently required sit; use hands and fingers, to handle, or feel; and reach with hands and arms. The employee must occasionally lift and/or move up to 10 pounds. To bend frequently and lift up to 30 lbs. on a regular basis. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing 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 occasionally exposed to moving mechanical parts, fumes or airborne particles, toxic or caustic chemicals, and risk of electrical shock. The noise level in the work environment is usually moderate. Arthrex Benefits * Medical, Dental and Vision Insurance * Company-Provided Life Insurance * Voluntary Life Insurance * Flexible Spending Account (FSA) * Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness) * Matching 401(k) Retirement Plan * Annual Bonus * Wellness Incentive Program * Free Onsite Medical Clinics * Free Onsite Lunch * Tuition Reimbursement Program * Trip of a Lifetime * Paid Parental Leave * Paid Time Off * Volunteer PTO * Employee Assistance Provider (EAP) All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law. Making People Better at Arthrex Lorem ipsum dolor sit amet consectetur. Cras fringilla elementum odio velit. Job Details Date: Dec 21, 2025 Requisition ID: 64046 Salary Range: Job title: Engineer II - Molding Process Arthrex Location: Ave Maria, FL, US, 34142 Nearest Major Market: Naples Job Segment: Process Engineer, Package Design, Medical Device, Medical Device Engineer, Orthopedic, Engineering, Manufacturing, Healthcare

KEY RESPONSIBILITIES * New Product Quality Conformance o Supports quality in new product processes by serving as member and/or resource on development teams. o Writes, executes and reports test plans based upon scientific methods to support the new product process and on-going testing. * Ongoing Quality Conformance o Provides receiving-inspection technical support and writing/reviewing receiving-inspection procedures. o Leads the material review board (MRB) and implements corrective actions internally and externally with suppliers. o Supports and or provides input for published monthly performance reports as well as identify areas for improvement. o Support engineering solutions to quality assurance. o Plans, controls and ensures process and product quality in accordance with quality principles, which include planning processes, material control, acceptance sampling, and measurement systems. * FEMA (Failure Mode Effects Analysis) o Understand issues through progression. o Testing and supplier interaction. o Internal CAR if needed for understanding of diagnosed issue. o Lead FEMA projects. * Environmental o Provides support in our efforts to continually make products greener by supporting our Environmental initiatives. * Vendor/supplier interaction o Plans, conducts and report audits of suppliers. o Interfaces with suppliers concerning quality issues and represent Johnson Outdoors' interests. o Evaluates defective parts returned from the field. o Ensures compliance to all company quality policies. SUPERVISORY/MANAGEMENT RESPONSIBILITIES * None EDUCATION AND EXPERIENCE REQUIRED Education: Engineering Degree, Mechanical or Electrical Degree Experience: Typically requires 2 or more years of experience in quality engineering within a similar industry. KNOWLEDGE, SKILLS AND ABILITIES * Ability to influence decision-making and build critical relationships in a manufacturing organization. * Strong business and financial acumen and possess a good working knowledge and understanding of business operations. * Demonstrated leadership skills and abilities. Ability to effectively manage a group of people across shifts and work under deadlines while maintaining positive employee relations. * Fundamental understanding of: quality philosophies, methods, tools, standards, organizational and team dynamics, customer expectations and satisfaction, supplier's relations and performance, interpersonal relationships, and professional ethics. * Understanding of quality systems and their development, documentation and implementation with respect to domestic and international standards or requirements. * Thorough understanding of problem-solving and quality improvement tools and techniques. This includes knowledge of management and planning tools, quality tools, preventative and corrective actions, and how to overcome barriers to quality improvements. * Ability to work across departmental lines within the organization. * Strong verbal and written communication skills to effectively develop and communicate quality policies, initiatives and problem solve. Ability to communicate effectively across departmental lines and externally as needed. * Proficient in MS Word, Excel spreadsheets and Power Point. * Ability to travel (Amount of time required varies by location).

Allient Inc. is in growth mode and currently seeking a Senior Programmer / Manufacturing Engineer to join our team in Dothan, Alabama! The Senior Programmer/Manufacturing Engineer position serves as the Subject Matter Expert/trainer/mentor/leader in support of the programming, operation and maintenance of all equipment within the Machine Center of Excellence. Apply now! Responsibilities: Develop, optimize, and maintain CNC programs for multi-axis milling, turning, and mill-turn machines using CAD/CAM software (e.g., Mastercam, Siemens NX, or Fusion 360). Interpret complex engineering drawings, blueprints, and technical specifications to ensure accurate machining processes. Collaborate with engineering, production, and quality teams to improve manufacturability and reduce cycle times. Select appropriate cutting tools, speeds, and feeds to maximize efficiency and tool life. Conduct first article inspections and troubleshoot machining issues to ensure part conformance and quality standards. Lead continuous improvement initiatives in CNC programming, setup, and machining processes. Train and mentor junior programmers, engineers, operators, and machinists on best practices and new technologies. Lead workshops and one-on-one sessions on: CNC programming techniques, Workholding and tooling strategies, SMED (Single-Minute Exchange of Dies), Lean manufacturing principles, Setup reduction and process standardization Maintain and update CNC program libraries and documentation in accordance with company standards. Support new product introductions (NPI) by developing prototype programs and refining processes. Ensure compliance with safety, quality, and regulatory requirements in all machining operations. Prepare geometric layout using computer-assisted drafting software to show location of reference points and direction of cutting paths Determine reference points and direction of machine cutting paths Analyze drawings, sketches, and design data of parts to determine dimension and configuration of cuts, selection of cutting tools, and machine speeds and feed rates Prepare the CNC machine for production adjusts machine settings to the desired product specifications. Complete quality control tests during the manufacturing stage and on the final product. Design and implement efficient workholding and tooling solutions for multi-axis machining. Collaborate with design and quality teams to ensure manufacturability and compliance with aerospace standards (AS9100, NADCAP, etc.). Champion Lean initiatives across the shop floor, focusing on waste reduction, cycle time improvement, and setup efficiency. Lead Kaizen events and support implementation of 5S, visual management, and standard work. Analyze machining processes to identify opportunities for cost savings and quality improvements. Minimum Qualifications: Bachelor's degree in Mechanical, Manufacturing, or Industrial Engineering (or equivalent experience). 8+ years of CNC programming experience with at least 3 years in aerospace or precision manufacturing. Deep knowledge of G-code, multi-axis machining (3-,4-, and 5-axis), blueprint reading, tight-tolerance aerospace components, and high-performance tooling. Proven track record of coaching and mentoring technical teams. Strong understanding of Lean, SMED, and continuous improvement methodologies. Excellent communication, leadership, and problem-solving skills and ability to lead root cause analysis and corrective actions. Familiarity with ERP/MES systems and digital manufacturing tools. Certifications in Lean Six Sigma or similar methodologies. Experience with aerospace quality standards (e.g., AS9100, NADCAP) Proficiency in CAD/CAM software such as Mastercam, Siemens NX, CATIA, or Fusion 360. Demonstrated experience with low-volume, high-mix production. Familiarity with aerospace materials and machining best practices for titanium, Inconel, and aluminum alloys. *To learn more about Allient, visit our website at *************** *Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Allient Inc. is in growth mode and currently seeking a Process Engineer to join our team in Dothan, Alabama! The Process Engineer develops and sustains manufacturing processes to meet or exceed the technical requirements of our customers while achieving quality, throughput, and cost objectives. This individual will lead the implementation of manufacturing processes including, but not limited to: process layout, equipment selection and installation, workflow, process flow, process characterization, process monitoring/control methods, material handling, tool selection, consumables, documentation, training and support. Apply now! Responsibilities: * Defines, characterizes and leads the implementation of new manufacturing processes. * Assures engineering & validation principals are applied to manufacturing process design and sustainability. * Develops manufacturing processes to be trouble free and ensure success every time targeting Zero Defects. * Supports concurrent engineering efforts by participating in design development projects representing manufacturing / quality assurance and the customer. * Designs, implements and documents procedures for manufacturing process control, process improvement, testing and inspection. * Establishes and implements reporting metrics for monitoring manufacturing process effectiveness and to enable managers to make sound product / process quality decisions. * Performs root-cause analysis and other problem-solving activities to identify corrective actions and process improvements utilizing Allied Systematic Tools (AST) and various quality tools including 3 Leg 5 Why. * Establishes collection and analysis systems of statistical data to predict trends that will affect improvement of product and process quality and capabilities targeting CpK 1.67 normal/CpK 2.0 KpC. * Analyzes customers' product specifications to establish efficient, cost-effective requirements for ease of manufacture and reproducible. * Assists with equipment selection and drive implementation of new equipment. * Performs necessary actions for process development and documentation to perform and achieve acceptable Customer PPAP/FAI submissions and approvals. * Develops, Monitors and improves manufacturing process performance and risk mitigation. * Participates in review process for customer purchase orders, contracts and change requests and ensure that the necessary criteria and provisions are included in manufacturing process and quality plans. * Interacts with customers to identify opportunities to improve quality and establish feedback with solution center and technical unit personnel. * Reports Key Performance Indicators (KPI's), quality issues, trends and losses to site management/value stream team/Regional Quality Manager. Minimum Qualifications: * Bachelor's degree in a discipline of engineering, * 2 - 8 years of related work experience necessary in a manufacturing environment * Working understanding of GMP, IS09000, and AS9100 required. * Experience in mechanical, process or product engineering and with automation of a manufacturing environment is preferred. * Excellent communication skills including presentations to external parties, internal leadership and facilitating training. Must be able to relate technical information to non-technical employees. Physical Demands: * Mostly office-based but may spend considerable time standing and walking on the production floor or development lab. * May be required to operate a computer as well as some production machinery and lab equipment. * Occasionally may have to lift and/or transport items weighing between 10 and 40 pounds. Work Environment: * Predominately office environment with occasional exposure to the production floor and development lab. * Will be subjected to moving mechanical parts and may be required to wear PPE such as safety glasses. * Some travel required. Don't let this opportunity pass you by - APPLY TODAY! To learn more about Allient Inc. visit *************** * Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Allient Inc. is in growth mode and currently seeking a Process Engineer to join our team in Dothan, Alabama! The Process Engineer develops and sustains manufacturing processes to meet or exceed the technical requirements of our customers while achieving quality, throughput, and cost objectives. This individual will lead the implementation of manufacturing processes including, but not limited to: process layout, equipment selection and installation, workflow, process flow, process characterization, process monitoring/control methods, material handling, tool selection, consumables, documentation, training and support. Apply now! Responsibilities: · Defines, characterizes and leads the implementation of new manufacturing processes. · Assures engineering & validation principals are applied to manufacturing process design and sustainability. · Develops manufacturing processes to be trouble free and ensure success every time targeting Zero Defects. · Supports concurrent engineering efforts by participating in design development projects representing manufacturing / quality assurance and the customer. · Designs, implements and documents procedures for manufacturing process control, process improvement, testing and inspection. · Establishes and implements reporting metrics for monitoring manufacturing process effectiveness and to enable managers to make sound product / process quality decisions. · Performs root-cause analysis and other problem-solving activities to identify corrective actions and process improvements utilizing Allied Systematic Tools (AST) and various quality tools including 3 Leg 5 Why. · Establishes collection and analysis systems of statistical data to predict trends that will affect improvement of product and process quality and capabilities targeting CpK 1.67 normal/CpK 2.0 KpC. · Analyzes customers' product specifications to establish efficient, cost-effective requirements for ease of manufacture and reproducible. · Assists with equipment selection and drive implementation of new equipment. · Performs necessary actions for process development and documentation to perform and achieve acceptable Customer PPAP/FAI submissions and approvals. · Develops, Monitors and improves manufacturing process performance and risk mitigation. · Participates in review process for customer purchase orders, contracts and change requests and ensure that the necessary criteria and provisions are included in manufacturing process and quality plans. · Interacts with customers to identify opportunities to improve quality and establish feedback with solution center and technical unit personnel. · Reports Key Performance Indicators (KPI's), quality issues, trends and losses to site management/value stream team/Regional Quality Manager. Minimum Qualifications: · Bachelor's degree in a discipline of engineering, · 2 - 8 years of related work experience necessary in a manufacturing environment · Working understanding of GMP, IS09000, and AS9100 required. · Experience in mechanical, process or product engineering and with automation of a manufacturing environment is preferred. · Excellent communication skills including presentations to external parties, internal leadership and facilitating training. Must be able to relate technical information to non-technical employees. Physical Demands: · Mostly office-based but may spend considerable time standing and walking on the production floor or development lab. · May be required to operate a computer as well as some production machinery and lab equipment. · Occasionally may have to lift and/or transport items weighing between 10 and 40 pounds. Work Environment: · Predominately office environment with occasional exposure to the production floor and development lab. · Will be subjected to moving mechanical parts and may be required to wear PPE such as safety glasses. · Some travel required. Don't let this opportunity pass you by - APPLY TODAY! To learn more about Allient Inc. visit *************** * Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Requisition ID: 64251 Title: Engineer SR I - Industrial Division: Arthrex Manufacturing Inc (US02) Location: Ave Maria, FL Arthrex is a global medical device company and a leader in new product development and medical education in orthopedics. An Engineer Sr I will work to increase the productivity of manufacturing and business-related processes while reducing waste by analyzing product specifications and then use mathematical models to design systems and methods that will help the business meet production goals. This position will be located in our manufacturing facility in Ave Maria Southwest Florida. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better. Essential Duties and Responsibilities: * Responsible to accurately develop/manage capacity models and analysis results for all shop floor and critical upstream supply activities * Integrate individual models with other factory processes and systems, support the efforts of other Manufacturing and Engineering teams to efficiently plan, forecast and execute the factory's capability to meet strategic goals/demands. * Work closely with Planning, Finance, Operations, and other stakeholders to develop, recommend, and /or execute capacity planning analysis * Create, maintain, and communicate capacity models, including management of key assumptions, simulation modeling, and proactively drive capacity solutions with and without capital investment. * Extract current status information from the current Manufacturing Execution Systems (QAD) and future (MES) systems for use in analysis of factory capacity and throughput, and to feed into additional simulation and statistical analysis tools. Collect and maintain capacity and production metrics. * Identify and develop reporting tools to provide performance and capacity related analysis insight and business awareness. Update, validate, and evaluate with the latest information to ensure accurate reporting. * Facilitate kaizen events targeting key improvements to drive productivity improvement meeting stated goals. * Develop, Implement, and Mentor a Lean Business Process (LBP) program to drive a culture of continuous improvement. * Develop and implement systems and improvement strategies for direct material flow (in plant transport, warehousing and assembly line supply, etc.) * Evaluate component mfg. process improvements and its impact to plant assembly operations (labor balancing, time studies, part presentation, error proofing, assembly methods, etc.) to minimize any negative impact to downstream processes. * Provide cost estimates to include Make/Buy decisions for rearrangements and engineering changes. * Coordinate equipment / process changes on assembly lines. * Evaluate and approve engineering changes prior to implementation on plant floor. * Develop an understanding of the current manufacturing processes and identify targets for improvement in transactional and operational efficiencies. * Identify issues and risks to ensure cost effective new product development and introduction into manufacturing. * May supervise other Engineering or manufacturing personnel. Education and Experience: * Bachelor's degree in Engineering. * 5 years of relevant experience required * Medical device manufacturing experience preferred. * Experience in workflow optimization, work measurement, and efficiencies. * Experience leading major cross-functional projects Knowledge and Skill Requirements/Specialized Courses and/or Training: * Recognized process improvement training (Lean, Six Sigma) preferred. * Demonstrated Strong Project Management skills * Strong desire to improve upon existing processes and drive efficiencies * Knowledge and experience in conducting time studies, mapping value streams * Ability to analyze data collected as well as other process inputs to recommend changes that lead to improvements * Ability to educate and motivate others and the ability to manage projects to a successful and timely completion. * Ability to identify, recommend, and implement continuous improvement within process, equipment or systems to increase throughput and meet financial goals * Ability to assist in financial planning and cost analysis by estimating production equipment costs * Ability to develop most efficient ways to use people, machines, materials, information, and energy * Ability to work independently and effectively with cross functional teams. * Thorough understanding of manufacturing processes. * SPC (Statistical Process Control) knowledge. * Strong communication skills and ability to communicate effectively with technical and non-technical staff. * Experienced user of MS Office Suite, CAD, and production simulation software. * Experience in completing technical documentation for engineering and manufacturing. * Familiarity with clean room practices preferred. * AutoCAD or Solidworks experience preferred Machine, Tools, and/or Equipment Skills: Metal cutting equipment, molding, EDM, grinding equipment, finishing equipment, printing equipment, sealing equipment and custom fixturing. Language and Communication Skills: Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing 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 occasionally exposed to moving mechanical parts, fumes or airborne particles, toxic or caustic chemicals, and risk of electrical shock. The noise level in the work environment is usually moderate Arthrex Benefits * Medical, Dental and Vision Insurance * Company-Provided Life Insurance * Voluntary Life Insurance * Flexible Spending Account (FSA) * Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness) * Matching 401(k) Retirement Plan * Annual Bonus * Wellness Incentive Program * Free Onsite Medical Clinics * Free Onsite Lunch * Tuition Reimbursement Program * Trip of a Lifetime * Paid Parental Leave * Paid Time Off * Volunteer PTO * Employee Assistance Provider (EAP) All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law. Making People Better at Arthrex Lorem ipsum dolor sit amet consectetur. Cras fringilla elementum odio velit. Job Details Date: Dec 31, 2025 Requisition ID: 64251 Salary Range: Job title: Engineer SR I - Industrial Arthrex Location: Ave Maria, FL, US, 34142 Nearest Major Market: Naples Job Segment: Facilities, Supply, Statistics, Orthopedic, Manufacturing Engineer, Operations, Data, Healthcare, Engineering

Allient Inc. is in growth mode and currently seeking a Senior Programmer / Manufacturing Engineer to join our team in Dothan, Alabama! The Senior Programmer/Manufacturing Engineer position serves as the Subject Matter Expert/trainer/mentor/leader in support of the programming, operation and maintenance of all equipment within the Machine Center of Excellence. Apply now! Responsibilities: Develop, optimize, and maintain CNC programs for multi-axis milling, turning, and mill-turn machines using CAD/CAM software (e.g., Mastercam, Siemens NX, or Fusion 360). Interpret complex engineering drawings, blueprints, and technical specifications to ensure accurate machining processes. Collaborate with engineering, production, and quality teams to improve manufacturability and reduce cycle times. Select appropriate cutting tools, speeds, and feeds to maximize efficiency and tool life. Conduct first article inspections and troubleshoot machining issues to ensure part conformance and quality standards. Lead continuous improvement initiatives in CNC programming, setup, and machining processes. Train and mentor junior programmers, engineers, operators, and machinists on best practices and new technologies. Lead workshops and one-on-one sessions on: CNC programming techniques Workholding and tooling strategies SMED (Single-Minute Exchange of Dies) Lean manufacturing principles Setup reduction and process standardization Maintain and update CNC program libraries and documentation in accordance with company standards. Support new product introductions (NPI) by developing prototype programs and refining processes. Ensure compliance with safety, quality, and regulatory requirements in all machining operations. Prepare geometric layout using computer-assisted drafting software to show location of reference points and direction of cutting paths Determine reference points and direction of machine cutting paths Analyze drawings, sketches, and design data of parts to determine dimension and configuration of cuts, selection of cutting tools, and machine speeds and feed rates Prepare the CNC machine for production adjusts machine settings to the desired product specifications. Complete quality control tests during the manufacturing stage and on the final product. Design and implement efficient workholding and tooling solutions for multi-axis machining. Collaborate with design and quality teams to ensure manufacturability and compliance with aerospace standards (AS9100, NADCAP, etc.). Champion Lean initiatives across the shop floor, focusing on waste reduction, cycle time improvement, and setup efficiency. Lead Kaizen events and support implementation of 5S, visual management, and standard work. Analyze machining processes to identify opportunities for cost savings and quality improvements. Minimum Qualifications: Bachelor's degree in Mechanical, Manufacturing, or Industrial Engineering (or equivalent experience). 8+ years of CNC programming experience with at least 3 years in aerospace or precision manufacturing. Deep knowledge of G-code, multi-axis machining (3-,4-, and 5-axis), blueprint reading, tight-tolerance aerospace components, and high-performance tooling. Proven track record of coaching and mentoring technical teams. Strong understanding of Lean, SMED, and continuous improvement methodologies. Excellent communication, leadership, and problem-solving skills and ability to lead root cause analysis and corrective actions. Familiarity with ERP/MES systems and digital manufacturing tools. Certifications in Lean Six Sigma or similar methodologies. Experience with aerospace quality standards (e.g., AS9100, NADCAP) Proficiency in CAD/CAM software such as Mastercam, Siemens NX, CATIA, or Fusion 360. Demonstrated experience with low-volume, high-mix production. Familiarity with aerospace materials and machining best practices for titanium, Inconel, and aluminum alloys. *To learn more about Allient, visit our website at *************** *Allient Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.