services. Essential Responsibilities: Lead the department through communication of company and department goals, setting clear expectations and active coaching/development of others. Ensure Source Inspection process effectively reduces risk and minimizes cost due to fabrication errors.
Promote resolution of Quality issues with Suppliers while monitoring all quality issues to ensure systematic problems are addressed. Develop new Quality requirements to meet N/E goals. Development of customer relationships both at the project level and management level. Proactively work with department heads to create a high-performance team. Be involved in industry organizations that provide support to
our quality efforts and provide an avenue for input into quality requirement changes. Qualifications: To perform this job satisfactorily, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill and/or ability, and environmental conditions required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Knowledgeable about heavy fabrication, welding, NDE, inspection. Knowledge of ASME and AWS specifications. Good communication skills, both verbal and written. Excellent people skills. Good analytical thinking ability and problem resolution
skills. Four-year college education, engineering discipline preferred.
5 8 years experience in the quality field (ASME or similar code experience). Management/Supervisory experience preferred. Travel up to 20% by car or plane. Lift or carry 11 20 lbs. Ability to read, write, problem solve, make quick decisions, interpret data and analyze results; effective written and verbal communication is essential. Required Knowledge, Skills, and Abilities: (Companies ATS Questions) : 1. Do you have 5 8 years experience in the quality field? Please explain. 2. Do you have experience with ASME or similar code experience and AWS specifications? Please explain. 3. Do you have a Four-year college degree (engineering discipline preferred)?
Please explain. 4. Do you have Management/Supervisory experience? Please explain.5. Do you have knowledge about heavy fabrication, welding, NDE, inspection? Please explain. 6. Describe your experience with or participated in ISO program and audits. Please elaborate 7. Describe your experience with ASME Section 1 Code, NDE methods, basic welding, etc. Please elaborate 8. Describe your ability to manage a quality assurance manual/program as well as their experience with ASME audits. Please elaborate 9. Must be a US Citizen or Green Card holder.
in focused on the future? If you are interested, keep reading! Electrical Component Tester start at $19.00/hour with higher offers to those with experience. We offer great benefits with 10 paid holidays, paid time off that starts to accrue on your first day, company paid basic life insurance and long-term disability, access to medical/dental/vision/other insurance, 401(k) with a company match, and comfortable, safe environment.
Who is Bitrode Corporation? With customers around the world and the United States, Bitrode is a manufacturing company for Cell, Module, and Pack Battery Testing Equipment. We offer an extensive product line of battery formation and laboratory test equipment, as
well as software tools, battery simulation and manufacturing automation tools appropriate to all battery applications and chemistries. If you are unsure what some of these are, just remember with electric vehicles and battery power as a goal for the future, we matter in that future.
We have a set of core values that start with safety, customer focus, and end with cooperation. We have managers, supervisors, and leads that work to listen to our employees and train them on what they do not know about our products. We strive to work as a team to get our products built, tested, and shipped to our customers. Our CEO knows every employee and takes time to personally welcome each individual to
our organization. What do our Electrical Component Testers Do? Our Electrical Component Testers put our products through specific electrical testing.
You would be presented testing requirements and an assembled machine. You would need to properly connect the machine to high power electricity, with all safety precautions in place. Then, you would test the machine using Bitrode created software meant to run the machine. You would use multi-meters, High Potential test equipment, digital oscilloscope, PC based monitoring, and variable transformers. You would be responsible to record all testing data and even write reports on the computer. We must know in writing that our products are working properly for our customers before they ever leave the building.
If testing shows that there is a problem with the machine, you will need to troubleshoot the machine, resolve the issue, fix the problem, and retest the machine. Throughout the troubleshooting process, you will work anywhere from testing PCBs on a benchtop to analyzing power electronics used in our units. You will need to be able to roll-up your sleeves and do wiring and work with hand tools to rework products. You would need to be comfortable testing products at power levels up to 600VAC 3-phase and 2000VDC.
We will provide you with arc flash protective clothing for your safety. We also have a reimbursement program for prescription safety glasses and toe protective shoes. You will be given work assignments so that you know what to work on. You will focus on testing our products correctly, the first time. If you need to clarify something, we have a lead working near you so you can just ask. Managers are out on the production floor to resolve any issues that arise. Once you are fully trained, you may be asked to travel to customer sites to service or commission our machines. This requires you to be a self-starter.
You would need to make scheduled flights and drive to various locations in the USA on your own. You would need to professionally represent Bitrode while at the customer. What makes you qualified for this role? You need to: Have knowledge of electrical equivalent to a 2-year degree in Electrical Engineering. Be able to read schematics and have knowledge of electrical/electronic circuitry. Be comfortable with power electronics, i. e. not only cabinet and module level testing but board level as well. Have proficient computer skills Be dependable and reliable to show up to work and do your job.
Please be able to pay attention to details. Be willing and able to learn our products for testing purposes. Have or be able to obtain a driver's license, if/when asked to travel. Any experience in electrical product testing would be amazing!
and cost saving for existing products. This role offers the opportunity to work with customers, sales, manufacturing, purchasing and quality departments. Essential Job Duties: Reviews, maintains, and updates the Quality Assurance Manual and other Quality department procedures.
Prepares, plans, and leads on behalf of the organization, all external audits both regulatory and customer audits (ISO 13485, FDA, and MDR) related to the products manufactured onsite. Leads, plans, and implements corrective actions, internal audits to ensure the highest product quality and continuous improvement. Supervises and directs the actions of a Quality Engineering Technician and receiving inspector. Works
in collaboration with design and manufacturing engineering to implement new products, design changes and to ensure all products and processes meet customer and regulatory specifications.
Works cross functionally with all departments to ensure that the organization is aligned with the company's quality policies and meets all regulatory and customer requirements. Maintains all records regarding quality documentation, calibration, and corrective actions. Leads and drives till resolution all customer complaints and corrective actions. Maintains and updates customer complaint documentation. Leads team to perform and documentation of FAIs. The technical lead on incoming and in process inspection
equipment selection and calibration requirements. Works with the Director of Quality and Operations to drive total product quality and a spirit of continuous improvement.
Required Education: Bachelor's degree or equivalent experience. Required Experience/Skills: Knowledge of Quality Control Systems. Experience in high pressure flow control valves a plus. Experience with Microsoft Excel, Word, and Power Point. Knowledge in machining, injection molding, and other manufacturing processes. Knowledge in Lean Manufacturing, Design for Manufacturing, ISO Quality Systems and 8D Corrective Actions. Strong problem solving and decision-making skills. Team player with strategic focus.
Ability to multi-task several assignments. Ability to manage priorities to ensure timely completion of projects. Good oral and written communication skills. Good organizational abilities, attention to detail. Ability to support efforts for continuous improvements in process efficiency and cost reduction. Desired Experience/Skills: Experience in the medical device field or regulatory environment preferred. Self-starter, energizing, results-oriented, and able to multi-task. Excellent cross-functional teamwork, coordination, and communication skills. Ability to meet aggressive reliability, performance, cost, serviceability, and delivery targets.
Results oriented with a high commitment level. Work Environment: Office environment with interaction on manufacturing floor and Engineering Test Lab. About Control Devices, LLC Control Devices, LLC (" Control Devices" or " CD" ) is a leading designer & manufacturer of high-quality flow control valves, condensate removal traps, related components & accessories serving the compressed air, pressure washer, vehicle systems, fire protection, specialty gas, & the industrial, agricultural & food service float valve markets.
CD prides itself in the ability to design, innovate & manufacture flow control valves for custom applications & offers a line of standard products that has grown over the years. CD is based in Saint Louis, MO & its products are sold on a global basis to O. E. M. 's, Distributors & End Users. CD offers competitive compensation, a comprehensive benefits package, paid time-off, steeled-toed shoes reimbursement, casual dress work environment, and a solid 401(k) retirement plan to promote financial security. Control Devices, LLC provides is an Equal Opportunity Employer. We provide equal employment opportunities to all employees and applicants and prohibit discrimination and harassment of any type without regard to race, color, religion, age, interaction, national origin, disability status, genetics, protected veteran status, interactionual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Prepares written inspection plans, procedures and testing instructions. Ensures conformance to customer's quality requirements as defined by the Purchase Order, engineering print and regulatory requirements. Initiate, plan, develop and monitor processes for successful execution of the quality in the manufacturing environment.
Assist in development of work standards and control the inspection process. Audit product and processes to requirements. Assist in training of Quality Inspection personnel. Identify and execute elimination of defects and waste. Assist in maintenance of the Quality Management System. Lots of growth opportunity for the right candidate. ESSENTIAL DUTIES and RESPONSIBILITIES:
Engineering Collaborate with our customers' quality and engineering personnel to determine critical part features and review manufacturability of design during the APQP process.
Make recommendations to modify customer part specifications and tolerances as necessary to support cost effective production. Provide engineering support to operations ensuring consistent application of quality techniques Resolve quality issues of capability, tolerancing, and materials related issues. Resolve quality issues by identifying problems, examining solution options, implementing action plans, and providing resources. Effectively communicate and reinforce our commitment to quality improvement efforts
Develop and submit PPAP documents for new product launches and Annual Validations to meet customer requirements.
Determine when process stability and capability studies should be performed on existing processes. Review and analyze results. Recommend changes to processes based upon findings and perform follow up to verify effectiveness. Participate in the Advanced Product Quality Planning activities to determine appropriate use of existing and new measurement systems during new tool or process design and startup. Coordinate pre-launch production trial run process monitoring. Participate in the development of Failure Mode and Effects Analysis (FMEA). Develop and maintain Control Plans and FMEA's throughout the life of the part.
Facilitate and promote use of appropriate problem solving techniques for effective root cause analysis and successful corrective action. Perform duties in accordance with quality system requirements as the voice of our customers. Coordinate with Sales, Purchasing, Engineering, Production, and Toolroom to resolve customer complaints and concerns. Lead PPM improvement plan for strategic customers. Apply appropriate use of statistical techniques. Determine and apply appropriate Measurement System Analysis tools. POSITION CHALLENGES: Maintaining the integrity of the certified quality system requirements with lean, cost-effective strategies that meet the organization's needs.
Advocating as the " voice of the customer" demanding the highest quality expectations from the organization. Executing the duties of the position such that the focus is largely proactive versus reactive. SUPERVISION EXERCISED: Internal Audit Team ORGANIZATIONAL RELATIONSHIPS: Internal Regularly interact with Materials, Quality, Engineering, Sales, and all Manufacturing functions. External Regularly interact with all levels of customers and prospects.
QUALIFICATION REQUIREMENTS: Minimum Technical Qualifications: Bachelor's degree in engineering, prefer Manufacturing, Mechanical or Plastics. 1-3 years' experience as a quality engineer with 1+ in automotive. Exceptional mechanical aptitude (i. e. intuitive understanding of mechanical processes) Proven track record of driving continuous quality improvement in a manufacturing environment. Previous work experience in a Tier II supplier. Customer quality assurance experience. Previous audit experience. Experience with overseas customer base Preferred Technical/Professional Qualifications: Technical knowledge of injection molding and stamping processes.
Formal training and previous experience as an Internal Auditor. Project management experience. Certified Quality Engineer. Background in GD&T.
ship loose list for shipping. Inspect items received for damage and complete paperwork for warranty claims. Visually inspect units and compare to blueprints for accuracy. Relay issues to supervisors and ensure corrections are made prior to shipping. Add labels and photograph unit.
Ensure all punch list items are addressed with aid of supervisors. Ensure all testing has been executed and meets all submittal expectations. Ensure proper filing of paperwork and organization of photographs of units electronically. Quality Control Associate usually work in noisy factory or construction environments. Most of their time is spent standing, walking around, or on ladders while documenting items
on checklists or taking photographs. Propper protective equipment must be worn while in the factory such as steel toe boots, hard hat, and eye protection. EXPERIENCE: High school diploma or GED, additional technical school or bachelor's degree a plus Computer literate (typing, and experience with Microsoft Word and Excel) Ability to use hand tools and powered tools such as drills Ability to use tape measure Ability to perform basic shop math Ability to read and understand technical specifications including blueprints Understanding of HVAC and electrical a plus Ability to test units including pressure, leak tests, voltage and current readings, tachometer, accelerometer, and thermal readings a
plus.
Bilingual a plus WORKING CONDITIONS AND PHYSICAL REQUIREMENTS Ability to lift at least 50 pounds Ability to work 8 hour shifts with occasional overtime as needed.
Ability to work 5 and at some times 6 day weeks Factory environment
of an article. Your Job You will make a difference to the success of this independently owned business as will be responsible for compliance with all procedures provided by the repair station inspection system as appropriate to any article being inspected, overhauled, repaired, or altered by the repair station.
Compensation We offer a competitive total compensation package, including competitive wages and benefits. based on your years of experience. Please note that applicants for these positions must have current status to work in the United States of America in order to be considered for this opportunity. Want to know what your job may be like - click here Working Hours This is a full-time
(FT) 40-hour-a-week position. Hours will change based on business operational needs and flexibility is required. This position is onsite. Must have the flexibility to work second or weekend shifts.
Experience and Education Requirements A minimum of 3 to 5 years of production inspection experience in aviation is strongly preferred. Experience with business aircraft interior completions/refurbishments, heavy maintenance inspections, and exterior paint processes as applicable. Must possess an A&P Certificate or Repairman Certificate issued by Flying Colours Corp. Minimum of 2 years of inspection experience applying Geometric Dimensioning & Tolerancing (GD&T) Principles and Practices. Comprehensive
knowledge of tasks and responsibilities within their technical area.
Comprehensive knowledge of common inspection measuring equipment including but not limited to surface plates, micrometers, height gauges, radius gages, bore gauges, and dial indicators. Ability to identify procedures and parts using approved data and manufacturer maintenance and parts manuals. Good manual dexterity and adept in the use of precision measuring tools. The Details Primary duties include but are not limited to the following: Achieve the required product quality standards by creating, executing, and reinforcing AS9100 system objectives and processes for interior completions.
Perform in-process and final inspections during production. Acting as the customer liaison for source inspection activities. Maintain a thorough understanding of the content of the Company QSM and RSM. Ensure that inspection items are complied with properly and contain the correct manufacturer AMM and applicable references. Ensure that work packages are filled out properly, and reference correct manufacturer AMM, customer, and/or regulatory references as applicable. Review in process work instructions, procedures, and process specs. Monitors and verifies quality in accordance with control processes.
Recommends improvements and amendments as required. Performs review inspections on aircraft and components to monitor the quality of work performed and the adequacy of standards and equipment. Apply problem-solving techniques to ensure best practices and continuous improvement in quality deliverables. Utilize the appropriate resources to solve day-to-day problems; react quickly to unforeseen events. We look forward to hearing from you.
your skills to grow with a great company? Then, this position is right for you! Quality Assurance Technician I - Batch Record Review Position: Full time Our offer: Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance after 60 days.
3% Safe Harbor contribution to your 401k. Up to a 4% Discretionary Match (like a profit-sharing contribution) to your 401k. Paid Time Off (PTO) Employees eligible first day of employment. 9 Company Paid Holidays (72 hours) each year. Uniforms Provided Foot Protection- annual allowance for all laboratory, maintenance and production employees. 24-hour access to our free, on-site fitness center. We provide Individual development,
on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at work.
Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status. We are committed to recruiting and retaining the best talent in the chemical manufacturing industry. Minimum Requirements High School Diploma or G. E. D. Four years of chemical, medical, or similar manufacturing
experience Knowledge & Experience Requirements Must have a quality and continuous improvement mindset.
Ability to utilize a computer, Microsoft Outlook, and Microsoft Excel. Very high attention to detail and basic math skills. Strong understanding of complex processes and technical equipment. Ability to work in a fast-paced environment while meeting productivity demands. Primary Responsibilities Reviewing and approving all batch record documentation. Ensuring all errors in batch record documentation are appropriately and promptly resolved. Printing batch record documentation requested by manufacturing. Reconciling batch record documentation. Conduct various Quality tasks in the plant environment.
Generate and maintain key performance indicators for management review. Other QA duties as needed.
company? Then, this position is right for you! Quality Assurance-Investigator II Position: Full time Our offer: Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance after 60 days. 3% Safe Harbor contribution to your 401k.
Paid Time Off (PTO) Employees eligible first day of employment. 9 Company Paid Holidays (72 hours) each year. Uniforms Provided Foot Protection- annual allowance for all laboratory, maintenance and production employees. 24-hour access to our free, on-site fitness center. We provide Individual development, on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel
valued, inspired and appreciated at work. Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status.
We are committed to recruiting and retaining the best talent in the chemical manufacturing industry. Quality Assurance- Investigator II Background Works under general supervision of the Quality Assurance Compliance Supervisor in a c GMP regulated manufacturing environment operating under ICH Q7A standards. Employees in positions at this
level perform tasks and duties associated with implementation of and compliance to quality assurance standards set by the organization and its customers with an intermediate competence level working on medium complexity investigations.
Tasks Initiate, track, trend, lead, write, and close all investigations into internal failures and external customer complaints. Drive completion of all corrective and preventive actions in a timely manner. Assist department specific subject matter experts in root cause analysis. Regularly conduct personnel interviews to learn sequence of events in root cause determination. Review test data for chemical analyses as inherent part of investigations.
Develop investigation SOPs, work instructions, and conduct associated training. Ensure proper verification of effectiveness for all corrective and preventive actions. Maintain the corrective and preventive actions database and analyze trends. Work with all aspects of operations (Production, Packaging, Project Engineering, Quality Assurance, Quality Control, Maintenance.) to ensure timely completion of CAPAs. Ability to escalate actions cross-functionally when deadlines are approaching. Participate in daily quality meetings to speak on status of issues and bring awareness to / resolve any developing trends.
Participate in cross functional meetings relating to failures. Assist with creating weekly reports on all open investigations and ensure timely completion of investigations. Assist with creating monthly reports on failure metrics and trends. Assist with training QA Investigators at lower levels. Other duties as assigned. Specifications Bachelor of Science in Chemical Engineering, Chemistry, Biochemistry or related field 3+ years working in a regulated medical/chemical manufacturing environment preferred. Minimum 2-3 years direct experience in conducting investigations, root cause analysis, and execution of CAPAs in an FDA regulated environment.
Knowledge of: c GMP regulations, ICH, medical compendia and FDA expectations. R oot cause analysis and utilization of investigation tools and methods. Basic Mathematics MS Office software package (Broad level) Skill in: Strong critical thinking, analytical thinking, deductive reasoning, and problem-solving skills. Strong technical writing skills and understanding of complex and complicated issues. Data Processing with attention to detail and documentation. Working effectively and efficiently on multiple projects at once.
Working effectively in a team environment. Responding to rapidly changing demands. Ability to: Communicate effectively, orally and in writing. Review, compile and verify technical data and documents. Identify, gather, process and record data accurately. Follow customer, organizational and regulatory standards. Work in a fast-paced environment while meeting productivity demands. Present on issues, trends, and similar events with clear, concise, technical language.
$30.00 to $34.00 per hour. Core benefits include medical, dental, vision, FSA, life insurance, company paid short-term and long-term disability, and 401K with match. The Quality Control Inspector will implement and maintain our quality assurance program. This position assists the QA Manager in performing dimensional and weld inspections, resolving material and fabrication problems, qualifying welders, monitoring welding performance, monitoring cleaning and painting procedures.
Qualifications: Three or more years Fitter/Welder and/or Quality Control experience related to structural steel fabrication Working knowledge of AISC, AWSD1.1, SSPC specifications and codes Knowledge of proper fabrication
methods - cutting, burning, shearing, drilling, assemble, bolting, welding, cleaning and painting Knowledge of proper application of NDE methods - VT, PT, MT, UT, RT Ability to interpret material and fabrication requirements from design drawings, contract specifications and shop detail drawings Ability to troubleshoot situations with a team and a professional attitude Ben Hur is an equal opportunity employer.
All applicants will be considered for employment without attention to race, color, religion, interaction, interactionual orientation, gender identity, national origin, veteran or disability status. "
with other departments regarding Receiving and Quality Control requirements. Record, Disposition and Investigate NCRs and RMAs in a timely manner. Comply with applicable Quality Management System requirements; including Quality Policy, Quality Manual, QMS Procedures, Work Instructions, Forms, Recordkeeping, etc.
Support and fully participate in QMS related activities Participate in cross-training to improve ongoing efficiency and business continuity. Maintain clean and orderly work environment. Participate in end-of-year inventory process and assist in resolution of inventory discrepancies. Perform other tasks as deemed necessary by Supervisor. Qualifications High School diploma or equivalent
education Can effectively execute the above listed duties and responsibilities without limitations Follows written and verbal directions with limited oversight Effectively communicates, reads and writes in English language Able to multi-task with frequent interruptions in a fast-paced environment Can perform and cross-train associates in detail-oriented QC inspection techniques Able to interpret QC technical drawings and diagrams Able to carefully handle fragile items and inspect under microscopic magnification Willingness to work on interdepartmental assignments as required Working conditions The job is performed at our facilities in a climate controlled non-smoking environment.
It requires
a person to work day shift and overtime as peak workload may require.
Physical requirements The job requires standing and sitting for extended lengths of time and the ability to lift and manage packages and products weighing up to 30 lbs. Direct reports None.
Management System (QMS) from ISO9001:2015 to ISO13485:2016 at 3 locations, including one in Costa Rica. This is a critical project for us, as it will enable us to streamline our processes and ensure compliance with the latest industry standards. As the Quality Manager, you will play a key role in driving this initiative forward, and you will have the opportunity to work with a talented team of professionals who are passionate about making a difference in the medical device industry.
This position offers an excellent opportunity for an experienced candidate to advance their career and make a significant impact on the success of our organization. Duties and responsibilities Lead the organization
to establish and continuously improve the Quality Management System; including certification to the current ISO 9001:2015 Quality Management Systems Requirements across multiple sites.
Upgrade the organization to ISO 13485:2016 across multiple sites. Oversee effective deployment of human resources throughout the department. Serve as the ISO Management Representative for the EDC Management Team, including administration of periodic Management Reviews; review and maintenance of the Quality Policy, Quality Manual, QMS Plan and Quality Objectives; and response to external QMS related inquiries. Provide quality management support for all QMS processes, with specific oversight and implementation
responsibility for Nonconformities, Corrective Actions, Document Control, Internal Auditing, and QC Inspection of Image Bundles and Small Diameter Subassemblies.
Performs root cause analysis and works with Production Support to prevent manufacturing defects. Provide QMS Communication and Awareness training throughout the organization; providing daily direction and guidance as needed to ensure accurate and consistent application of QMS processes. Coordinate external audit activities and serve as primary contact for certification and surveillance audits, 3rd party and customer audits. Manage customer complaints, establish trending, implement corrective actions and respond appropriately to all investigation requests.
Reviews daily on-the-floor quality related issues with other applicable department management to determine need for corrective actions. Reviews incoming returned product from customers as either nonconforming product or returns for restock. Works directly with customers on review of nonconforming product to include issuance and management of corrective actions (8D's), as required, and visits to the customer facilities to report on actions taken to address quality concerns. Works with suppliers on incoming product quality issues to include issuance of supplier corrective actions, as necessary.
Works with R&D to ensure all product specifications are developed for new products and maintained throughout batching process and production for all products. Support needs of external customers as needed. Qualifications Minimum of bachelor's degree in relevant business or scientific discipline, or a bachelor's degree and a minimum of four years of related experience Prior leadership experience and maintaining an ISO 9001 certified or comparable QMS. Working knowledge of 6 Sigma and Lean Methodology Working knowledge of process validations Possess strong communication and interpersonal skills to address and resolve issues in a positive manner.
Excellent working knowledge of MS Office products, document control systems and quality management tools. Ability to work without being distracted by internal or external influences to effectively execute the above listed duties and responsibilities. Working conditions The job is performed at our facility at 14062 Riverport Dr. in a climate controlled non-smoking environment. It requires a person to work a standard day consistent with exempt employee expectations, where occasional extra effort may be needed to support the organization's needs.
The position may also require occasional overnight travel.
REQUIREMENTS Three to five years' experience in quality assurance/manufacturing environment B. S. degree in an engineering discipline strongly preferred POSITION REQUIREMENTS AND PREFERRED KNOWLEDGE, SKILLS AND ABILITIES Proficient in use of statistical analysis tools.
Strong problem-solving and analytical skills. Experience leading a team through change. Excellent technical communication skills. Ability to interpret product specifications and drawings. Ability to interpret testing procedures and develop test reports based on findings. Ability to collect, analyze and interpret data. Ability to articulate issues clearly to both technical and non-technical team members. Ability to efficiently
organize and manage multiple priorities Ability and desire to grow in the position and accept more responsibility. Ability to take initiative in providing new ideas to improve process efficiencies.
Ability to maintain consistent attendance, arriving on time and prepared for all shifts, meetings, and appointments. ESSENTIAL RESPONSIBILITIES, EXPECTATIONS, AND BEHAVIORS include, but are not limited to, the following: Support of daily manufacturing goals by managing an in-process and final inspection process. Support implementation of strategic plans and implements QA objectives set by QA Coordinator. Supports and sustains a robust QA inspection process. Assists in management of Company's
general compliance with CPSC regulations, ASTM & other federal, state, & agency regulations regarding product safety and labeling requirements.
Audit Excelligence branded and non-Excelligence branded product for appropriate tracking labels; work with vendors to resolve non-compliance. Audit outbound customer shipments for quality; analyze customer complaints & reviews relevant to physical order shipments; partner with Operations and Customer Service to analyze and resolve quality concerns and customer complaints related to outbound customer packages. Assist Product Development team in evaluating new product samples from vendors; assist to resolve/address specific quality concerns.
Develop concise product specifications in conjunction with Product Development for new products. Coordinate on site vendor inspections by Children's Factory and third-party inspection providers Implement relevant procedures pertaining to the Quality Management Systems (QMS) by managing associated processes and procedures. Review quality data (internal and external) and drive feedback to QA team by establishing an effective improvement plan for defects prevention and achieving QDR (quality data review) goals. Participate and support quality related meetings (internal and external) as required Participate and support implementation of quality improvement initiatives Coordinate and support customer related inspection activities on/off-site as required Participate and support internal audits and external periodic QMS audits Maintain and update QA certifications/records.
Escalate any quality concerns or issues in a timely manner Keeps track of QA trends and regulations to ensure effectiveness and compliance Lead problem solving teams on and off the manufacturing floor Develop and execute Manufacturing Floor audits Manage internal and external testing activities In office attendance is an essential function of this position.
WORKING CONDITIONS The essential functions of this job require the employee to perform the following physical activities: Regular use of PC, laptop, copier, fax, and other general office equipment. Ability to access all areas of the facility to perform essentials functions of the position. Noise level for this environment is low to moderate. Children's Factory is proud to be an Equal Opportunity Employer Children's Factory is an Excelligence Company. Excelligence is an Equal Employment Opportunity (EEO) Employer. We are committed to providing equal employment opportunities to all employees, employment applicants and other covered persons without regard to unlawful considerations of race, color, religion or creed, gender, interaction, pregnancy, gender identity or expression, interactionual orientation, marital status, national origin or ancestry, ethnicity, citizenship status, genetic information, military or veteran status, age, physical or mental disability, or any other classification protected by applicable local, state, or federal laws.
superior products and services. About Nooter/Eriksen: Nooter/Eriksen is an employee-owned company with headquarters in Fenton, MO and Milan, Italy. We specialize in HRSG (Heat Recovery Steam Generator) design, fabrication, equipment, and solutions for clients in the power industry, worldwide.
We offer a flexible work schedule with the option of working half-days on Fridays! We provide a full benefits package. Our 401(K) provides an employer match and an annual non-elective contribution. We provide medical with an employer contribution toward the HSA. Dental and Short-Term disability is 100% covered by the company. We also offer vision and fitness reimbursement. We pride ourselves on our
collaborative environment where employees are empowered to advance their career, explore career paths, and grow personally and professionally. DAY IN THE LIFE: The Manager of Quality Control reports directly to the Director of Supply Management and will analyze quality systems to ensure that risk to Nooter/Eriksen is mitigated within market economical constraints, interpret third-party quality backssments of fabrication, installation and operational quality issues, and supervise the Quality Department personnel, including quality and welding engineers and assistants.
As the Manager of Quality Control you will lead the department by communicating company and department goals, setting clear
expectations and actively coaching/developing staff; ensure that the Source Inspection process effectively reduces risk and minimizes cost due to fabrication errors, promote resolution of Quality issues with Supplier, and monitor all quality issues to ensure systematic problems are addressed; supervise the execution of Nooter/Eriksen's Quality Plan and ensure that required certifications are renewed from year to year for continued operations; develop new Quality requirements to meet company goals and develop customer relationships both at the project level and management level, proactively work with department heads to create a high-performance team, and engage with industry organizations that provide support to our quality efforts and provide an avenue for input into quality requirement changes; and travel 10-15% by car or plane.
KEY QUALIFICATIONS. We want the person selected for this role to be successful! The following qualifications are essential to be effective in this role: Four-year degree in engineering is strongly preferred. In lieu of an engineering degree, a four-year degree in a technical field with relevant work experience may be considered. Seeking at least eight (8) years of experience in quality, ASME Section I or VIII, heavy industry, manufacturing, construction, welding, non-destructive testing, and/or other similar fields.
At least three (3) years of experience leading and managing direct reports. Ability to read, write, problem solve, make quick decisions, interpret data and analyze results; effective written and verbal communication is essential. If you are interested in this position, please simply click the Apply button to get started! Our application is quick and should take you less than 5 minutes to fill out. Your information will be then sent directly to the Recruiter. Nooter/Eriksen is committed to creating and maintaining an environment in which all employees feel valued, included, safe, and empowered to do their best work.
We are proud to be an equal opportunity workplace and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, interactionual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics. Pre-employment drug screen and background check required. Job Posted by Applicant Pro
regulatory standards.
Quality Inspectors support manufacturing and servicing operations by performing incoming component and in-process product inspections using standard measurement equipment. They identify, segregate and document rejected material and participate in Material Review Boards to ensure the proper documentation and disposition.
They may also review other related Quality documentation such as device history or calibration records.
with Salesforce is desired, but not required. Job Title: QA Automation Tester Location: REMOTE (w/quarterly reimbursed travel) from approved states only: Alaska, Arizona, Colorado, Delaware, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Maryland, Missouri, New Hampshire, New Mexico, North Carolina, Ohio, Oklahoma, Rhode Island, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Wyoming Role Type: W-2 Only, No C2C Contract Length: 12+ months w/potential extension/conversion Pay: up to $50/hr.
How to Apply: Please send resume and contact information to Keena Leo Sourcing Specialist, at xyz X@ and reference job #233033. DUTIES AND RESPONSIBILITIES: Position involves the automation
and execution of test cases using Smartbear Test Complete software. Responsible for automation of test cases involving multiple applications in support of a major corporate initiative spanning several different business lines.
Work with development teams to ensure quality and stability of software releases. Assist in test data preparation, development of meaningful test scenarios and plans across multiple environments. Strive to optimize the QA process by automating the work where possible. Experience in all phases of testing for both Agile and Waterfall SDLC preferred. QUALIFICATIONS: Must be a US Citizen or Green Card holder. Five or more years of development experience using
Java Script required. 2 or more years' experience directly working with Smart Bear Test Complete software or other test automation software preferred.
Bachelor's Degree from an accredited University in Computer Science, Management Information Systems, Mathematics, or related degree in Engineering, Business, Computer or Science is required. Proficiency working with Microsoft Office Visio, Excel, and Word required. Experience with test management tools such as QTest or Microfocus/HPQC/HPALM or others preferred. Salesforce experience desired. PDN-9adbc715-f66dc8f8ed6d10
