Location: Iowa City, IA
Company: Loparex
Loparex's Iowa City Facility is currently looking for a Quality Manager. This position manages quality processes and the quality lab for the Iowa City facility. DUTIES Promote safety by leading by example, participating in safety engagements, and encouraging the team to work safe each day and to follow all safety guidelines and procedures.
Cultivate a culture focused on continuous improvement in safety performance. Extensive knowledge with ISO 9001 including prior experience with auditing. Lead by personal example with a positive attitude, setting the standards for the team. Regular review and refinement of supplier and customer specifications. Disposition of non-conforming product. Compile
and distribute internal rejection information. Develop Quality Assurance tests and forms. Responsible for approval and release of final product. Assist with the resolution of process and equipment problems.
Supervisors Quality Engineers and Quality Assurance Assistant. QUALIFICATIONS Bachelor's degree or combination of education and experience to meet requirements. Five (5) to seven (7) years of related experience in a manufacturing environment. Solid computer skills. Ability to communicate professionally, both verbally and in writing. Ability to troubleshoot and strong problem-solving skills. Strong leadership, communication, organizational, and interpersonal skills. Ability to work
with both internal and external customers. Knowledge of extrusion coating, silicone coating, printing and slitting process preferred.
Ability to lead others and give direction in a positive, professional manner. Lean and/or Six Sigma experience or other structured problem solving is desired. Must be able to manage multiple tasks/priorities and easily adapt to changing situations. Must have the ability to wear personal protective equipment, including ear plugs, safety glasses and steel toed shoes. BENEFITS Medical, Dental, and Vision Insurance Telehealth Health savings account with generous annual employer contribution Fitness reimbursement program Development and career growth opportunities Competitive 401(k) matching program We are an equal opportunity employer.
All qualified applicants will be considered for employment without regard to race, color, religion, interaction, interactionual orientation, gender identity, national origin, disability, veteran status, or any other category protected by applicable law.
USA, and locations in Aachen and Berlin, Germany, Tokyo, Japan, and Singapore. Abiomed is part of Johnson & Johnson Med Tech. Abiomed is an employer with attractive working conditions and an appreciative corporate culture that focuses on the needs of its employees.
Abiomed inspires and retains exceptional talent through collaboration, passion and continuous development. Exciting tasks are awaiting you: You will lead the Non-Conformity Management for purchased parts You assure compliance with our SOPs and external regulations during supplier qualifications and supplier related change management Your proactive approach ensures continuous improvements of process and product quality You coordinate
root cause analyses in multidisciplinary teams and apply your methodological skills You ensure quality through supplier audits Your profile: Bachelor's or Master's degree in engineering or technician with work experience.
Professional experience in engineering and/or quality management in the medical technology and/or automotive industry desirable Practical knowledge of FDA QSR, ISO 13485 and ISO 14971 Experience in the application of statistical methods Good Communication skills in German and English and assertive appearance Enjoying teamwork in an innovative and global work environment Abiomed is an Equal Opportunity Employer committed to a diverse workforce. Abiomed will not discriminate
against any worker or job applicant on the basis of race, color, religion, gender, gender identity, national origin, ancestry, age, interaction, interactionual orientation, gender identity, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.
Abiomed maintains a drug-free workplace.
phases company processes. Requirements: Bachelors degree in Quality Sciences, Engineering or comparative work in a technical field. 5-7 years of experience in Quality Management leadership and Quality Engineering in a manufacturing or process environment. Strong preference for quality-related experience in a manufacturing/foundry environment Demonstrated experience in the effective use of quality core tools (APQP, PPAP, FMEA, MSA, SPC, etc.
). Experience in deploying statistical quality methods (sampling plans, DOE, Cpk, etc. ) Understanding of metrology, with the ability to utilize several types of measuring devices such as calipers, micrometers, hardness testing, x-ray and coordinate
measuring machine (CMM). Experience with destructive and non-destructive tests on materials and parts to measure performance, life, or materials characteristics.
Ability to interpret engineering drawings, schematic diagrams or formulas and confer with management or engineering staff to determine quality standards. ISO9001 Quality Management System leadership experience. ASQ Quality Engineer certification a plus. Six Sigma Green or Black Belt Certified a plus. Experience with ISO14001, ITAR, AS9100, TS16942, ISO14981 quality systems. Experience with continuous improvement processes i. e. six sigma, kaizen, lean, etc. SALARY: $90-120K
of harnesses Perform inspection of first article and first piece inspections Aid in the trouble shooting of wire harness assemblies Follow compliance of AS9100 documentation requirements as applied to the wire harness production. Assist in the implementation and compliance of quality department initiatives, programs, policies, and goals.
Contribute in additional quality responsibilities as needed Knowledge, Skills, Abilities: Ability to read and understand technical drawings Mechanical aptitude and abilities preferred Experience with basic test equipment preferred Highly organized with ability to work in a fast pace environment Must have a positive attitude with a customer appreciation mentality Ability to lift 40lbs on a regular basis
Operational Excellence Principal Accountabilities: Compile statistical quality data including defects, product measurement data, and various metrics Maintain a Document Control system with collaboration of document owners Document changes to, and maintain the policies related to, the QMS Participate in organizational process improvement efforts Assist in providing guidance and training on quality best practices to teams across the organization Review customer and regulatory requirements, and provide guidance to the organization regarding compliance Assist in processing of returned material including status tracking and facilitating product return to customers Support in processing of Engineering
Change Notices Assist in verifying effectiveness of implemented Corrective Actions Manage Record Retention program including scanning and filing of various documents for record retention Provide solutions whenever possible Serve as back up to Production Documentation Specialist Additional work projects and responsibilities as assigned Required Skills: Previous experience with AS9100 or Quality in a manufacturing environment preferred Strong analytical and problem solving skills are required Highly organized and detail oriented Must be skilled and accurate in data entry and be proficient in Outlook, Excel, Visio and Word Strong interpersonal skills, including excellent verbal and written communication
skills Ability to perform multiple tasks effectively with a focus of timeliness and responsiveness Must have a positive attitude with a customer-appreciation mentality Bachelor's degree or related work experience required
