Quality Manager Lisboa

Quality Manager
Lisboa
Lisboa, Lisboa, Portugal

**Summary**Under the direction of the Sr. Manufacturing Engineer Manager, the Quality Manager coordinates, implements, and manages the quality assurance function to the requirements of current ISO and ASME Standards. **Key Responsibilities**This list of duties and responsibilities is not
- inclusive and may be expanded to include other duties and responsibilities as management may deem necessary from time to time. * Lead the quality assurance team to ensure the meeting or exceeding of quality standards. * Establish and implement quality procedures and specifications, testing procedures, and standards for raw materials and for
- process and finished products. * Audit quality systems, initiating corrective action as required. * Develop and recommend inspection and sampling techniques and quality assurance plans. * Develop process control procedures ensuring production of finished products meeting quality specifications and standards. * Develop training requirements and train employees on quality related practices, policies, procedures, and systems. * Produce quality reports; analyze information, and address and resolve problem areas. * Develop and lead
- functional teams to address and resolve quality issues and to improve levels of quality and productivity. * Provide technical assistance to customers, vendors, and other departments of the company. * Conduct research on product defects and recommend modifications to the production process where warranted. * Review all complaints received from customers to determine corrective action. * Develop and maintain departmental budget; ensure maximum utilization of resources within budget constraints. * Ensure compliance with UL, NSF, DOE standards* Ensure compliance with all housekeeping procedures and all quality and safety regulations. * Perform other related duties as assigned. **Education and Experience**A bachelor's degree in a relevant field or a combination of education and experience may be considered. * Five (5) to seven (7) years of supervisory experience* Five (5) to seven (7) years of related quality management experience* Experience in Advanced Product Quality Planning (APQP) and Production Part Approval Process (PPAP). **Qualifications**To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. * The ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, and governmental regulations. * Knowledge of ISO 9001 requirements preferred* The ability to read and interpret part prints and GD&T. - Geometric Dimension and Tolerancing* The ability to write reports and correspondence. * The ability to effectively present information and respond to questions from management, customers, vendors and other employees of the organization. * The ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry and trigonometry. * The ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. * The ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. * The ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. **Physical Requirements*** The ability to talk or hear. * The ability to sit for extended periods of time. * The ability to stand, walk; and use hands to finger, handle, or touch objects or controls. * The ability to occasionally lift and/or move physical products, reports, files, etc. * The ability to use close vision, depth perception, and the ability to adjust focus. **Travel** Up to 10% travel as needed. **ESOP Distributions*** An ESOP is an Employee Stock Ownership Plan. Like mentioned above, Leer Inc. is 100%
- owned. That means **you*** Generous Paid Time Off (Starts at 3-Weeks in 1st Full Year)* 11 Paid Holidays* Health Insurance (Subsidized by Leer)* Dental Insurance* Vision Insurance* Short-Term Disability Insurance (Paid by Leer)* Long-Term Disability Insurance (Paid by Leer)* Life Insurance (Paid by Leer)* 401(K)* Shoe stipend for steel toes* Leer Gear* Cares Program - up to 50% off fitness equipment or gym membership* Community involvement hours**About Leer Inc. **Be part of making iconic products that make all the difference in hospitals, restaurants, and more. We’re proud to be an essential business and support other industries who keep us healthy and fed. Leer, Inc. is a growing company that is all about our team members. Really. We’re 100%
- owned. *As an
- owner at Leer Inc. , you’ll have a direct stake in our success. Through our employee ownership program, you’re not just part of the team, you’re an owner helping to shape our future. We value initiative, collaboration, and a
- term mindset, and we reward your contributions with shared growth and equity. ***Next Steps**If you like what you see here, it’s time to apply! Right below this there’s a big, blue “Apply” button. Click it and apply!Okay, we think you can take it from here. We look forward to meeting you!Under the direction of the Sr. Manufacturing Engineer Manager, the Quality Manager coordinates, implements, and manages the quality assurance function to the requirements of current ISO and ASME Standards.

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