Methods Machine Tools, Inc. supplies high-quality, high-precision machine tools and automation solutions, and designs integrated custom machining processes and systems. Headquartered in Sudbury, Mass., and in operation since 1958, Methods provides an end-to-end portfolio of best-in-class products, engineering, service, parts, training, and integration.
Methods has more than 300 employees, nine technology centers, one high precision machining center, and has installed in excess of 45,000 machines throughout North America.
We currently have the following career opportunity available reporting into our Sudbury, Mass., headquarters.
POSITION OVERVIEWThe ISO Quality Specialist will manage the coordination and improvement of key aspects of the quality management system (QMS) at Methods Machine Tools, Inc. This position works independently and with direct guidance from the Quality Manager to develop and administer methods, tools and practices to achieve quality goals and requirements, including the implementation of ISO 9001:2015 throughout all Methods offices.
This role requires experience in ISO 9001:2015, conducting internal audits, analyzing information, writing and reviewing process documentation, and promoting process improvements. Additionally, experience as an ISO lead auditor, in document control, and corrective/preventive action (CAPA) is preferred.
RESPONSIBILITIESAssists in maintaining the QMS and ensuring adherence to Methods company requirements and the ISO 9001:2015 standard.Lead Auditor for Internal Audits.Planning the Internal Audit schedule and coordinating with the Internal Audit team.Trains personnel in corporate requirements and those of ISO 9001:2015.Management of the CAPA program including root cause analysis and gathering evidence of effectiveness.Management of the Document Control program, ensuring documents are thoroughly reviewed and approved prior to publication.Coordinate the annual review of documents by process owners.Assist in reducing machine inspections through the implementation of better process controls and documentation.Working with team members to create process maps and procedures.Participation in quality system improvement projects as required.Other duties as assigned.SKILLS AND CAPABILITIESAbility to read and interpret domestic and international quality/regulatory standards related to our products.Demonstrates judgment commensurate with experience regarding application of regulatory requirements to data review, reports, design changes, risk management, etc. to ensure compliance and achieving business objectives.Recognition of when to escalate issues to management or consult with more senior staff members.ADDITIONAL REQUIREMENTSAttention to Detail: Ability to pay close attention to detail is required.Accuracy: Work is accurate and complete.Performance Standards: Demonstrated ability to meet department goals.Communication: Excellent written, verbal and presentation skills.Discretion: Acts with integrity in all situations and can maintain appropriate confidentiality.Multi-Tasking: Ability to manage multiple priorities and support changing business needs.Collaboration: Ability to work within a team to bring best solutions to the team or customer.Independence: Self-motivated; works under minimal supervision.Professionalism: Must demonstrate professionalism during all interactions within company, customer and third parties.Takes Initiative: Serves as a role model for "Quality First" by continuously improving on what matters most to customers.Problem Solving: Promptly and effectively handles issues and problems.Decision Making: Makes decisions based on data and risk determination.COLLABORATIONEmployee Health and SafetyFacilitiesFinancePlanningProductionPurchasingServiceEDUCATION AND EXPERIENCEMinimum Knowledge & Experience required for the position: Education: Bachelor of Science in Business, Advanced Manufacturing or related fields, preferred.Experience: A minimum of 2 years of experience in an ISO quality system.Additional Skills/Knowledge:Certifications or experience in – ISO 9001, Internal Auditing, process mapping.Project management (PMP, LSS, Agile, etc.).Experience with SharePoint, Microsoft Teams, ServiceNow, the Microsoft suite of products including Visio.Language: English.Travel Requirements: Up to 20% as required.WORK ENVIRONMENTThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job:While performing the duties of this job, the employee is regularly required to communicate.Must be able to detect, identify and inspect scientific data.The employee will be required to stand and/or walk up to 8 hours per day and/or sit for up to 8 hours per day.Must be able to use hands to feel objects, including keyboard, telephone and pipettes or other lab equipment.May need to reach with hands and arms, climb stairs, balance, stoop, kneel or crouch.Will be required to talk and hear and have specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.May occasionally have to lift and/or move up to 50 pounds.The noise level in the work environment will vary but is usually moderate.This position is very active and requires varying levels of mobility.Methods Machine is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Start your journey to a new and exciting career at Methods.
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