BOOLEAN STRING RESULTS
Description String Industry
Materials Manager Muskego WI (Indeed) (procurement AND production) AND (material or inventory) AND (Lean OR 5S OR Kaizens OR "Value Stream Mapping") title:(Supervisor OR Manager) anytitle:(Materials Manager OR Materials Coordinator) Information Technology & Services
Warehouse Supervisor (PICK OR SHIPPER OR SHIP OR SHIPPING OR PRODUCT OR HANDLER OR STOCK OR "FREIGHT HANDLER" OR “PACKAGE HANDLER” OR PACKAGING OR LOADING OR UNLOADING OR HANDLING OR WARE OR PACK OR RF OR SCANNER) AND ("DATA ANALYTICS" OR "BUSINESS ANALYST" OR "SIX-SIGMA" OR LEAN) AND "LABOR MANAGEMENT" AND ("SUPPLY CHAIN" OR "ORDER MANAGEMENT") AND (SUPERVISOR OR SUPERVISE OR OPERATOR OR MANAGER OR HANDLER OR LEAD) Warehousing
• Understand, maintain, and contribute to the improvement efforts with document management processes for the BD Interventional Surgery; includes ensuring proper document templates are used, documents undergo appropriate review and approvals, documents are published with high quality standards; documents are appropriate circulated, and acknowledgements are accurately retained and well organized. • Serve as subject matter expert for document management solution. Support efforts for implementation, training, troubleshooting, user-requests, and transition as needed. • Prepare and maintain documents that support company and QA initiatives, such as process documents, policy documents, SOPs, templates, forms, tracking spreadsheets, meeting minutes, etc. • Maintain quality document systems (e.g., EDMS, LMS, EPR etc.). • Understand, maintain, and contribute to the improvement efforts with record management processes for the organization; includes ensuring record retention conventions and list are maintained and communicated, archiving room protocols are followed, and QA files are organized and maintained. • Support QMS/QA related processes as directed. These activities are likely to include the following: Audits, CAPAs, improvement initiatives, Document Control, Record Control, Safety, QMS/Compliance Awareness and Training, Management Review, etc. • Support customer audit/visit efforts as directed. • Recommend quality improvements and suggestions. • Must be able to work with different departments and individuals and help establish reasonable processes and programs to ensure compliance with all industry regulations and standards. • Other duties and tasks that may be assigned on an as-needed basis. • Strong interpersonal, communication and customer service skills. • Excellent technical writing, grammar and speaking skills; ability to create and edit written material in a clear, concise, and accurate manner. • Strong data analysis, problem analysis, and problem-solving skills. • Ability to encourage progress, promote concepts, and maintain confidentiality. • Strong attention to detail and appreciation for organization/order. • Experience planning, organizing and implementing solutions that are sustainable. • Willingness to actively collaborate, work independently, adapt to changes and changing priorities, and work under deadlines without sacrificing accuracy. • Good time management, prioritization, judgment, and decision-making skills. • Expert level knowledge of EDMS and LMS Systems. • Experience with and/or quality systems / quality control compliance / ISO 13485 activities and or facilitating adult learning sessions, preferred. • Industry specific experience preferred. • Knowledge of tools, concepts and methodologies of QA preferred. • Certifications that may include: Document Management Certified Professional, American Society of Quality (ASQ) Certified Quality Improvement Associate, Quality Auditor, or Six Sigma Green Belt, or similar. (Quality or QA or QMS) And (Document or Documentation or DMS) AND (Control or Maintenance or Development) AND ( EDMS or LMS or EPR ) And ( Record or Report or MBR ) AND( MS-Office or Excel or Word or Outlook) And( SOP)AND( CAPA ) AND(ISO 13485)AND((Lean or sigma or KAIZEN or Kanban or 5s or Green belt ) AND( Medical Devices ) Medical Device