Lean Manufacturing Sample Clauses

Lean Manufacturing. Consultant will conduct audits and inspections of work-flow of the operation and implement lean manufacturing practices to eliminate waste (time, process, labor) within the operation.
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Lean Manufacturing. It is the intent of labor and management to promote a culture of continuous improvement. To this end, all products new and existing will be produced in keeping with lean manufacturing principles. At the time of introduction of a new product or re-configuration of an existing product, the manpower and skills requirements will be identified and assigned to meet the planned production hours to manufacture the product. The employees assigned to the team will perform tasks required to support, manufacture and ship the product. By applying Lean Manufacturing Principles, it is our objective to: • Create a sense of ownership among workers. • Make improvements an expectation of workers. • Create a structure of teams to utilize workers’ ideas. • Be open to new ideas from teams. • Provide workers with training required to improving technologies and strategies. • Support teams as partners in improvements. • Encourage a culture that permits change and experimentation to improve our processes. In all these matters we recognize mutual support reflects mutual success. These commitments have been developed to enhance the collective bargaining procedure, not to replace it and will not supercedesupersede other articles of this agreement. Bargaining unit work boundaries will be respected and maintained.
Lean Manufacturing. It is the intent of labor and management to 43 promote a culture of continuous improvement. To this end, all products new and 44 existing will be produced in keeping with lean manufacturing principles. 45 46 At the time of introduction of a new product or reconfiguration of an existing product, 47 the manpower and skills requirements will be identified and assigned to meet the 48 planned production hours to manufacture the product. The employees assigned to 49 the team will perform tasks required to support, manufacture and ship the product. 50 51 By applying Lean Manufacturing Principles, it is our objective to: 52 53 • Create a sense of ownership among workers. 54 55 • Make improvements an expectation of workers. 56 • Create a structure of teams to utilize workers’ ideas. 1 • Be open to new ideas from teams. 3 • Provide workers with training required to improving technologies 5 and strategies. 6 • Support teams as partners in improvements. 8 • Encourage a culture that permits change and experimentation to 10 improve our processes. 11 12 In all these matters we recognize mutual support reflects mutual success. These 13 commitments have been developed to enhance the collective bargaining procedure, 14 not to replace it and will not supersede other articles of this agreement. Bargaining 15 unit work boundaries will be respected and maintained. 16
Lean Manufacturing. (Including 5S) 1. People level. o Through continual education and training so as to increase the level of comprehension of applying lean programmes and tools. o Through consultation with the Team Leaders Team in implementing lean improvements. 2. Process level. o Via the adoption of the Company’s lean vision and strategy both parties shall promote and participate in the identification and elimination of waste. o By using lean manufacturing fundamental tools, such as 5S, visual controls, standardized work practices, total productive maintenance and quick set-up programmes and processes. o By always looking to flow the manufacturing process so to improve such things as process flexibility, production, inventory and materials handling. 3. Performance level. o Through recording and displaying relevant, timely and accurate information on performance. This information shall provide the basis for continuous improvement activities. Goals: To improve DIFOT, production lead times, labour efficiency and waste reduction – including production waste, water and energy.
Lean Manufacturing. Upon Statement of Work (SOW) issuance and prior to commencement of production planning, Seller's executive management will; A. Host a Boeing Lean Supplier Development Specialist (SDS) visit and participate in a facility-wide Lean Diagnostic if not previously conducted by Boeing and host follow-on visits as specified by the Subject Matter Expert (SME). B. Use their best efforts to implement the SDS's recommendations, particularly those tied directly to or in support of 7X7-X production C. Provide a Lean Manufacturing Implementation Plan or modification to an existing plan that is inclusive of all Boeing work and contains a section specific to 7X7-X. The 7X7-X section must demonstrate incorporation of Lean Manufacturing concepts within the following part/assembly development and implementation phases; 1. Part/Assembly design (if Seller has Design Delegation Level 4 or 5 responsibility) 2. Tooling design 3. Production process setup (door to door) The non-program specific (company-wide) portion of the plan must address Lean deployment to; a. Recurring training b. Sub tier interface c. Delivery to Boeing d. Manufacturing support organizations (Enterprise Lean) The Seller Lean Implementation plan must be reviewed and determined acceptable by the SDS and Boeing Procurement Team within a jointly agreed schedule. Within one year of commencement of production, Boeing and Seller agree to use the following metrics to establish an enterprise level baseline followed by monthly measurements to evaluate Lean driven cost improvement: (i) Inventory Turns, defined as Annual Costs of Goods Sold/Inventory Value; (ii) Productivity, defined as Annual Sales/Average Employee Count; and, (iii) Asset Turnover, defined as Annual Sales/Total Assets. Additional metrics may be added and evaluated as agreed to by the parties. Where Boeing and Seller can identify areas of improvement, beyond those previously anticipated, identified and documented in the SBP price, the parties will determine the amount of savings, which will result from the improvements and share the savings. Where a savings is identified and documented, the parties agree to reduce the recurring price by that amount determined by the Parties.

Related to Lean Manufacturing

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time. (b) The Supplier shall not change any process, material, component, packaging or manufacturing location without the Purchaser’s express prior written approval.

  • Manufacture 2.1. The LED(s) on the LED module shall be equipped with suitable fixation elements. 2.2. The fixation elements shall be strong and firmly secured to the LED(s) and the LED module.

  • Manufacturing Services Jabil will manufacture the Product in accordance with the Specifications and any applicable Build Schedules. Jabil will reply to each proposed Build Schedule that is submitted in accordance with the terms of this Agreement by notifying Company of its acceptance or rejection within three (3) business days of receipt of any proposed Build Schedule. In the event of Jabil’s rejection of a proposed Build Schedule, Jabil’s notice of rejection will specify the basis for such rejection. When requested by Company, and subject to appropriate fee and cost adjustments, Jabil will provide Additional Services for existing or future Product manufactured by Jabil. Company shall be solely responsible for the sufficiency and adequacy of the Specifications [***].

  • API If the Software offers integration capabilities via an API, your use of the API may be subject to additional costs or Sage specific policies and terms and conditions (which shall prevail in relation to your use of the API). You may not access or use the API in any way that could cause damage to us or the Software, or in contravention of any applicable laws. We reserve the right in our sole discretion, to: (i) update any API from time to time; (ii) place limitations around your use of any API; and (iii) deny you access to any API in the event of misuse by you or to otherwise protect our legitimate interests.

  • Manufacturing License Subject to the terms of this Agreement, including without limitation Section 2.2, Theravance grants to GSK an exclusive license under the Theravance Patents and Theravance Know-How to make and have made API Compound or formulated Alliance Product in the Territory.

  • Product ACCEPTANCE Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User(s) shall have thirty (30) days from the date of delivery to accept hardware products and sixty (60) days from the date of delivery to accept all other Product. Where the Contractor is responsible for installation, acceptance shall be from completion of installation. Failure to provide notice of acceptance or rejection or a deficiency statement to the Contractor by the end of the period provided for under this clause constitutes acceptance by the Authorized User(s) as of the expiration of that period. The License Term shall be extended by the time periods allowed for trial use, testing and acceptance unless the Commissioner or Authorized User agrees to accept the Product at completion of trial use. Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User shall have the option to run testing on the Product prior to acceptance, such tests and data sets to be specified by User. Where using its own data or tests, Authorized User must have the tests or representative set of data available upon delivery. This demonstration will take the form of a documented installation test, capable of observation by the Authorized User, and shall be made part of the Contractor’s standard documentation. The test data shall remain accessible to the Authorized User after completion of the test. In the event that the documented installation test cannot be completed successfully within the specified acceptance period, and the Contractor or Product is responsible for the delay, Authorized User shall have the option to cancel the order in whole or in part, or to extend the testing period for an additional thirty (30) day increment. Authorized User shall notify Contractor of acceptance upon successful completion of the documented installation test. Such cancellation shall not give rise to any cause of action against the Authorized User for damages, loss of profits, expenses, or other remuneration of any kind. If the Authorized User elects to provide a deficiency statement specifying how the Product fails to meet the specifications within the testing period, Contractor shall have thirty (30) days to correct the deficiency, and the Authorized User shall have an additional sixty (60) days to evaluate the Product as provided herein. If the Product does not meet the specifications at the end of the extended testing period, Authorized User, upon prior written notice to Contractor, may then reject the Product and return all defective Product to Contractor, and Contractor shall refund any monies paid by the Authorized User to Contractor therefor. Costs and liabilities associated with a failure of the Product to perform in accordance with the functionality tests or product specifications during the acceptance period shall be borne fully by Contractor to the extent that said costs or liabilities shall not have been caused by negligent or willful acts or omissions of the Authorized User’s agents or employees. Said costs shall be limited to the amounts set forth in the Limitation of Liability Clause for any liability for costs incurred at the direction or recommendation of Contractor.

  • Manufacture of Products All Products marketed through Grantor's Web ------------------------- Site shall be manufactured, packaged, prepared, and shipped in accordance with the specifications and requirements described on Exhibit A hereto as it may be modified from time to time. Quality control standards relating to the Product's weight, color, consistency, micro-biological content, labeling and packaging are also set forth on Exhibit A. In the event that Exhibit A is incomplete, Products shall be manufactured and shipped in accordance with industry standards.

  • Manufacturing Technology Transfer Upon AbbVie’s written request with respect to a given Collaboration CAR-T Product and Licensed Product, Caribou shall effect a full transfer to AbbVie or its designee (which designee may be an Affiliate or a Third Party Provider) of all Materials and Know-How Controlled by Caribou relating to the then-current process for the Manufacture of such Collaboration CAR-T Product and any corresponding Licensed Products (each, a “Manufacturing Process”). Caribou shall provide, shall cause its Affiliates to provide, and shall use Commercially Reasonable Efforts to assist AbbVie in causing all Third Party Providers to provide, all reasonable assistance requested by AbbVie to enable AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to implement each Manufacturing Process at the facilities designated by AbbVie. If requested by AbbVie, such assistance shall include facilitating the entering into of agreements with applicable Third Party suppliers relating to such Collaboration CAR-T Product and any corresponding Licensed Products. Without limitation of the foregoing, in connection with the Manufacturing Process and related transfer: (a) Caribou shall, and shall cause its Affiliates to, make available to AbbVie (or its Affiliate or designated Third Party Provider, as applicable), and shall use Commercially Reasonable Efforts to assist AbbVie in causing all Third Party Providers to make available to AbbVie, from time to time as AbbVie may request, all Materials and Manufacturing-related Know-How Controlled by Caribou relating to each Manufacturing Process, including methods, reagents and processes and testing/characterization Know-How, and all documentation constituting material support, performance advice, shop practice, standard operating procedures, specifications as to Materials to be used, and control methods, that are necessary or reasonably useful to enable AbbVie (or its Affiliate or designated Third Party manufacturer, as applicable) to use and practice such Manufacturing Process; (b) Caribou shall cause all appropriate employees and representatives of Caribou and its Affiliates, and shall use Commercially Reasonable Efforts to assist AbbVie in causing all appropriate employees and representatives of Third Party Providers, to meet with employees or representatives of AbbVie (or its Affiliate or designated Third Party Provider, as applicable) at the applicable manufacturing facility at mutually convenient times to assist with the working up and use of each Manufacturing Process and with the training of the personnel of AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to the extent necessary or reasonably useful to enable AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to use and practice such Manufacturing Process; (c) Without limiting the generality of this Section 4.4.2, Caribou shall cause all appropriate analytical and quality control laboratory employees and representatives of Caribou and its Affiliates, and shall use Commercially Reasonable Efforts to assist AbbVie in causing all appropriate analytical and quality control laboratory employees and representatives of Third Party Providers, to meet with employees or representatives of AbbVie (or its Affiliate or designated Third Party Provider, as applicable) at the applicable manufacturing facility and make available all necessary equipment, at mutually convenient times, to support and execute the provision of all applicable analytical methods and the validation thereof (including all applicable Know-How, Information and Materials Controlled by Caribou, and sufficient supplies of all primary and other reference standards); (d) Caribou shall, and shall cause its Affiliates to, take such steps, and shall use Commercially Reasonable Efforts to assist AbbVie in causing Third Party Providers take such steps, as are necessary or reasonably useful to assist AbbVie (or its Affiliate or designated Third Party Provider, as applicable) in obtaining any necessary licenses, permits or approvals from Regulatory Authorities with respect to the Manufacture of the applicable Collaboration CAR-T Products and corresponding Licensed Products at the applicable facilities; and (e) Caribou shall, and shall cause its Affiliates to, provide, and shall use Commercially Reasonable Efforts to assist AbbVie in causing Third Party Providers to provide, such other assistance as AbbVie (or its Affiliate or designated Third Party Provider, as applicable) may reasonably request to enable AbbVie (or its Affiliate or designated Third Party Provider, as applicable) to use and practice each Manufacturing Process and otherwise to Manufacture the applicable Collaboration CAR-T Products and corresponding Licensed Products.

  • PRODUCT MANUFACTURER'S SUPPLIERS Only those dealers/distributors listed by the manufacturer will be considered authorized to act on behalf of the Product Manufacturer.

  • Commercialization Intrexon shall have the right to develop and Commercialize the Reverted Products itself or with one or more Third Parties, and shall have the right, without obligation to Fibrocell, to take any such actions in connection with such activities as Intrexon (or its designee), at its discretion, deems appropriate.

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