Propagating a Culture of Quality Sample Clauses

Propagating a Culture of Quality. The Quality Manager supports the development of strategic quality management vision for product development and manufacturing. The Quality Manager ensures that quality assurance is an inherent part of the product development pipelines as well as an organization’s corporate culture. The responsibility extends beyond implementing a quality management system (QMS), writing manuals, filing for regulatory approval and performing audits. A Quality Manager ties in QMS policies, SOPs, regulatory requirements and enforcement into every aspect of an organization’s business process. He or she constantly drives, monitors and improves compliance by using quality-at-source methodologies and applying appropriate key performance indicators.
Sample 1
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Propagating a Culture of Quality. The Director of Supply Chain supports the quality team in the development of strategic quality management vision for product development and manufacturing. The Director of Supply Chain supports the quality team in ensuring that quality assurance is an inherent part of the product development pipelines as well as an organization's corporate culture. The responsibility extends beyond implementing a strategic sourcing plan, a quality management system (QMS), writing manuals, filing for regulatory approval and performing audits. A Director of Supply Chain ties in sourcing and inventory metrics, QMS policies, SOPs, regulatory requirements and enforcement into every aspect of an organization's business process. He or she constantly drives, monitors and improves compliance by using quality-at-source methodologies and applying appropriate key performance indicators associated with supply chain and inventory management.
Sample 1
Propagating a Culture of Quality. The CQO provides strategic quality management vision for product development and manufacturing. The CQO ensures that quality assurance is an inherent part of the product development pipelines as well as an organization’s corporate culture. The responsibility extends beyond implementing a quality management system (QMS), writing manuals, filing for regulatory approval and performing audits. A CQO ties in QMS policies, SOPs, regulatory requirements and enforcement into every aspect of an organization’s business process. He or she constantly drives, monitors and improves compliance by using quality-at-source methodologies and applying appropriate key performance indicators.
Sample 1
Propagating a Culture of Quality. The Director of Regulatory Affairs supports the quality team in the development of strategic quality management vision for product development and manufacturing. The Director of Regulatory Affairs supports the quality team in ensuring that quality assurance is an inherent part of the product development pipelines as well as an organization's corporate culture. The responsibility extends beyond implementing a strategic sourcing plan, a quality management system (QMS), writing manuals, filing for regulatory approval and performing audits. A Director of Regulatory Affairs supports the team in tying in sourcing and inventory metrics, QMS policies, SOPs, regulatory requirements and enforcement into every aspect of an organization's business process. He or she constantly supports the team in driving, monitoring and improving compliance by using quality-at source methodologies and applying appropriate key performance indicators associated with regulatory standards.
Sample 1
Propagating a Culture of Quality. The Director of Quality supports the development of strategic quality management vision for product development and manufacturing. The Director of Quality ensures that quality assurance is an inherent part of the product development pipelines as well as an organization’s corporate culture. The responsibility extends beyond implementing a quality management system (QMS), writing manuals, filing for regulatory approval and performing audits. A Director of Quality ties in QMS policies, SOPs, regulatory requirements and enforcement into every aspect of an organization’s business process. He or she constantly drives, monitors and improves compliance by using quality-at-source methodologies and applying appropriate key performance indicators.
Sample 1

Related to Propagating a Culture of Quality

  • Product Quality (a) Tesoro warrants that all Products delivered under this Agreement or any Purchaser Order shall meet the latest applicable pipeline specifications for that Product upon receipt at the applicable Terminal and contain no deleterious substances or concentrations of any contaminants that may make it or its components commercially unacceptable in general industry application. Tesoro shall not deliver to any of the Terminals any Products which: (a) would in any way be injurious to any of the Terminals; (b) would render any of the Terminals unfit for the proper storage of similar Products; (c) would contaminate or otherwise downgrade the quality of the Products stored in commingled storage; (d) may not be lawfully stored at the Terminals; or (e) otherwise do not meet applicable Product specifications for such Product that are customary in the location of the Terminal. If, however, there are Products that do not have such applicable specifications, the specifications shall be mutually agreed upon by the Parties. Should Tesoro's commingled Products not meet or exceed the minimum quality standards set forth in this Agreement or any applicable Purchase Order, Tesoro shall be liable for all loss, damage and cost incurred thereby, including damage to Products of third parties commingled with Tesoro's unfit Products.

  • Manufacture (a) Manufacturer shall only manufacture the specific number of Products as requested by Company and at no time shall manufacture excess goods or overruns. Manufacturer shall not sell any Products bearing the Trademarks to any third parties without the express written consent of Company.

  • Manufacture of Product Prior to commercialization of the Product, the Parties may, if appropriate for both parties, negotiate in good faith a manufacturing and supply agreement to provide for Licensor to fulfill the manufacturing requirements of Licensee for Product for sale in the European market. The cost of such manufacturing shall not be greater than * percent (*%) of the cost of any competitor cGMP contract manufacturing facility that proposes to manufacturer the Product for Licensee. * Confidential information has been omitted and filed confidentially with the Securities and Exchange Commission.

  • 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.

  • 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.

  • Development of Products (a) During the term of this Agreement, ViewRay may from time to time seek services from PEKO with respect to the development of certain Products that can be incorporated into the ViewRay Renaissance™ MRI-guided radiation therapy system. For each Program to be undertaken by PEKO pursuant to this Agreement, the parties will prepare a “Work Statement” and agree to said “Work Statement” in substantially the form attached as Attachment 1. Each Work Statement will describe: (i) the (i) services that PEKO will be responsible for providing to ViewRay and the deliverables that PEKO will be responsible for delivering to ViewRay (“Deliverable(s)”), (ii) delivery schedule for the Deliverables, (iii) pricing terms, (iv) work plan for the Program, and (v) ViewRay’s responsibilities in connection with the Program. Each Work Statement will be prepared based upon the requirements and information provided to PEKO by ViewRay. A separate Work Statement will be required for each Program; and each Work Statement will become subject to this Agreement only when mutually agreed and signed by ViewRay and PEKO.

  • Manufacturing Intrexon shall have the option and, in the event it so elects, shall use Diligent Efforts, to perform any manufacturing activities in connection with the Aquaculture Program that relate to the Intrexon Materials, including through the use of a suitable Third Party contract manufacturer. To the extent that Intrexon so elects, Intrexon may request that AquaBounty and Intrexon establish and execute a separate manufacturing and supply agreement, which agreement will establish and govern the production, quality assurance, and regulatory activities associated with manufacture of Intrexon Materials. Except as provided in Section 4.1, any manufacturing undertaken by Intrexon pursuant to the preceding sentence shall be performed in exchange for cash payments equal to Intrexon’s Fully Loaded Cost in connection with such manufacturing, on terms to be negotiated by the Parties in good faith. In the event that Intrexon does not manufacture Intrexon Materials or bulk quantities of other components of AquaBounty Products, then Intrexon shall provide to AquaBounty or a contract manufacturer selected by AquaBounty and approved by Intrexon (such approval not to be unreasonably withheld) all Information Controlled by Intrexon that is (a) related to the manufacturing of such Intrexon Materials or bulk qualities of other components of AquaBounty Products for use in the Field and (b) reasonably necessary to enable AquaBounty or such contract manufacturer (as appropriate) for the sole purpose of manufacturing such Intrexon Materials or bulk quantities of other components of AquaBounty Products. The costs and expenses incurred by Intrexon in carrying out such transfer shall be borne by Intrexon. Any manufacturing Information transferred hereunder to AquaBounty or its contract manufacturer shall not be further transferred to any Third Party, including any Product Sublicensee, or any AquaBounty Affiliate without the prior written consent of Intrexon; provided, however, that Intrexon shall not unreasonably withhold such consent if necessary to permit AquaBounty to switch manufacturers.

  • Quality Quality matters related to the Manufacture of the Compounds shall be governed by the terms of the Clinical Quality Agreement in addition to the relevant quality provisions of this Agreement.

  • Products 1.1. The information (including but not limited to the quantity, rated hashrate, unit price (“Unit Price”), total price for one item (“Total Price (One Item)”), total price for all the items (“Total Purchase Price”) of Products to be purchased by Party B from Party A is as follows (“Products”):

  • Licensed Products Lessee will obtain no title to Licensed Products which will at all times remain the property of the owner of the Licensed Products. A license from the owner may be required and it is Lessee's responsibility to obtain any required license before the use of the Licensed Products. Lessee agrees to treat the Licensed Products as confidential information of the owner, to observe all copyright restrictions, and not to reproduce or sell the Licensed Products.

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