Manufacturing Associate
Agilent cedar creekUpdate time: May 27,2020
Job Description
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek ---- so they can do what they do best: improve the world around us. Information about Agilent is available at www.agilent.com.









By delivering high-quality, innovative products to customers when and where they need them, Agilent's Manufacturing Team supports our company's mission to inspire scientists and researchers to make discoveries that advance the quality of life. Join our fast-growing, dynamic organization and be part of this rewarding work.



As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Your proficiency in analytical testing and immunohistochemistry applications will be required to perform in-process quality control on a variety of products.


Primary Responsibility:

  • Maintaining a work environment based on 5S and Lean Manufacturing principles.
  • Work with team to coordinate the manufacture and testing of samples as delivered to meet time frame set by management
  • Identifying opportunities for process improvements.

 

Job Duties:

  • Maintain accurate inventory.
  • Submit electronic MMT for materials required.
  • Perform all processes of manufacturing including Packaging, Aliquots, Fish testing, FFPE Testing, Bravo Processes, Customs, Manual PCR labeling.
  • Assist in training all other employees on manufacturing processes.
  • Work with team to coordinate the manufacture and testing of samples as delivered to meet time frame set by management.
  • Utilize tools to achieve and maintain a zero backlog of materials.
  • Perform verifications on all process types when required to do so.
  • Perform all transactions in SAP required for process orders.
  • Submit Deviation Notices (DN) when required.
  • Record and maintain issues or errors that occur within the manufacturing processes.
  • Assist in the trouble shooting of technical problems that may arise.
  • Assist in the writing, maintenance and reviewing of FDA compliant work instructions (WI) and standard operating procedures (SOP) and other duties as assigned.
  • Answer technical questions about products
  • Assist on required validations of equipment, new raw materials, and process that may be required by group.
  • Learn EBR development process.

 

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