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Clinical supply chain Associate

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Posted : Monday, February 05, 2024 07:50 PM

*Responsibilities:* • With guidance may exercise independent judgment in developing methods, techniques and evaluation criteria for obtaining results.
• Ensures record-tracking of pertinent data is being completed through computerized systems.
• Analyzes non-routine information or data to support Supply Chain activities – e.
g.
, inventory levels, prices and tracking of shipments, inventory positioning, material deliveries, planned master production schedule and sales forecasts.
• Initiates or receives requests for routine changes affecting inventory levels, e.
g.
, shipments, purchases, movement of stock.
Performs necessary transactions and records in system to reflect changes.
• Prepares standard documents, such as work orders, purchase orders, material transfer requests, or shipping documentation.
• Generating the MTRs - Planners on IRT, folder to create the IQS MTRs, coordinate shipment.
) • Tracks progress with department supervisors, readjusts schedules and communicates changes according to production progress, change orders, manpower requirements, product availability or other conditions impacting timelines.
•Uploads of Clinical Supply Chain Documents file documents to the electronic Trial Master File (eTMF) *Knowledge, Experience & Skills:* • Works on assignments that range from routine to semi routine in nature where independent action and initiative are required in resolving problems and developing recommendations.
• Works on assignments where ability to recognize deviation from accepted practice is required.
• Good verbal and written communication skills and interpersonal skills are required.
• Demonstrates a working knowledge with intermediate level proficiency in Microsoft Office applications.
• Able to develop solutions to moderately non-routine problems.
• Normally receives no instruction on routine work, general instructions on new assignments.
• Applies working knowledge of manufacturing and production operations and current Good Manufacturing Practices (cGMPs) daily.
*Basic Qualifications:* 2+ years of relevant experience in related field and a Bachelor’s degree; or 1+ year of relevant experience and a Master’s degree.
*Top 3 Required Skill Sets:* Working knowledge MSOffice suite-Excel, Word and Email; Problem Solver and Communication Skills *Top 3 Nice to Have Skill Sets:* Clinical Supply Chain Management; Working knowledge of Oracle or SAP Job Type: Contract Salary: $40.
00 - $45.
00 per hour Schedule: * 8 hour shift * Day shift * Monday to Friday Experience: * Pharmaceutical/ biotechnology Industry: 3 years (Required) * Clinical supply chain: 3 years (Required) Work Location: In person

• Phone : NA

• Location : 600 Anacapa Ln, Foster City, CA

• Post ID: 9130353137


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