Material Management Specialist Resume

SUMMARY

Authorized to work in United States for any employer
Troubleshoot various inconsistencies with materials and orders
Pull materials according to work order and requests, stage and inform departments of problems that occur
Use good documentation practices to complete paperwork associated with quarantined and transitional materials, assist QA with material release

PROFESSIONAL EXPERIENCE

Material Management Specialist

Confidential

Responsibilities:

Receive materials according to SOPs for GMP pharmaceutical manufacturing, compare pack lists with inventory management system, enter materials into system, quarantine critical materials
Troubleshoot various inconsistencies with materials and orders
Pull materials according to work order and requests, stage and inform departments of problems that occur
Use good documentation practices to complete paperwork associated with quarantined and transitional materials, assist QA with material release

Document Control Coordinator

Confidential

Responsibilities:

Release documents and forms to QC and Manufacturing departments. Track forms, record test information, file hard copies, scan documents for hard drive storage
Revise, route and track SOPs, record employee
Review d Confidential for completeness and accuracy, sign off on finished forms and documents as appropriate

Specimen Processor

Confidential

Responsibilities:

Collect, prepare, and ship medical specimens, including potentially hazardous specimens, under GLP guidelines for off - site testing
Provide exemplary customer service to hospital staff involved in specimen collection in the form of test results and reports, minimal issue resolution turn around time (TAT), site specific collection details, specimen storage, and test implementation
Compose site specific SOPs and train staff at new and existing sites

Production Associate

Confidential

Responsibilities:

Team-oriented production of scientific media products, specifically agar stacker plates
Setup production apparatuses and automated equipment to properly pour, label, package, inspect, and ensure media purity in a clean room

Manufacturing Associate

Confidential

Responsibilities:

Process animal material from intake to production of intermediate heparin product in a cGMP manufacturing environment (raw material processing)
Inspect and unload tankers, oversee digestion process, separate and collect heparin-rich elution for further pharmaceutical processes

Assistant Scientist

Confidential

Responsibilities:

Perform routine analysis of pharmaceutical drug products to determine content, purity, and degradation properties over a pre-determine span of time
Daily use of various laboratory equipment, glassware, and tools as well as associated computer programs to determine and process test results
Participate in continuous to accurately perform analysis according to in-house and client-based SOPs in a cGMP testing environment

Environment: Laboratory Technician

Associate Scientist

Confidential

Responsibilities:

Assist and perform high throughput biochemical or cellular assays
Aid in key steps to screen customer compounds against kinases and known inhibitors
Progress, pass and harvest specific cells lines to be used in agonist or antagonist assays (including monitoring for endotoxin/mcyoplasma in specific cell lines)

Analyst/Laboratory Technician

Confidential

Responsibilities:

Perform methods and procedures according to client and company protocols to best obtain desired results from individual analytical assays
Document, maintain, convey, and review relevant d Confidential in a detailed manner