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Quality Technician
Pharmaceutical/Document Deviations
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Location: central, MO
Pay Rate: Contract: 28 to 35.63 $/hr
Salary: 58.24 to 74.11 K$/yr
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Position Type/ Job Duration: Contract 3 - 4 months
Education Required: BS Engineering/Technical 
Years Experience Required: 4

Industry:
Consumer Products
Job Posted: 11/12/2017
Should I worry about this date?
Apply Deadline: 12/4/2017
Job #: 131222NWP
Job order status: Client is actively seeking candidates
Relocation available: Per Diem Available


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QUALITY CONTROL SPECIALIST for Deviation Preparation and Closure 3 month contract opportunity in Columbia, MO. Need BS Degree ansd 4 years experience. Includes per diem and mileage if eligible.

Responsibilities

  • Verify data entry into Batch Production Records and supporting documentation.
  • Ensure that equipment and instrumentation are within calibration/certification due dates. Identify and alert Supervisor of issues on instruments and/or test executions; make initial recommendations for possible solutions and/or corrective actions.
  • Perform regular reviews of equipment log books to ensure completeness of entries and conformance to relevant operational procedures.
  • Operate analytical instrumentation (i.e. HPLC, Bacterial Endotoxin, AES).
  • Log and maintain all references and standards used to support QC testing.Assist in the writing and updating of test procedures, protocols, log books, and checklists.
  • Perform incoming inspection of raw materials and components. Perform environmental monitoring in accordance with all applicable standards.
  • Assist in the execution of all microbiology protocols. Ensure that suitable written records and work undertaken are kept in accord with cGMP and company procedures.
  • Assist in maintaining accurate QC lab and production inventories and order supplies as needed. Assist in the maintenance of the QC lab and production areas which includes routine housekeeping activities.
  • Receive, distribute, track, and coordinate cGMP samples for testing.
  • Participate in internal assessments and regulatory audits as required.

Requirements

  • Bachelor Degree in physical or chemical science
  • 4 to 5 years of experience in GMP in a pharmaceutical environment
  • A PLUS to have Radiopharma industry experience

Benefits

  • Pay rate in range shown based on extent of qualifications
  • Projected 3 to 4+ month assignment
  • Contractor benefits
  • Per diem and mileage if eligible
 
 
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