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Validation Engineer - 1848
Job Description:

The validation engineer will perform consulting activities for clients in Life Science, Pharma and Biotech industries. This individual is responsible for performing validation protocols, including writing and execution; calibration, temperature mapping, data interpretation for equipment and writing of SOP’s. Strong technical writing skills are required. 

Responsibilities:
  • Writing of Validation Protocols such as IQ, OQ and PQs
  • Execution of Validation Protocols such as IQ, OQ and PQs
  • Calibration of Thermocouples for Temperature Mapping Studies
  • Use of Kaye Digistrip Recorders and Validator Software for Temperature Mapping Studies
  • Calculation and interpretation of data for Equipment Validation Studies
  • Excel Spreadsheet Generation and Summary Report Writing for PQ studies
  • Review and modify Standard Operating Procedures (SOPs)
  • Generate test procedures to validate new or previously un-validated equipment/processes
  • Participate in and conduct any or all of the following types of validation:
  • Cleaning Validation
  • Process Validation
  • Computer Validation
  • Equipment Validation
  • Commissioning/decommissioning
  • SIP/CIP Validation
  • Risk Assessments
Requirements:
  • A bachelor’s degree in Engineering, Pharmacology, Biotechnology, Chemistry, Bio-chem, Microbiology or other technical science degree. Master’s degree is preferred.
  • One to three years of experience in a regulated industry (preferably FDA-regulated Biotech, Pharmaceutical or Life Sciences).
  • Excellent knowledge of GMP and cGMP requirements.
  • Knowledge of PC computer OS (typically Windows), knowledge of Word and Excel are required
  • Must have strong written and oral communication skills
Job Listing Information
Job Code:
1848
Job Title:
Validation Engineer
Location:
Madison, WI
Number Of Openings:
1
Employment Duration:
Full-Time
Job Type:
Permanent
Job Industry:
Biotech/ Pharmaceuticals
Work Experience:
Experienced
Date Posted:
05/10/2017


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