Validation Consultant
PSC Biotech
1d ago

Validation Consultant - 1842 Responsibilities :

  • Completing work assignments as specified by the Validation Project Manager
  • Providing timely updates to the Validation Project Manager
  • Adhering to the proper site safety practices; wearing adequate safety equipment when required
  • Completing timesheets and expense reports in a timely manner
  • Working in a biotech / pharmaceutical environment as a consultant / contractor to various clients of PSC
  • Working closely with client's employees on various projects and various GMP facilities to help client with validation issues
  • Learning new ideas, techniques and systems
  • Commuting to PSC clients' sites for validation projects
  • Keep client’s proprietary information confidential
  • Authoring Validation Protocols such as IQ, OQ and PQs
  • Executing Validation Protocols such as IQ, OQ and PQs
  • Calibrating Thermocouples for Temperature Mapping Studies
  • Calculating and interpreting of collected data from validation studies
  • Generating Validation Summary Reports and Standard Operating Procedures (SOPs)
  • Create Validation Risk Assessments
  • Requirements :

  • Degree qualification; B.S in Chemical, Life Sciences, Mechanical, or Electrical Engineering
  • Knowledge in GMP facilities and cGMP requirements
  • Preferably with 8 years or more of GMP experience in a biotech or sterile pharmaceutical manufacturing environment, or the equivalent
  • Proficient in computer skills and MS Office applications
  • Knowledge in process control systems (PLC, DCS and / or SCADA) and validation test instruments such as Kaye Validator will be an added advantage
  • High energy and attention to details
  • Excellent written and verbal communication skills
  • A demonstrated ability to work well in a team environment
  • Interested applicants, kindly submit your applicants and attach your updated resume along with your current and expected remmuneration.

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