Career Based Positions include:

  • Subject Matter Experts
  • Project Managers / Leaders
  • Regulatory Compliance Specialists
  • Quality Assurance Engineers / Specialists
  • Validation Engineers / Specialists
  • Computer Systems Validation Engineers / Specialists
  • Automation Engineers
  • Commissioning, Validation, and Qualification
  • Utilities and Facilities Qualification
  • Cleaning Validation
  • Process Validation, Technology Transfer
  • Chemist / Microbiologist with investigations experience
  • CAPA Knowledge
  • IT and MES Professionals
  • Network Consultants
  • Technical Writers / SOP Translators

Requirements:

  • B.S. or B.A. degree in engineering, science or related fields.
  • Two+ years experience in commissioning, validation, or quality assurance aspects for Pharmaceutical or Healthcare industries.
  • Working knowledge of FDA cGXPs,  US FDA, UK MCA, EMEA, Australia TGA, ANVISA, DCGI, DEA and other local regulatory regulations / guidelines, GAMP.
  • Knowledge of development of Installation, Operational and Performance qualification documents for validation of laboratory or manufacturing equipment, utilities, associated control system, IT application software, enterprise systems.
  • Experience in execution of IQ, OQ and PQ protocols for systems.
  • Experience in development of Standard Operations Procedures, and Summary documents.
  • Knowledge of MS Office Suite, database, and spreadsheet software packages.
  • Willingness to travel within the United States as well as other countries as may be required for duration of up to 12 months.
  • Effective written and oral communication skills.

for Openings in USA, Canada, Ireland email resume to:  resumes@valoitinc.com

for Openings in Puerto Rico, Mexico, South America email resume to:  la@valoitinc.com

for Openings in India, China, Singapore email resume to: asia@valoitinc.com

Please include 3 references details when applying.

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