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Career Based Positions include:
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Subject Matter Experts
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Project Managers / Leaders
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Regulatory Compliance Specialists
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Quality Assurance Engineers / Specialists
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Validation Engineers / Specialists
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Computer Systems Validation Engineers / Specialists
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Automation Engineers
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Commissioning, Validation, and Qualification
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Utilities and Facilities Qualification
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Cleaning Validation
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Process Validation, Technology Transfer
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Chemist / Microbiologist with investigations experience
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CAPA Knowledge
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IT and MES Professionals
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Network Consultants
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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.
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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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