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Senior Validation Engineer / Specialist
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Full-time
- In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.)
- What You'll DoWrite C/Q/V documents following established standards and templates, including but not limited to the following:Commissioning FormsC/Q/V Protocols and Summary ReportsStandard Operating ProceduresImpact AssessmentsSpecifications (URS/FRS/DDS)FATS/SATsPerform field/site activities including, but not limited to, the following:Attend and witness FATs and SATs as a representative of IPS clients.
- Primary responsibilities include C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medical device industries.
- The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas.
- About UsIPS, a Berkshire Hathaway Company, is a global leader in developing innovative business solutions for the biotechnology and pharmaceutical industries.
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