- Mid-level individual contributor on a project or work team, 3-5 years of experience required.
- Bachelor Degree in Engineering
- Experience within Medical Devices and/or Pharmaceutical industries.
- Experience in equipment IQ, OQ and PQ, Validation, CSV & Process Validation Lifecycle, Technical Writing, and SOP Development.
- Quality Mindset
- Delivers work of significant scope and makes changes in systems and processes to solve problems . Additional Requirements:
- Ability to use statistical and engineering techniques to analyze data and processes.
- Computer literacy in MS Word, Excel, PowerPoint, preferably experience with Minitab
- Ability to speak, write and understand English to comply with written procedures, instructions, SOPs and other documents
- Works with minimum supervision.
-
Assoc Engineering Specialist
hace 21 horas
Weil Group, Inc Villalba, Puerto RicoMinimum RequirementsEntry-level individual contributor on a project or work team. 0-3 years of experience required. · Bachelor Degree in Engineering · Validation, Computer software validation and Technical writing knowledge · Delivers work of limited scope, typically smaller, les ...