Description
A high degree of DeltaV experience in a cGMP environment is critical to this role.ESSENTIAL FUNCTIONS:
- Custom DeltaV engineering solutions
- DeltaV code and user interface development and testing
- cGMP documentation (DDS/FRS)
- Interface to third party equipment (modbus, OPC)
- Test system integration of hardware and equipment
- Software Support of customer FATs
MISC. FUNCTIONS:
- Interface with customers to finalize specifications and generate software quotes
- Provide technical support to the Service organization
- SOP Development
- Supporting product releases - User Manual, Training package, etc
ESSENTIAL SKILLS AND EXPERIENCE:
- Education: BS in engineering or computer science.
- Experience: Min 10 years related experience
- Strong DeltaV and iFix VBA experience
- Pharmaceutical cGMP experience
- Ability to thoroughly document and write/execute test specifications
- Experience with various communication protocols (modbus, OPC, Profibus, etc)
- Strong working knowledge of Microsoft Office
- Ability to support multiple tasks and deadlines simultaneously
- Strong written and oral communication skills
- Ability to travel (less than 25%)
ON THE JOB TRAINING REQUIREMENT(S) FOR QMS
- Software SOP Training.
KEYWORDS: DeltaV, Control Systems, Systems, Electronics, Hardware, Pharmaceutical, Biotech, cGMP, Hardware, Software Engineer, Engineering, Engineer, Software
To find out more about Real please visit www.realstaffing.com