Sr. Process Improver Controls

Published: September 12, 2018
Location
South Region, Puerto Rico
Job Type
Category
Job Code
23006
Years of Experience
5
Travel
No
Education
Bachelor’s Degree
Contact
Rima Murray
Contact Email
rmurray@careersincpr.com

Description

  • Designing and programming of Process Automation Improvement systems.
  • Programming & troubleshooting PLC’s and SCADA systems
  • Providing guidance and support to Control Technicians and Process Improver Controls engineers
  • Leading technical solutions that increase utilization and reduce costs
  • Developing Visual basic C ++ applications for Process Improvement
  • Minimizing service interruptions and avoid unplanned downtime on manufacturing lines
  • Developing process and regulatory documentation for automation systems
  • Performing and documenting engineering studies
  • Improving accuracy of Automation System requirements and specifications for the development of SCADA and other systems.
  • Reviewing/Modifying Standard Operating Procedures for Engineering Controls.
  • Assuring compliance with Laws & Regulations.
  • Submitting documentation for safety compliance, new equipment calibrations, calibration extensions and preventive maintenance.
  • Systems & equipment PM’s SOP’s revisions and/or improvements.
  • Evaluating needs for infrastructure and start-ups.
  • Early Involvement in Transference Effort with Technical Innovations (ROI)
  • Early Involvement in LS /Optimization Efforts with Technical Innovations
  • Assuring Readiness of Manufacturing Requirements for the Optimization Efforts
  • Assuring Compliance with Laws & Regulations
  • Vacations & Overtime Administration for Non- Exempt
  • Generate Purchase Requisitions

 

Requirements

  • Five to ten years of experience with similar responsibilities in a regulated industry (medical devices/pharmaceutical highly desirable)
  • Bachelor's degree in Engineering (Industrial, Chemical, Mechanical, Electrical and/or Computer)
  • Master's preferred, Engineering - In - Training (EIT) licensed.
  •  Knowledge of FDA current GMP/QSR regulation
  •  Excellent oral and written communication skills in both English and Spanish languages
  • Teamwork and service oriented
  • Effective leadership
  • Computer literate (PowerPoint, Word, Excel)
  • Willing to travel

 

 

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