המקום בו המומחים והחברות הטובות ביותר נפגשים
West Pharma Projects Analyst Brazil, São Paulo 30519115
23.11.2025
Essential Duties and Responsibilities
- Ability to modify and test machine vision systems and components, including the ability to write and revise software configurations.
- Ability to troubleshoot, diagnose, repair, improve vision system mechanical, hardware, software components.
- Provide support to current and future projects as related to vision operations.
- Apply and support lean manufacturing initiatives, identifying vision eject reduction opportunities through process improvements, tuning of configurations, or other strategies. Help Improve the speed and reliability of vision system changeovers.
- Assist in the implementation and maintaining the vision control strategy through accurate project records and Gantt charts and other tools.
- Actively participate and comply with all West HSE programs and regulations.
- Maintain a neat and orderly work environment in accordance with West 5S program.
- Performs other duties as assigned based on business needs as directed by Vision Inspection Supervisor, Engineering Manager and/or Director, Ops.
Education
- Bachelor's Degree Engineering required
Work Experience
- Minimum 3 years experience within vision inspection related field preferred
- Automation, Programming (PLC, VBA), Electronics Troubleshooting preferred
- Vision machine integration in a cGMP/Pharmaceutical manufacturing environment. preferred
- Application skills utilizing latest software, hardware, and vision technology preferred
- Project management, ability to work independently required
Preferred Knowledge, Skills and Abilities
- General knowledge of OSHA/EPA/safety regulations, manufacturing, and process automation.
- Maintain an awareness of “state of the art” technology as it applies to our industry. Take part in educational programs pertinent to process projects.
- Working knowledge of business and shop floor systems to effectively manage operations; prefer SAP and MS Office applications.
- Experience working with ISO9000, FDA and cGMP required.
- Understanding and experience in use of Lean manufacturing principles.
- Ability to write routine reports, correspondence, and process documents.
- Excellent organizational and communication skills.
- Works independently with minimal guidance.
- Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
- Able to comply with the company’s safety policy at all times
- Able to comply with the company’s quality policy at all times
משרות נוספות שיכולות לעניין אותך
