Sr. Improver-Process (Proyectos)
at The Cooper Companies
PDA, Provincia Alajuela, Costa Rica -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 07 Jul, 2024 | Not Specified | 08 Apr, 2024 | 6 year(s) or above | Teamwork,Communication Skills,Excel,Qsr,Health Policy,Powerpoint,Interpersonal Skills,Regulated Industry | No | No |
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Description:
Continuously improves the performance of existing manufacturing processes and equipment through a structured approach.
CooperVision is a global leader in the contact lens industry, dedicated to helping improve the way people see every day. Achieving that goal takes the collaboration of team members with wide-ranging skills; from scientists and researchers, to manufacturing and operations experts, to sales and marketing professionals.
At CooperVision, our effort to improve lives begins with our employees. We are committed to developing people as a key global differentiator and our most important asset. We empower employees to succeed, rewarding great thinking and hard work with competitive pay, comprehensive benefits, and with a special focus on wellness. Our commitment to our core values and a diverse, inclusive, employee-centric culture fuel a deeply engaged, high performing organization.
CooperVision employees pride themselves on being proactive, innovative, flexible and friendly. That’s a strong reflection of our corporate culture—and part of the reason CooperVision may be a great workplace for you.
Qualifications
KNOWLEDGE, SKILLS, AND ABILITIES:
- 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
- Excellent interpersonal skills
- Highly Motivated, self-starter and responsible person
EXPERIENCE:
- Six to ten years of experience with similar responsibilities in a regulated industry (medical devices/pharmaceutical highly desirable)
EDUCATION:
- University bachelor’s degree in engineering or Advanced Student in that fields (Industrial, Chemical, Mechanical, Electrical)
- University master’s degree in engineering (Industrial, Chemical, Mechanical, Electrical) preferred
Regulation Requirements
Quality System Responsibilities
- Complies with the Quality System Regulation (QSR)
- Executes job responsibilities as established in the Standard Operating Procedures (SOP)
- Follows the documentation procedures.
Safety & Occupational Health Responsibilities
- Complies with Safety and Occupational Health Policy and procedures.
- Complies with Hazardous Communication program.
- Notifies immediately all accidents or incidents occurred in work area.
- Promotes and maintains a safe working area and notifies any condition he/she may think might cause an accident.
- Participates in the activities of the Safety and Occupational Health Program as requested.
Essential Functions
How To Apply:
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Responsibilities:
ACCOUNTABLE FOR:
- Coordinating production improvements implementation
- Creating troubleshooting guidelines and/or applicable SOPs and equipment maintenance and repair
- Identifying possible causes of variation/ failure/ under performance for Manufacturing.
- Document diagnostics, solution method and impact in troubleshooting for Manufacturing.
- Measuring Process KPIs for improvement
- Analyzing through a structured approach to identify root causes.
- Improving Process KPIs performance
- Developing control mechanism to ensure Process KPIs consistency.
- Designing and Coordinating Engineering Tests/ Q’s
- Executing Engineering Tests/ Q’s
- Documenting and Reporting Results of Engineering Tests/ Q’s
- Assuring Readiness of Manufacturing Requirements for the Product Transfer
- Receiving and Implementing Product and Equipment Transfer
- Observing, Analyzing, Documenting & Recommending the Start-up of Product Transfer
- Assuring Operator and BU’s resources have the Skills and knowledge coming from change due to Optimizations.
- Implementation of Optimization Efforts
- Defining Manufacturing equipment maintenance requirements
- Developing TPM/ PM/ PDM procedures for Manufacturing Equipment
- Verifying TPM/ PM/ PDM tasks effectiveness in Manufacturing.
- Ensuring correct resources are acting upon situation for Equipment Repair
- Correcting troubles in Manufacturing under performance situation using troubleshooting guidelines and/or applicable SOPs
- Measuring Equipment Efficiency
- Identifying Opportunities for Improvements in Equipment Performance
- Implementing Equipment Upgrades and Optimization Changes
- Writing Validation Documentation and Test Protocols
- Documenting all Equipment Changes
- Assuring Compliance with Laws & Regulations
- Generation of Purchases Requisition
- Submitting Scope and Approve Projects
- Submitting Documentation for Safety Compliance, New Equipment Calibrations, Calibration extensions and Preventive Maintenance
- Systems & Equipment PM’s SOP’s Revisions/ Improvements
- Evaluating Needs for Infrastructure Projects and Start-ups
- Submitting MSDS as Required
Quality System Responsibilities
- Complies with the Quality System Regulation (QSR)
- Executes job responsibilities as established in the Standard Operating Procedures (SOP)
- Follows the documentation procedures
Safety & Occupational Health Responsibilities
- Complies with Safety and Occupational Health Policy and procedures.
- Complies with Hazardous Communication program.
- Notifies immediately all accidents or incidents occurred in work area.
- Promotes and maintains a safe working area and notifies any condition he/she may think might cause an accident.
- Participates in the activities of the Safety and Occupational Health Program as requested
REQUIREMENT SUMMARY
Min:6.0Max:10.0 year(s)
Electrical/Electronic Manufacturing
Production / Maintenance / Quality
Other
Graduate
That fields (industrial chemical mechanical electrical
Proficient
1
Provincia de Alajuela, Costa Rica