Manufacturing Engineer II(#16703165) at Weil Group Inc
Villalba Municipio, Puerto Rico, USA -
Full Time


Start Date

Immediate

Expiry Date

10 Oct, 25

Salary

0.0

Posted On

11 Jul, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Manufacturing, Change Control, Laboratory Equipment, Oee, Process Validation, Computer System Validation, Medical Devices, Ownership, Performance Metrics, Instructions

Industry

Mechanical or Industrial Engineering

Description

JOB DESCRIPTION

For the job assignment, the resource must have knowledge in Process Validation, Equipment IQ and Computer software validation. Provides technical and sustaining engineering support in a manufacturing area; therefore, investigation and root cause analysis skills are required to solve problems or improve effectiveness of job area (inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality). Knowledgeable on statistical techniques. In addition, the resource needs to be schedule oriented in order to meet projects objectives and assignments without impacting deadlines and it is really important for the resource to have good writing skills and communication skills in English and Spanish to have successful and productive meetings within a cross functional team.
DIFFERENTIATING FACTORS: Established and productive individual contributor. Works independently with general supervision on larger, moderately complex projects / cross functional assignments. Delivers and/or manages tasks assigned and works with other stakeholders to achieve desired results. Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision making.
Weil Group is proud to be an Equal Employment Opportunity Employer.
Job Types: Full-time, Temporary

Education:

  • Bachelor’s (Required)

Experience:

  • Manufacturing, Packaging and Laboratory Equipment: 2 years (Preferred)
  • Troubleshooting: 2 years (Preferred)
  • Quality / Process Control / Assurance of Medical Devices: 2 years (Preferred)
  • Change control of Medical Devices: 2 years (Preferred)
  • Equipment Commissioning / Qualification : 2 years (Required)
  • Process & Computer System Validation (CSV): 2 years (Required)

Work Location: In perso

Responsibilities

Please refer the Job description for details

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