JT587 - MANUFACTURING ENGINEER II

qualityconsultinggroup; Villalba (PR); On-site; USD 65,000 - 95,000; Full time

Job summary

Quality Consulting Group, LLC in Puerto Rico & USA seeks a talented Engineer to design manufacturing processes, machine layouts, and production procedures for assemblies and equipment. You will drive process development, validation, and documentation to support product quality.

With a Bachelor's in Engineering and 3+ years of experience, you will perform IQ/OQ/PQ, SOP development, change control, and MES-related tasks, including injection molding processes.

Qualifications

• Bachelor’s degree in Engineering.
• 3+ years of relevant experience.
• Process Development and documentation.
• Equipment validation.
• SOP Development.
• Special Build Documentation and Line Support.
• Experience in IQ |OQ |PQ and/or process validation.
• Process Validation Lifecycle (from process characterization, operational qualification to performance qualification).
• SOP Development | Special Build Documentation and Line Support.
• Computer and software validation CSV.
• Change control of Medical Devices.
• MES system.
• Experience in injection molding processes.
• Shift: 1st shift.

Responsibilities

• Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
• Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
• Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
• Adapts machine or equipment design to factory and production conditions.
• May incorporate inspection and test requirements into the production plan.
• 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.
• Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.

Skills

Process Development

Documentation

Equipment validation

SOP Development

Line Support

IQ/OQ/PQ Validation

CSV Validation

Change control

MES system

Injection molding

Education

Bachelor’s degree in Engineering

Tools

MES system

Job description

QUALITY CONSULTING GROUP, a leader inthe pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities

• Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
• Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
• Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
• Adapts machine or equipment design to factory and production conditions.
• May incorporate inspection and test requirements into the production plan.
• 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.
• Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.

Qualifications

• Bachelor’s degree in Engineering
• 3+ years of relevant experience.
• Process Development and documentation
• Equipment validation
• SOP Development
• Special Build Documentation and Line Support
• Experience in equipment IQ |Experience in OQ (Operational Qualification) and PQ (Performance Qualification) and/or process validation
• Process Validation Lifecycle ( from process characterization, operational qualification to performance qualification)
• SOP Development | Special Build Documentation and Line Support
• Computer and software validation CSV
• Change control of Medical Devices
• MES system
• Experience in injection molding processes
• Shift : 1st shift

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.