Qureos Mentor

Quality Consulting Group

<div>QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you&rsquo;ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico &amp; USA
Responsibilities:<ul><li>
Support the design, development, and implementation of small-scale automated equipment and systems. This role will involve contributing to the design and programming of PLCs, assisting in the integration of vision systems, and supporting robotic automation projects to improve manufacturing processes. The candidate will also assist in creating CAD models, wiring schematics, and ensuring compliance with safety and quality standards.</li><li>
Responsibility in our technical functions to advance existing technology or introduce new technology and therapies.</li><li>
Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results.</li><li>
May act as a mentor to colleagues or may direct the work of other lower level professionals.</li><li>
The majority of time is spent delivering R&amp;D, systems or initiatives related to new technologies or therapies &ndash; from design to implementation - while adhering to policies, using specialized knowledge and skills.</li><li>
Develops and applies computer aided design (CAD) software engineering methods, theories and research techniques in the investigation and solution of technical problems.</li><li>
Assessing architecture and hardware limitations, plans technical projects in the design and development of CAD software.</li><li>
Defines and selects new approaches and implementation of CAD software engineering applications and design specifications and parameters.</li><li>
Develops routines and utility programs.</li><li>
Prepares design specifications, analysis and recommendations for presentation and approval.</li><li>
May specify materials, equipment and supplies required for completion of projects and may evaluate vendor capabilities to provide required products or services.</li></ul> 
Qualifications:<ul><li>
Bachelor Degree in Engineering (Mechanical or Electrical preferred)</li><li>
2+ years of direct application testing experience, preferably within a Windows or Linux desktop environment and including automation.</li><li>
Previous experience in PLC Programming &amp; Controls: Basic to intermediate experience in programming and troubleshooting PLCs (e.g., Siemens, Allen-Bradley) with a focus on learning advanced techniques.</li><li>
Previous experience in Vision Systems &amp; Robotics: Familiarity with vision systems (e.g., Cognex, Keyence) and robotics (e.g., FANUC, ABB), with the ability to assist in system integration and troubleshooting.</li><li>
CAD Design &amp; Wiring: Proficiency in CAD software (e.g., SolidWorks, AutoCAD) and basic knowledge of electrical wiring and schematics, with a desire to expand design capabilities.</li><li>
3D CAD designs</li><li>
Development of the SCADA and HMI applications</li><li>
Develop PLC applications</li><li>
Applied machine Learning</li><li>
Artificial Intelligence</li><li>
Available for 1st shift</li></ul>
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.
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JT663 - DESIGN AUTOMATION ENGINEER II

<div>QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you&rsquo;ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico &amp; USA. 
 
Responsibilities:<ul><li>
Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.</li><li>
Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.</li><li>
Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.</li><li>
Adapts machine or equipment design to factory and production conditions.</li><li>
May incorporate inspection and test requirements into the production plan.</li><li>
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.</li><li>
Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.</li></ul>
Qualifications:<ul><li>
Bachelor&rsquo;s degree in Engineering</li><li>
3+ years of relevant experience.</li><li>
Process/Computer System Validation</li><li>
CAD Electrical Design proficiency</li><li>
PLC/HMI/Vision Programing</li><li>
Shift: 1st shift</li></ul>
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.
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JT923 - MANUFACTURING ENGINEER II

<div>QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you&rsquo;ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico &amp; USA. 
 
Responsibilities:<ul><li>
Change control of Medical Devices</li><li>
Equipment Commissioning / Qualification</li><li>
Process Validation</li><li>
Computer System Validation (CSV)</li><li>
Manufacturing, Packaging and Laboratory Equipment</li><li>
Technical experience (Trouble shooting) or any similar experience or background</li><li>
Quality / Process Control / Assurance of Medical Devices</li><li>
Design and development of a packaging system for terminally sterilized medical devices as per requirements established by ISO 11607-1 (Part 1: Requirements for materials, sterile barrier systems and packaging systems) and corresponding packaging ASTM and ISTA (International Safe Transit Association) standards.</li><li>
Validation of processes for packaging medical devices that are terminally sterilized as per requirements established by ISO 11607 2 (Part 2: Validation requirements for forming, sealing and assembly processes).</li><li>
These processes include forming, sealing and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems.</li></ul> 
Qualifications:<ul><li>
Bachelor&rsquo;s degree in Engineering</li><li>
3+ years of relevant experience.</li><li>
Strong working knowledge of FDA Medical Devices Part 820 Quality System (QS) Regulation &amp; Medical Device Good Manufacturing Practices</li><li>
Process Validation, Equipment IQ and Computer software validation knowledge</li><li>
Technical writing knowledge and Communication skills</li><li>
Investigation and root cause analysis skills</li><li>
Must have knowledge in Process Validation, Equipment IQ and Computer software validation.</li><li>
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).Good writing skills and communication skills in English and Spanish to have successful and productive meetings within a cross functional team</li><li>
Experiences with manufacturing processes creation / improvements</li><li>
Experience with process validations (IQ, PD, OQ, PQ)</li><li>
Special build coordination and follow up in manufacture.</li><li>
Shift: 1st shift and 2nd shift</li></ul>
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.
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JT011 - MANUFACTURING ENGINEER II

Join Quality Consulting Group and explore 3   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Quality Consulting Group

About Company

JT663 - DESIGN AUTOMATION ENGINEER II

JT923 - MANUFACTURING ENGINEER II

JT011 - MANUFACTURING ENGINEER II