JT025 - PROJECT DEVELOPMENT ENGINEER at Quality Consulting Group

Juncos, Puerto Rico, United States -

Full Time

Start Date

Immediate

Expiry Date

10 Oct, 26

Salary

0.0

Posted On

13 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Project Development, CAD, CAM, CATIA, ProEngineer, Solidworks, Siemens NX, Agile MAP, SAP, Design Control Systems, GMP Documentation, Medical Device Regulations, Engineering Process Documentation, Product Lifecycle Management, Bilingual Communication, Quality Assurance

Industry

Outsourcing and Offshoring Consulting

Description

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’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: May document engineering processes and specifications. Recommends formats responsive to technical and customer requirements. Produces products that conform to the company documentation and quality assurance standards. Perform all type of design changes target specifications and technology target specifications. Change Originator for PCH's, RCH's, DCH's, QCH's, MCS's in Agile MAP, SAP and Design Control Systems. Reviews product development requirements for compatibility with processing methods to determine product design outputs. Interacts with product design and development personnel to ensure that processes and designs are compatible. Perform change of designs components or portions of systems and modifies existing designs to develop or improve products and facilitate manufacturing and field service operations. Utilizes computer-aided design equipment and/or graphic tools, such as CAD, CAM, CATIA, ProEngineer, Solidworx or Siemens NX Software. Coordinates design criteria with engineering, manufacturing, tooling, material, and planning group such as ease of manufacture, availability of materials, and contractual specifications. Ensures processes and procedures are in compliance with regulations. Formulates, delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. Qualifications: Bachelor's degree in Engineering 2 + years of Engineering experience. Agile MAP / Product Lifecycle experience Bilingual, Communication, Quality mindset Knowledge in Medical Devices regulations. Experience in GMP documentation. Administrative 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.

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Responsibilities

The role involves documenting engineering processes, managing design changes, and ensuring products conform to quality assurance standards. The engineer will coordinate design criteria across various departments and manage assigned projects to achieve desired results.