JT025 - PROJECT DEVELOPMENT ENGINEER

Juncos, Puerto Rico

Temporary

Medical Device

Experienced

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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