engineer

About LaSalle Group LaSalle Group is a boutique consulting firm working with top global life sciences companies, delivering management, operations, quality & regulatory compliance, and talent development solutions. We operate out of our Raleigh-Durham and San Juan offices. What You'll Do As a Maintenance Engineer, you'll be responsible for...

At Jacobs, we're challenging today to reinvent tomorrow by solving the world's most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good. Your impact ...

Description This position will offer you the ability to directly apply your knowledge of thermodynamics, heat transfer, fluid mechanics, and power plant engineering You will be preparing calculations, evaluations, and technical reports to support client recommendations and reviews, and will additionally conduct equipment sizing, optimization...

Job DescriptionSenior Systems Engineer with expertise in Requirements Based Engineering (RBE) and experience with Model-Based Systems Engineering (MBSE) to support the development, design, modeling, and integration of aircraft systems. In this role, you will work within a multidisciplinary team to develop and maintain requirements databases in DOORS NG,...

At Fluor, we are proud to design and build projects and careers. We are committed to fostering a welcoming and collaborative work environment that encourages big-picture thinking, brings out the best in our employees, and helps us develop innovative solutions that contribute to building a better world together. If this sounds like a culture you would...

For Technical Services in the Scientist area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with four (4) years of experience as a Scientist or Engineer within the pharmaceutical or regulated industry. Bilingual (English & Spanish). Project Management skills. Shift: Administrative and according to business needs. ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a...

Summary: We are seeking a motivated and experienced Manufacturing Engineer to support manufacturing operations within a regulated Medical Device or Pharmaceutical environment. The selected candidate will provide technical leadership, execute engineering projects, drive process improvements, and support manufacturing validations...

Summary We are seeking a Quality Engineer to provide Quality Assurance support for day-to-day manufacturing operations within a regulated medical device manufacturing environment. This role serves as the primary Quality representative for the assigned manufacturing line, partnering closely with Production, Manufacturing Engineering,...

Inteldot has over 15 years in the life sciences industry, with operations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.Employment type: Full time and onsite roleRole SummaryThe Manufacturing Engineer supports manufacturing operations by assisting with process...

Summary We are seeking an experienced Senior Manufacturing Engineer to support a product transfer project within a regulated medical device manufacturing environment. The ideal candidate will have strong experience in manufacturing engineering, process validation, technical documentation, and engineering support while working...

For Manufacturing services in the Engineering area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Mechanical, Electrical, Industrial, Manufacturing, or Biomedical Engineering, or a related technical field, and 5–7 years of experience in an FDA-regulated environment. Bilingual (English & Spanish). Project Management...

Descripción de la empresa INNOBAL CORP. es una empresa de servicios de ingeniería con sede en Guaynabo, Puerto Rico, especializada en dar soporte a la industria farmacéutica. Ofrecemos soluciones integrales en Project Management, validación, automatización, ingeniería de proyectos y procesos de fabricación. Trabajamos en estrecha colaboración...

Title: Senior Manufacturing Engineer (Medical Devices) Location: North of Puerto Rico (Open to Puerto Rico Residents) Work Schedule: Onsite Contract Duration: 6 to 12 Months Position Overview Our client is seeking an experienced Senior Manufacturing Engineer to lead manufacturing engineering initiatives within a...

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:...

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:...

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: ...

· Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field. · 5-7+ years in manufacturing engineering, process engineering, validation engineering, or quality engineering within an FDA-regulated environment. · Strong working knowledge of 21 CFR Part 820, GMP, ISO 13485, and...

· knowledge of 21 CFR Part 820, GMP, ISO 13485, and documentation practices required in regulated manufacturing environments. · Electrical and mechanical engineering background applied to automated or semi-automated manufacturing systems. · knowledge of automation/controls, tooling, fixtures, test method development, equipment...

Summary of Role: Typically an individual contributor with responsibility in a professional discipline or specialty. 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. Responsibilities: Conducts a...