Project Engineer - Medical Devices (On-site)

Cronoshare.Com; Cáceres; On-site; EUR 38,000 - 60,000; Full time

Job summary

Becton, Dickinson, and Company (BD) is seeking a Project Engineer to lead engineering initiatives at the ESP Almaraz site in Spain. You will oversee full lifecycle projects, coordinate with R&D, manufacturing, quality, and marketing, and ensure adherence to cost, schedule, and regulatory standards.

The role requires a Bachelor’s in Engineering, 3–5 years of project engineering experience in medical devices or pharma, and strong Spanish/English communication.

Qualifications

• Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical, or related).
• 3–5 years of experience as a Project Engineer or similar role, preferably in medical device/pharma.
• PMP certification or equivalent is a plus.
• Strong communication in Spanish and English.
• Familiarity with FDA regulations and ISO 13485 desirable.

Responsibilities

• Manage full project lifecycle from planning to delivery, including scope, schedule, and resources.
• Collaborate with R&D, Manufacturing, Quality, and Marketing to align with objectives.
• Identify, assess, and mitigate project risks; develop contingency plans.
• Monitor budget and ensure expenditures stay within approved limits.
• Prepare and present project progress reports to stakeholders.
• Ensure compliance with safety, quality, and regulatory requirements.
• Perform technical analyses to resolve issues and optimize performance.
• Develop and maintain detailed technical documentation: specs, drawings, tests.

Skills

Project management

Leadership

Bilingual English/Spanish

Data analysis

Regulatory awareness

Education

Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical, or related)

Job description

Becton, Dickinson, and Company (BD) is seeking a Project Engineer to lead engineering initiatives at the ESP Almaraz site in Spain. You will oversee full lifecycle projects, coordinate with R&D, manufacturing, quality, and marketing, and ensure adherence to cost, schedule, and regulatory standards.

The role requires a Bachelor’s in Engineering, 3–5 years of project engineering experience in medical devices or pharma, and strong Spanish/English communication.