Mechanical Engineer

Premium Fertility; Torre Pacheco; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

An innovative biomedical company is seeking a Mechanical Engineer to join their R&D Department. This role focuses on enhancing the embryo transfer process through the development of a groundbreaking medical device. You will engage in mechanical design, material selection, and simulation to ensure the efficiency and effectiveness of the Transfer Direct System. This position offers a unique chance to work on cutting-edge technology in women's health, collaborating with a multidisciplinary team and contributing to significant advancements in assisted reproductive technology. Join a motivated team and make a real impact in the field!

Servicios

Opportunity for Professional Growth

Collaborative Work Environment

Engagement in Research Projects

Formación

• Proficient in CAD software with strong knowledge of mechanical simulation.
• Experience in material selection and manufacturing processes is essential.

Responsabilidades

• Design and optimize mechanical components for the Transfer Direct System.
• Collaborate with suppliers and ensure design implementation and cost optimization.

Conocimientos

CAD Software Proficiency

Mechanical Simulation

Material Selection

Manufacturing Processes Knowledge

Supplier Management

Medical Device Regulations Knowledge

Team Collaboration

English B2/C1

Medical Sector Experience

Herramientas

SolidWorks

Inventor

CATIA

FEA Tools

Descripción del empleo

At Premium Fertility, we are looking for a Mechanical Engineer to join our R&D Department.

Premium Fertility is an innovative biomedical company dedicated to transforming the field of assisted reproductive technology. Our mission is to improve pregnancy success rates by addressing the critical challenges in embryo transfer through our groundbreaking Transfer Direct System (TDS). This semi-automated medical device is designed to enhance embryo implantation efficiency, offering a revolutionary approach to in vitro fertilization (IVF).

Key Accountabilities and Responsibilities:

1. Mechanical design and optimization.
2. Design and redesign key TDS components (CEC and CET equipment, consumables, etc.) to improve accuracy, robustness, and ease of use.
3. Select appropriate materials (especially plastics and polymers) and manufacturing methods (injection molding, machining, 3D printing, etc.) based on functional and cost requirements.
4. Employ simulation tools (e.g. FEA) to validate structural strength and mechanical functionality.
5. Participate in the development and execution of verification and validation plans, including durability and biocompatibility testing, where appropriate.
6. Define and document manufacturing and quality control processes to ensure reproducibility and scalability of designs.
7. Collaborate with suppliers, workshops, and/or industrial partners to ensure proper implementation of designs and optimization of costs and timelines.
8. Ensure traceability of design changes and their impact on technical documentation (DHF, DMR, etc.).
9. Write and maintain updated engineering and audit support documentation (ISO 13485, MDR).
10. Explore new manufacturing technologies, advanced materials, and design improvements that increase efficiency, quality, and/or cost-effectiveness.
11. Participate in multi-disciplinary team meetings, proposing solutions that integrate electronics, software, and mechanics for overall TDS operation.
12. Provide support to the Quality and After Sales Service teams in the resolution of mechanical incidents.
13. Participate in the investigation of non-conformities and in the definition of corrective and preventive actions.

Required skills and experience:

1. Proficient in CAD software (e.g. SolidWorks, Inventor, CATIA or others).
2. Strong knowledge of mechanical simulation, stress analysis, and strength of materials (FEA).
3. Experience in material selection and validation (plastics, metallic, etc.).
4. Knowledge of manufacturing processes: injection molding, CNC machining, assemblies, etc.
5. Ability to manage mechanical engineering suppliers and subcontractors.
6. Familiarity with medical device regulations and standards (ISO 13485, MDR) is desirable.
7. Ability to work in a multidisciplinary team, good communication, and focus on continuous improvement.
8. English B2/C1 for collaboration with international teams is desirable.
9. Previous experience in the medical sector would be an asset.

Salary:

The salary range for this position will depend on the suitability of the candidate for the requested profile.

What do we offer?

Participate in a research project framed within women’s health in a highly motivating team.

1. Opportunity for professional and personal growth, as well as the application of knowledge working with colleagues from the same professional field.

Workplace:

Occasional trips to visit suppliers.

Application Process:

If you are interested, we would appreciate it if you could send us your application.