Manufacturing Engineer

JR Italy; Varese; In loco; EUR 40.000 - 80.000; Tempo pieno

Descrizione del lavoro

An innovative firm is seeking a skilled Manufacturing Process Engineer to enhance healthcare solutions. This role involves managing design transfers to production for medical devices, ensuring compliance with quality standards, and leading continuous process improvements. Join a passionate team dedicated to creating impactful healthcare devices and enjoy a dynamic work environment that values your expertise and contributions. If you have a strong background in medical device manufacturing and a drive to innovate, this opportunity is perfect for you.

Competenze

• 5+ years in medical device manufacturing or similar field.
• Knowledge of plastic injection molding processes is a plus.

Mansioni

• Lead design transfer to production and validation of new manufacturing processes.
• Foster a culture of continuous process improvement focusing on quality and efficiency.

Conoscenze

Medical Device Manufacturing

Process Improvement

Project Management

Communication Skills

Analytical Skills

Formazione

Bachelor's or Master's Degree in Engineering

Strumenti

MS Office Suite

Descrizione del lavoro

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Creanova - Create & Innovate Healthcare solutions for a better quality of life

Location:

Job Category:

Other

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EU work permit required:

Yes

Job Reference:

642526511769636044833712

Job Views:

2

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

Create & Innovate Healthcare Solutions for a better quality of life.

Creanova is a leading B2B partner in Medical Device Development & Contract Manufacturing, specializing in innovative (electro-)medical devices with plastic injection molded enclosures.

For our facility in Como, we are seeking a highly skilled Manufacturing Process Engineer to join our dynamic growing team.

You will be responsible for managing the design transfer to production and series-production assembly lines for several medical devices.

Key Responsibilities:

• Lead and manage the design transfer to production and validation of new manufacturing and assembly line processes for the setup of new series-production assembly lines of medical devices, including plastic injection molding and electronics (PCB);
• Manage the entire series-production process of (recurring) internal orders of the production lines under your responsibility;
• Define and implement necessary corrective and preventative actions in response to internal, regulatory, and customer audit requirements;
• Foster a culture of continuous process improvement with a focus on quality, efficiency, and cost-effectiveness;
• Create, review and ensure compliance with Master Batch Records, internal operational procedures, Qualification/Validation plans, protocols and reports, and other essential GMP documents;
• Plan and conduct training and development for employees regarding new processes;
• Collaborate and ensure effective communication with internal departments (e.g., quality assurance, quality control, warehouse) as well as externally with suppliers and customers, to ensure seamless operations and timely release of goods.

Preferred Qualifications:

• Bachelor's or Master's Degree in a scientific, (bio-)engineering, technology or related discipline.
• Minimum of 5 years of experience in medical device manufacturing or a similar field.
• Knowledge of plastic injection molding processes and electronics manufacturing (PCB) is a plus;
• Knowledge of ISO13485 is desirable;
• Advanced computer skills and proficiency in MS Office Suite;
• Valid driver's license (B category);
• Excellent organizational, communication, and analytical skills;
• Proven ability to lead and manage teams, ensuring efficient and successful manufacturing operations.

If you are ready to contribute to our passionate team dedicated to making a positive impact in the healthcare industry, we would love to hear from you! Join us at Creanova and be part of our mission to create innovative healthcare devices.