Senior Device Mechanical Engineer (all genders)

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AbbVie Deutschland GmbH & Co. KG

Ludwigshafen am Rhein

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Senior Device Mechanical Engineer (all genders)

AbbVie Deutschland GmbH & Co. KG

Ludwigshafen am Rhein

Aktualität: 12.06.2025

Anzeigeninhalt:

12.06.2025, AbbVie Deutschland GmbH & Co. KG

Ludwigshafen am Rhein

Senior Device Mechanical Engineer (all genders)

Über uns:

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. People. Passion. Possibilities. Three words that make a world of difference. More than a job. It's a chance to make a real difference. Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of the tomorrow's unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You've come to the right place!

Aufgaben:

Drive the mechanical design process, ensuring robust, reliable, and user-friendly products through partnerships.
Oversee the development of devices for design verification and validation. Work closely with the development partners and manufacturers to ensure design feasibility and reliability.
Provide technical expertise and mentorship for the organization. Foster a collaborative environment to promote innovation and problem-solving.
Conduct feasibility assessment of different device solutions, including early prototyping, analysis, and lab testing.
Execute feasibility and engineering confidence tests to determine design viability and margin.
Plan the Design Outputs strategy and prepare Design Output deliverables for the DHFs following Design Controls.
Support assembly process development for integrated combination products.
Provide support for design verification (test method development, issue resolution).
Perform root cause analysis and corrective action when required.
Carry out analytical modeling of key performance attributes.
Maintain comprehensive documentation of design processes, specifications, and test results. Ensure compliance with quality management systems and regulatory bodies.
Work with software, electrical, and systems engineering teams, as well as quality assurance and regulatory affairs, to ensure seamless product integration.
Stay abreast of industry trends, new technologies, and regulatory changes. Implement best practices for mechanical design and development.
Some travel required.

Qualifikationen:

This is how you can make a difference:
M.Sc. in Mechanical Engineering, with 10+ years of experience or PhD, with 6+ years of experience.
Demonstrated expert knowledge and experience in more than one discipline in combination product development within the pharmaceutical space.
Experience developing a range of mechanical, electromechanical and software-driven medical devices, preferably in the drug delivery space and subcutaneous delivery.
Detailed understanding of principles and practice of Design Controls (CFR 820.30 / ISO 13485) and Risk Management (ISO 14971).
GMP, regulatory and CTD knowledge considered an asset.
Strong communication skills (both written and verbal) with the ability to present complex information clearly to various stakeholders. Capability to influence without direct authority.
Excellent CAD, mechanical design, analytical and problem-solving skills. Ability to troubleshoot complex mechanical issues. SolidWorks proficiency would be an asset.
Strong knowledge of DfX principles, material properties, material selection and manufacturing processes.
Expertise in computational analysis (FEA, system modeling, tolerance analysis) and descriptive statistics.
Experience with physical prototyping (including 3D printing, machining, etc).
Experience with a wide range of testing equipment and methods.
Ability to create and manage schedules for sub-tasks and work streams for which you are responsible.
A keen eye for identifying project risks and proactively developing mitigation plans.

Wir bieten:

With a diverse work environment where you can have a real impact
With an open corporate culture
With an attractive salary
With an intensive onboarding process with a mentor at your side
With flexible work models for a healthy work-life balance
With a corporate health management that offers comprehensive health and exercise programs
With company social benefits
With a wide range of career opportunities in an international organization
With top-tier, attractive development opportunities
With a strong international network

Berufsfeld

Technische Berufe, Ingenieurwesen Techn. Management, Projektplanung Prozessplanung, Organisation Pharma, Chemie, Med., Biotechn. Techn. Entwicklung, Konstruktion Herstellung, Produktion, Entwickl.

Bundesland

Rheinland-Pfalz

Standorte

Ludwigshafen am Rhein

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Senior Device Mechanical Engineer (all genders)