AbbVie's mission is to discover and deliver innovative
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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 .
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 In our Device Development
department within R&D at the Ludwigshafen site, you will be
working in a team of talented people and experienced management
experts. Together, we break through - as Senior Device Mechanical
Engineer (all genders) (fulltime) (permanent) REF: R We are
looking for a Senior Mechanical Engineer to join our Combination
Product Development team to contribute to the development and
launch of exciting new drug / device combination products. Within
Combination Product Development, the Product Engineering group is
responsible for developing products informed by user needs and
product requirements, completing device design & specifications
and ultimately verification and validation activities that result
in robust devices. These devices enable the delivery of AbbVie's
innovative medicines targeted at difficult-to-cure diseases with
the goal of making a remarkable impact on people's lives. As Senior
Mechanical Engineer, you would be part of a multidisciplinary team
of professionals working at the intersection of engineering and
biopharmaceuticals. The problems you would help to solve relate not
only to the function of innovative devices, but also the way in
which they interact with drug products and the human body. If you
are a self-motivated person who thrives on solving complex problems
and are excited by the idea of taking on the toughest health
challenges, this opportunity might be for you. Make your mark:
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.
Qualifications 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 / ISO and Risk
Management (ISO 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. What we offer you: 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 Multiple times,
we have been globally recognized as a "Great Place to Work" and we
are proud to provide our employees with the flexibility to maintain
a healthy work-life balance. We take our impact on the environment
and our communities seriously and therefore focus on giving
something back on a regular basis. We are committed to equality,
equity, diversity and inclusion (EED&I) - a commitment that is
fundamental to us. This includes appreciating different
perspectives, creating an inclusive culture and treating all
employees with dignity and respect. At AbbVie, your individual
contributions count - help us move mountains together. Be a part of
our success, grow with us and accomplish more than you could have
imagined. Sounds like the perfect career opportunity for you? We
look forward to receiving your application All you need is a
complete CV - we will discuss everything else with you in person.
Any questions? Feel free to email us at
- we look forward to hearing from
you PEOPLE. PASSION. POSSIBILITIES. AbbVie Deutschland GmbH &
Co. KG Website Website
T20:59:59.999Z FULL_TIME EUR YEAR
Ludwigshafen am Rhein 67061 AbbVie-Allee