Senior Scientist, Engineering II
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Job Location:
North Chicago, IL - USA
Monthly Salary:
Not Disclosed
Posted on:
08-11-2025
Vacancies:
1 Vacancy
Job Summary
Purpose:
We are looking for an experienced and versatile Senior Scientist II/Mechanical Engineer to join our Injection Device Development team to help us accelerate AbbVies combination products from proof-of-concept through submission industrialization and launch.
Our team has end-to-end accountability for commercial development submission industrialization and marketed product support for injection devices that enable the delivery of AbbVies innovative medicines. In the course of our work we collaborate with early-stage CMC Quality Assurance Regulatory Affairs Internal and External Manufacturing and other cross-functional colleagues to ensure timeliness robustness and market success.
As a Senior Scientist II/Mechanical Engineer at AbbVie you will be part of a multi-disciplinary 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 injection systems but also the way in which they interact with drug products and the human body. You would be responsible for advancing programs that combine proven delivery systems with viable commercial drug assets. If you are a self-motivated person who thrives on solving complex problems and are excited by the idea of putting life-changing therapies in the hands of patients this might be the opportunity for you.
Key Responsibilities:
Create and maintain product design documentation
Lead design transfer and industrialization activities
Initiate and lead product design changes and continuous improvement effort
Design and execute laboratory studies supporting product development and on-market investigations
Conduct analytical modeling of key performance attributes of designs
Perform 3D and 2D CAD development in PDM environment
Protocol development documentation of results and authoring of summary reports
Collaborating with third party developers and suppliers
Position required up to 25% of travel time
Preferred Qualifications:
BS in Mechanical or Biomedical Engineering (MS preferred PhD aspirational)
10-12 years of experience (MS 8-10 years PhD 2-4 years) ideally in the medical device drug delivery or other regulated industry
Strong communication skills (both written and verbal)
Strong design and analytical skills
Experience with:
Design controls (in accordance with ISO 13485 / CFR 820.30)
High volume manufacturing processes
3D CAD modeling detailed engineering drawings product database management environment and GD&T
Laboratory environment experiment planning material control and recordkeeping
Technical protocol and report writing
Statistical analysis
Physical prototyping (including 3D printing manual machining etc)
Toolroom environment
Knowledge of material properties material selection and testing methodologies
The 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
Qualifications :
- Bachelors Degree or equivalent education and typically 12 years of experience Masters Degree or equivalent education and typically 10 years of experience PhD and typically 4 years of experience.
- Possess thorough theoretical and practical understanding of own scientific discipline.
- Effective writer and communicator of research or other regulatory materials.
Additional Information :
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at thetime of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic locationand we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.
This job is eligible to participate in our long-term incentive programs
Note: No amount of pay is considered to be wages or compensation until such amount is earned vested and determinable. The amount and availability of anybonus commission incentive benefits or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys soleand absolute discretion unless and until paid and may be modified at the Companys sole and absolute discretion consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Key Skills
- Laboratory Experience
- Mammalian Cell Culture
- Biochemistry
- Assays
- Protein Purification
- Research Experience
- Next Generation Sequencing
- Research & Development
- cGMP
- Cell Culture
- Molecular Biology
- Flow Cytometry
About Company
AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more
