The Sr. Mechanical Engineer works collaboratively with a team to design and develop medical products from initial concept through the transfer to production. The engineer has some technical leadership for designing and testing components and subassemblies of the overall system product. The job requires CAD skill knowledge, and it is preferred to have some knowledge of designing injection molded parts and machined metal components. The engineer should have knowledge of plastic, elastomer, and metal material types and be able to define the selection criteria and tradeoffs. Candidates should have experience with thermal or structural analysis as well as knowledge of basic statistical analysis methods. Prefer some knowledge in fluid based cooling systems, thermoelectric modules, and biocompatible material selection.
Essential Duties and Responsibilities include the following (other duties may be assigned.):
Apply the principles of Geometric Dimensioning & Tolerancing to all drawings of parts and assemblies.
Conceive, design, build, and evaluate prototypes to explore a range of design concepts.
Prepare, present, and document designs at reviews.
Refine and develop selected concept(s) with guidance from manager, technical, and clinical leaders.
Work closely with other departments and outside entities, e.g. suppliers and contract resources, to insure design and documentation conformance to all quality requirements.
Investigate, evaluate and specify materials, adhesives, and assembly techniques.
Select prototype suppliers, request quotes, prepare purchase requisitions. Provide recommendations for production suppliers.
Create designs for ease of manufacture and assembly.
Document designs and design changes within a medical device document control environment.
Manage the simultaneous development of several parts for a product design. Coordinate design constraints and resolves any design conflicts with minimal managerial or lead engineer intervention.
BS in Mechanical Engineering or equivalent degree. Advanced degree desireable.
8 years min experience of product design or product development or equivalent experience; prefer ten years of experience
Proficient with 3D CAD software design tools for creating solid models and drawings; such as CREO or SolidWorks.
Familiar with software and methods for computer simulation of complex mechanical, fluid, and thermal models.
Individual must be able to work under the general supervision of the manager or a technical project leader.
Familiar with basic standard concepts and constraints involved in creating new medical product designs.
Ability to set short term project goals and outline schedules for specific tasks.
Individual must have strong verbal and written communication skills
Strong team player with the demonstrated abilities and willingness to wear “multiple hats” and perform a wide range of tasks within a dynamic environment.
Chicago, IL
AbbVie Inc. discovers, develops, manufactures, and sells pharmaceutical products in the United States, Japan, Germany, Canada, Italy, Spain, the Netherlands, the United Kingdom, Brazil, and internationally. The company offers HUMIRA, a therapy administered as an injection for autoimmune and intestinal Behçet's diseases; IMBRUVICA to treat adult patients with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), mantle cell lymphoma, waldenström’s macroglobulinemia, marginal zone lymphoma, and chronic graft versus host disease; VENCLEXTA, a BCL-2 inhibitor used to treat adults with CLL or SLL; VIEKIRA PAK, an interferon-free therapy to treat adults with genotype 1 chronic hepatitis C virus (HCV); TECHNIVIE to treat adults with genotype 4 HCV infection; and MAVYRET to treat patients with chronic HCV genotype 1-6 infection.
It also provides KALETRA, an anti-human immunodeficiency virus (HIV)-1 medicine used with other anti-HIV-1 medications to maintain viral suppression in HIV-1 patients; NORVIR, a protease inhibitor indicated in combination with other antiretroviral agents to treat HIV-1; and SYNAGIS to prevent respiratory syncytial virus infection at-risk infants. In addition, the company offers AndroGel, a testosterone replacement therapy for males; CREON, a pancreatic enzyme therapy for exocrine pancreatic insufficiency; Synthroid to treat hypothyroidism; and Lupron to treat prostate cancer, endometriosis, and central precocious puberty, as well as anemia.
Further, it provides Duopa and Duodopa, a levodopa-carbidopa intestinal gel to treat Parkinson’s disease; Sevoflurane, an anesthesia product; and ORILISSA, a non-peptide small molecule gonadotropin-releasing hormone antagonist for women with moderate to severe endometriosis pain. It has collaborations with Alector, Inc.; Janssen Biotech, Inc.; Galapagos; Bristol-Myers Squibb Company; and Calico Life Sciences LLC. The company was incorporated in 2012 and is headquartered in North Chicago, Illinois.