Future Opportunities - Join Our Talent Pipeline for R&D Device Engineer - Mechanical, Electrical, or Software Engineer

At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more. Our goal is to consistently provide our customers with innovation, education, exceptional service, and a commitment to excellence, all with a personal touch. For more information, visit . Follow Allergan Aesthetics on LinkedIn.

Job Description

Thank you for considering a future opportunity with our company! We are not currently hiring for this specific role, but we would love to connect with talented individuals who are interested in potential future positions. By joining our talent pipeline, you will be the first to be notified when suitable opportunities arise.

In this talent pipeline requisition, we are not actively recruiting for this position at the moment. However, we are building a network of exceptional individuals who possess the skills and experience required for future openings. By submitting your application to this requisition, you will be added to our talent pipeline and considered for future opportunities.

The Device Engineer will work collaboratively with a team to design and develop medical products from initial concept through the transfer to production. The engineer will have a technical leadership role for designing and testing components and subassemblies of the overall system product. Skills for thermal or structural analysis as well as statistical analysis are needed. He or she develops a thorough understanding of design requirements to ensure that the system's objectives are properly defined and ultimately achieved.

Essential Duties and Responsibilities include the following (other duties may be assigned.):

• Act as a technical lead for product development projects. Provide mentoring and guidance to other team members.
• Manage the overall development of parts and subassemblies for a project design. Interact with Clinical and Marketing departments to determine design requirements and goals.
• Outline and execute to short-term goals to achieve overall project milestones.
• Conceive, design, build, and evaluate prototypes to explore a range of design concepts.
• Prepare, present, and document designs at technical reviews.
• Refine and develop selected concept(s) with little guidance from manager.
• Investigate and evaluate materials, adhesives, and assembly techniques based product requirements and based on past experience.
• Select vendors for prototypes, request quotes and prepare purchase requisitions. Provide recommendations for production vendors.
• Use best methods of design for manufacture and assembly (DFMA) and document the DFMA benefits of the chosen design.
• Plan, perform, and document verification testing. Coordinate testing by other team members,
• Help develop assembly procedures and assist in transfer methods to manufacturing.
• Document ECO changes within the Document Control system.
• Coordinate design tasks for other team members for complex product designs.
• Coordinate design constraints within ME team and other R&D groups. Resolve any design conflicts with preferably no managerial intervention.

Qualifications

• BS in Mechanical, Software, Electrical Engineering or equivalent degree. Advanced degree desirable.
• Must have at least eight years of product design and development experience; prefer ten years of experience.
• Prefer at least three years of experience in medical devices, ideally class II devices.
• Individual will complete work with minimal supervision of the manager. Will typically be the technical leader.
• Proficient with basic standard concepts and constraints involved in creating new product designs. Should be knowledgeable of new modern methods for making prototype or production parts.
• Ability to set medium term project goals and outline schedules for multiple tasks for several team members.
• Strong team player with the demonstrated abilities and willingness to wear "multiple hats" and perform a wide range of tasks within a dynamic environment.
• Individual must have strong verbal and written communication skills.

Additional Requirements:

• Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies.

Additional Information

Applicable only to applicants