Principal Engineer

AbbVie Device RoleThe focus of this Device role is to design/develop and commercialize semi-assembly and assembly automation solutions for syringe, auto-injector, wearable devices, etc. Organization consists of subject matter experts which have comprehensive knowledge of the commercialization process. This includes process/product development, front end planning, capacity scale-up, capital projects definition and execution, validation, regulatory submissions, and commercial manufacturing. This group has a broad-based understanding of all the relevant areas necessary to develop pharmaceutical products, (drug, device, packaging, and performance).ResponsibilitiesResponsible for compliance with applicable policies and procedures. Ensures quality and effectiveness of key results of major projects within function through sound design, early risk assessments, and implementation of fallback strategies. Has full awareness of the potential consequences (defects and failure modes) of design changes to established processes.Mitigates risk within functions through sound design, early risk assessments and implementation of fallback strategies.Develops, plans, coordinates and directs engineering aspects of projects across multiple locations that are of major scope and importance. Manages multiple, often concurrent projects and meets expectations. Makes difficult decisions regarding priorities among projects.Supports development of project strategy to align and achieve key customer business objectives. Contributes to the development of long-term business and organizational strategies.Works with customer on project approach / design to optimize asset value. Leads cross functional teams in resolving major project hurdles. Reviews constructability strategy. Anticipates and resolves problems and crisis situations requiring fast, astute decisions with rapid implementation by utilizing technical training and / or experience.A Subject Matter Expert in project engineering/project management. Participates on internal, cross-divisional teams to develop and align procedures and standards. Participates on group or divisional task forces. Participates in professional affiliations.QualificationsA Bachelors Degree in Engineering, science, or closely related discipline is desired, or equivalent technical experience plus demonstrated competence, with a desired 10+ years of significant engineering and/or operational experience. A post-graduate education / degree is desired, and may contribute towards the desired years of experience.A career history marked by a consistent series of contributions and accomplishments. Proven track record of managing projects to completion, using extensive external resources.Demonstrated excellence in breadth and depth of knowledge within project management.Interacts well with diverse groups within engineering and maintains strong working relationships with internal and external collaborators.Listens to and understands others' points of view and articulates tactfully and respectfully one's own perspective orally, in writing, and in presentations.Works well with other engineers in a collaborative, fast-paced goal-driven environment.Possesses interpersonal skills to negotiate and reconcile differences.A technical background in health care, medical devices, biological, pharmaceutical, or similar industries (preferred).Demonstrated competency with financial systems and in fiscal control. Project accounting experience.Formal Project Management training (preferred)Additional InformationThe 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 the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and 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 long-term incentive programs.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: Fraud AlertAbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.Protect yourself by verifying job offers and communications. Your safety is important to us.Yes, 15% of the TimePay Range: $109500 - 208500 USDWhere We WorkRole is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.