HireDiversity

West Chester, PA, US

Senior Electrical Engineer-5011121210

Description

Animas Corporation is currently recruiting for a Senior Engineer with Electrical Background for their West Chester, Pa plant.

Animas Corporation, a fully-integrated global company within the Johnson & Johnson family of companies, is an innovator in insulin pump technology, with products such as the ground-breaking OneTouch Ping. The company is experiencing an unprecedented period of strong growth, outpacing the rapid market growth in the insulin delivery category. As part of the Johnson & Johnson Diabetes Franchise, the company's mission is to create a world without limits for people with diabetes. Animas is dedicated to making diabetes management easier through product innovation, exceptional customer support and customized education programs. Our mission is to improve the lifestyle of our patients, reduce the long-term morbidity of the disease and lower healthcare costs.

The Senior Electrical Engineer will support the manufacturing process for Animas products. The position will directly support the identification, investigation and implementation of product, process and system improvements to achieve quality product, high production yields, and low production costs. This will include:

Leading failure root cause investigation, summaries and action plans.

Developing compliance driven technical documentation to support technical studies, verification and validation protocols and reports.

Implementing process improvements for the manufacturing and test processes.
Recommending design improvements.
Support day-to-day production for Animas products

Lead and/or participate on project teams to meet project objectives and milestones.

Analytical Analysis and Problem Solving of electromechanical device, process and/or equipment.

Determine and document nonconformance and Corrective Action/Preventative Action failure descriptions, root cause investigation, and action plans

Develop engineering studies to collect and analyze data around components and processes to determine trends and opportuntites for improvement

Training of manufacturing associates and updating work instructions to ensure consistent levels of quality for the operations

Support Operations division by executing longer-term process improvement projects

Utilize PE methodology inculding DMAIIC and LEAN roadmaps

Engage with component and assembly suppliers to address technical issues causing inefficiencies, waste or potential supply chain interruptions

Support Manufacturing Systems Engineer in the development and validation of test systems (software and equipment)
Support creation of software code for test systems as a part of development/improvement
Transfer test systems from development to full scale manufacturing

Validation strategy, documentation, and management of execution

Validation (IQ, OQ, PQ, GR&R) and completion report development

Advise other engineering personnel on technical aspects of product/process design and the validation of processes.

Project Management

Utilize project plans to manage team towards common goal and update business partners

Measure, analyze and document improvements ($ savings, yield % improvements, efficiency)

Own change management activities

Partner with design engineers, quality engineers and suppliers to develop robust manufacturing processes for new products in development

Assess design for manufacturability, finalizing tooling and process requirements, executing component and assembly qualifications and conducting technical transfer to steady-state operations

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Qualifications


BS in Engineering Discipline is required but aBSEE degree preferred for this role. Minimum 4-6 years relevant experience in one or more of the following is required: electrical or electro-mechanical assembly (preferably medical device), component manufacturing processes (plastics, metals, printed circuit boards), equipment development and implementation, manufacturing process development and implementation, assembly process development and implementation, process validation. FDA Regulated CGMP environment work experience is asset.

Strong analytical and problem-solving skills are required. Effective compliance driven technical communication skills are required.

Ability to organize, charter, plan and execute multiple projects of increasing complexity is requirement.
Ability to partner, collaborate, influence decision making, and lead projects with associates and business partners that result in improvements in operational metrics is required.
Validation (IQ, OQ, PQ, GR&R) and completion report development is preferred.

Six-sigma (Process Excellence) training and certification preferred.

Proficient with MS Office suite of products required. Basic background in programming using C, C+, Visual Basic, LabView or other related programming languages is a plus.

This position will require up to 20% travel both domestic and International

BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.

Primary Location:North America-United States-Pennsylvania-West Chester
Organization: Animas Corporation (6150)