/Category Medical Device/Engineering
Job ID 2012-5762
Career Level experienced
Location/Division Warwick, RI/Davol
Relocation No
Posted Date 7/19/2012
Close Date ..
R. Bard, Inc. (NYSE: BCR)is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare.
We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded.
Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world.
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More information about this job:Advanced Manufacturing Engineer / Sr. Advanced Manufacturing Engineer
Davol Inc.
Warwick, Rhode Island
The Advanced Manufacturing Engineer/Sr. Advanced Manufacturing Engineer will be responsible for detailed project management, engineering support and direction for manufacturing activities to support projects for maintenance of business and cost improvements.
Summary of Position with General
Support maintenance of business (MOB) team design activities including:
Concept development and PPS input
Project plans/schedules
Design reviews and design for
Plan, coordinate and manage all manufacturing activities to maintain legacy products including:
Concept and development of methods and processes in support to the plant
Coordination of new tooling and equipment in support to the plant
Coordination and support of new vendor tooling and molds in support to the plant
Development and release of product and process documentation support to the plant
Planning, ordering and management of component inventory in support to the plant
Qualification and validation of new operations and processes including DOE's validation protocol writing, execution, data analysis and executive summary reports in support to the plant
Changes to legacy products cost estimates in conjunction with the plant
Support preparation of the AFE with the plant
Evaluation and recommendation of new
Plan, coordinate and manage all activities to transfer products from design to manufacturing including:
Development and management of a transition plan and team
Documentation, methods and labor standards review
Component inventory transition plan
Facility selection, coordination & preparation
Equipment moves and installation
IQ, OQ, PQ protocol development and execution.
Validation and training support
Basic
BS Degree in Mechanical, Chemical or Biomedical
AME - B.S. degree in Engineering and 2 years relevant experience. With an MS degree, a minimum of 1 year relevant
Senior AME - B.S. degree in Engineering with minimum of 5 years relevant experience. With an MS Degree, a minimum of 3 years relevant
Experience in medical device
Ability to travel
High level of written and verbal communication
Ability to conceptualize ideas, motivate and focus individuals and teams and drive projects through completion on time and on
Understanding and ability to execute DOE, Process validations, and Test method
Understanding of GMP's and medical device regulations as they apply to manufacturingAdditional Desirable Qualifications Skills And Knowledge
- Experience in processing collagen medical devices is preferred.
MS degree preferred.
