Johnson & Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com.
You can get further details about the nature of this opening, and what is expected from applicants, by reading the below. Job Function: Supply Chain Engineering
Job Sub Function: Project Engineering
Job Category: Scientific/Technology
All Job Posting Locations: US345 MA Danvers - 22 Cherry Hill Dr
Job Description: Johnson & Johnson Heart Recovery (ABIOMED) is looking to hire a Senior Supplier Project Manager in a hybrid role based in Danvers, MA.
Principle Duties and Responsibilities:
Lead project management activities for external manufacturing programs
Attend product development project meetings and serve as primary liaison for all actions associated with supplier requirements as well as coordinating quality inspection
Manage and track supplier-related projects for capacity increase, risk mitigation, obsolescence, and quality improvement
Generate and maintain supply chain program dashboards and report outs for different levels of management
Highlight supply chain risks and develop mitigation plans to achieve successful product launches
Support the transfer of product improvements into suppliers' production utilizing Design for Manufacturing (DFM) principles
Provide project lead for Supplier Engineering team
Manage and develop supply chain phase-in plans accounting for various medical device regulatory approval timelines
Qualify and implement dimensional and visual inspections through GR&Rs at incoming and Supplier
Assist in the "Quality at the Source" program with the objective of increasing yields at the supplier and qualifying quality inspections at the supplier facility
Develop understanding of supplier’s manufacturing process and technology roadmap and capabilities
Drive strategic initiatives with suppliers
Qualify new suppliers and define necessary technical tests/documentation
Perform process validations and verifications of components and sub-assemblies at suppliers
Lead analysis of defective components found in Incoming Inspection and work with vendors to resolve
Assist in technical qualification of alternatives for obsolete components
Qualifications:
BS in Electrical, Biomedical, or other related Engineering disciplines
Successful program management experience, supporting multiple programs in parallel
3+ years of professional experience showing detailed technical exchange with vendors
Knowledge of Process Qualifications, Process Capability, and data analysis using statistical tools
Good knowledge of Six Sigma, Lean and Design of Manufacturing. Six Sigma Green or Black Belt is a +
Demonstrated critical thinking in fast-paced environment
Enjoys working in a team environment while continually and constructively challenging the status quo
Basic understanding of medical device regulatory submissions
Dedicated, passionate and eager to learn
Sound MS Office knowledge
Willingness to travel, particularly to visit suppliers (up to 20%)
The anticipated base pay range for this position is $108,800 to $147,200.
#J-18808-Ljbffr
You can get further details about the nature of this opening, and what is expected from applicants, by reading the below. Job Function: Supply Chain Engineering
Job Sub Function: Project Engineering
Job Category: Scientific/Technology
All Job Posting Locations: US345 MA Danvers - 22 Cherry Hill Dr
Job Description: Johnson & Johnson Heart Recovery (ABIOMED) is looking to hire a Senior Supplier Project Manager in a hybrid role based in Danvers, MA.
Principle Duties and Responsibilities:
Lead project management activities for external manufacturing programs
Attend product development project meetings and serve as primary liaison for all actions associated with supplier requirements as well as coordinating quality inspection
Manage and track supplier-related projects for capacity increase, risk mitigation, obsolescence, and quality improvement
Generate and maintain supply chain program dashboards and report outs for different levels of management
Highlight supply chain risks and develop mitigation plans to achieve successful product launches
Support the transfer of product improvements into suppliers' production utilizing Design for Manufacturing (DFM) principles
Provide project lead for Supplier Engineering team
Manage and develop supply chain phase-in plans accounting for various medical device regulatory approval timelines
Qualify and implement dimensional and visual inspections through GR&Rs at incoming and Supplier
Assist in the "Quality at the Source" program with the objective of increasing yields at the supplier and qualifying quality inspections at the supplier facility
Develop understanding of supplier’s manufacturing process and technology roadmap and capabilities
Drive strategic initiatives with suppliers
Qualify new suppliers and define necessary technical tests/documentation
Perform process validations and verifications of components and sub-assemblies at suppliers
Lead analysis of defective components found in Incoming Inspection and work with vendors to resolve
Assist in technical qualification of alternatives for obsolete components
Qualifications:
BS in Electrical, Biomedical, or other related Engineering disciplines
Successful program management experience, supporting multiple programs in parallel
3+ years of professional experience showing detailed technical exchange with vendors
Knowledge of Process Qualifications, Process Capability, and data analysis using statistical tools
Good knowledge of Six Sigma, Lean and Design of Manufacturing. Six Sigma Green or Black Belt is a +
Demonstrated critical thinking in fast-paced environment
Enjoys working in a team environment while continually and constructively challenging the status quo
Basic understanding of medical device regulatory submissions
Dedicated, passionate and eager to learn
Sound MS Office knowledge
Willingness to travel, particularly to visit suppliers (up to 20%)
The anticipated base pay range for this position is $108,800 to $147,200.
#J-18808-Ljbffr