המקום בו המומחים והחברות הטובות ביותר נפגשים
Your responsibilities will include:
Managing projects for sustaining and new production equipment, process improvements, cost reduction initiatives, and new product onboarding
Collaborating with SFMD suppliers on current products and new product development activities including process development, validation, capacity analysis and capability studies; conduct process risk reviews
Reviewing and managing supplier change requests through the Supplier Change Impact Assessment (SCIA); drive change notice and approval processes
Troubleshooting issues related to the designs, materials or processes of new and existing products
Analyzing test results to provide summarized reports and documentation on findings; make recommendations to the technical teams and leadership
Leading and collaborating with cross-functional teams such as R&D and process development to ensure project success; support value improvement projects (VIP)
Qualification activities through the design and coordination of engineering tests and experiments including DOE; review and provide feedback on SFMD supplier IQ/OQ/PQ, test method validations, and PFMEA
Providing onsite training and guidance to SFMD supplier operators and technicians as needed
Required qualifications:
Bachelor's Degree in any engineering discipline; electrical engineering is preferred
5+ years of working within manufacturing and/or process development
Experience working in medical device or similarly regulated industry
Strong technical acumen and decision-making skills; ability to solve problems and implement solutions
Experience leading and influencing internal and external teams to drive results
Ability to work independently and collaborate with cross-functional teams to complete projects and tasks
Able to travel 25-30% - domestic and international
Preferred qualifications:
Experience with Supply Chain and/or Supplier Relationship Management
Strong interpersonal skills with ability to communicate effectively with individuals on all levels
Strong Good Documentation Practice experience
Detail-oriented with strong organizational skills; ability to multi-task and manage competing priorities effectively
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
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