Senior Supplier Quality Engineer - Direct Materials Acquisitions

Senior Supplier Quality Engineer - Direct Materials Acquisitions

Work mode:
Hybrid Onsite Location(s):
Arden Hills, MN, US, 55112 Recruiter:
Spencer Gregory Hale Senior Supplier Quality Engineer – Direct Materials Acquisitions Onsite/Hybrid Location(s):
Marlborough, MA;
Minneapolis, MN;

About the role:

The Global Sourcing organization at Boston Scientific is a global, passionate team that oversees a diverse network of suppliers which manufacture finished devices for BSC distribution. The Senior Supplier Quality Engineer will demonstrate a primary commitment to patient safety and collaborate with cross-functional internal/external resources to continually improve our supplier's manufacturing processes. In this role, you will support products within the acquisition space with a primary focus on components.

This position may require a temporary relocation or extended travel assignment to support critical business initiatives. Candidates should be open to a short-term placement that may include approximately 6–9 months in Penang, Malaysia or up to one year in Carlsbad, California, depending on project needs. Flexibility and willingness to travel for these assignments are essential to ensure successful collaboration with global teams and suppliers.

Your responsibilities include:

• Sustaining Engineering:
  Evaluates and communicates quality issues to suppliers and applies sound, systematic problem-solving methodologies in identifying, prioritizing, and resolving quality issues. Reviews and approves supplier corrective action plans and verification of effectiveness documentation. Manages sustaining quality issues, process change impacts, and design change implementations for suppliers within the Acquired Entity Quality system, the hybridized BSC-Acquired Entity Quality System, and in the BSC Quality System after products are successfully integrated.
  
  Proactively assesses supplier capabilities through direct on-site visits and technical discussions. Coordinates the evaluation of proposed changes ns and leads supplier audits to assess compliance with regulatory standards and Boston Scientific requirements, including audit scheduling investigation, and evaluation of audit observation and findings, reporting, follow-up, and confirmation of follow-up actions. Supports Design Quality Assurance with Field Action and Product Inquiry Reports by performing investigations on supplier-related or supplier-caused quality issues.
  
  Investigates complaints and manages NCEPs at OEM suppliers and CM suppliers where the issue is manufacturing-related. Supports Supplier Change Impact Assessments for process changes ports and performs Finished Good Documentation changes in support of ongoing design changes or labeling updates. Leads projects and consistently hits project milestones. Creates crisp and clear project plans and develops strong contingency plans as part of project planning process.
• New Product Development:
  Support manufacturing lines of acquired entity's manufacturing line through integration of acquired company's suppliers and products into BSC's Quality System. Lead the execution of material controls quality deliverables and collaborate with cross-functional new product development teams to onboard suppliers. Generate and review quality plans, agreements, product specifications, component qualifications, design verification/validations, and process validations.
• Quality System Champion:
  Supports Material Controls external regulatory body audits requests as required. Leads or supports Material Controls internal audit efforts. Collaborates with corporate and regional supplier quality organizations on policy, procedure, and guideline development. Includes generation, review, and implementation of these documents. Identifies and advises management on potential improvements to quality systems and processes in the company. Champions 100% compliance to company policies and SOP's.

What we're looking for in you:
Minimal

Qualifications:

BS degree in engineering or technical field with minimum of 5 years of relevant experience. Experience in medical device, automotive, aeronautical, semiconductor, or other regulated industry. Project management: ability to influence cross functional global teams spanning Quality, Operations, R&D, and Sourcing. Experience in process validation, design controls, risk management, CAPA, SCAR. Ability to work independently; organized and self-driven. Articulate communicator; adept at packaging and appropriately scaling information to the intended audience.

Ability to rapidly learn and use new software applications (e.g., PLM, ERP). Domestic and international travel up to 25%.

Preferred Qualifications:

7+ years of medical device engineering experience preferred. Medical Device Industry experience Drug or animal tissue experience Problem Solving and Project Management experience Leadership experience on a materials or service commodity team. Lead auditor of quality systems experience (ISO 13485 or similar). ASQ…