Boston Scientific is looking for a Quality Engineer II to implement manufacturing process controls and ensure quality assurance requirements are met to support divisional and corporate quality initiatives, goals, and objectives within a manufacturing environment.
Requirements
- 2+ years working in the Medical Device industry (or similar field) in a role directly supporting a manufacturing or production
- Experience in Lean, Six Sigma, Process Improvement, Root Cause Analysis, Critical Thinking/Problem-solving skills
- Exposure to packaging and final pack requirements
- Exposure to localization requirements
Responsibilities
- Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements.
- Acts as an effective team contributor in supporting quality disciplines, decisions, and practices.
- Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
- Assure in the development and execution of consistent and streamlined business systems which effectively identify and resolve quality issues.
- Collaborate cross functionally with local and divisional team members on assigned projects to ensure quality compliance
- Effectively contribute, evaluate, review and approve project plans, risk management files and process verifications
- Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
Other
- Bachelor’s degree in engineering, technology, life science, or related discipline
- Excellent interpersonal and relationship building skills
- Ability to travel up to 10%
- Proven ability to influence without authority
- Attention to detail
