Quality Engineer II at Boston Scientific Corporation Malaysia

Arden Hills, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

27 Jan, 26

Salary

0.0

Posted On

29 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Engineering, Manufacturing Engineering, Problem Solving, Statistical Analysis, Analytical Skills, Process Control, Continuous Improvement, Documentation Practices, Communication Skills, Project Management, Risk Management, Supplier Quality, CAPA, Medical Device Experience, Microsoft Office, Manufacturing Control Software

Industry

Medical Equipment Manufacturing

Description

Partners with Manufacturing Engineering and Production core team members for daily manufacturing line support decisions and practices. Collaborates with cross-functional team to evaluate manufacturing results, assist defect detection, primary cause identification, and understanding corrective and preventative actions. Identifies and implements effective process control systems to support the development, qualification, validation and verification to meet or exceed internal, external, and regulatory requirements. Supports a culture of continuous improvement by advancing improvements to existing processes and controls. Proactively investigates, identifies, and implements best-in-class Quality Engineering practices. Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Broadly engages with production teams across all shifts to develop and support solutions to improve outgoing quality. Provide task direction, coaching, and mentorship for technician team members. Participate in team decision-making and display team problem-solving/communication skills. Bachelor's degree in engineering, technology, mathematics, or related science 2+ years of relevant experience in a regulated industry Strong verbal and written communications skills; Good documentation practices Works effectively in a Controlled Environment Area (CEA) manufacturing environment Self-starter with a proven ability to successfully work with minimal supervision Knowledge of basic Quality Management Systems Proficient with Microsoft Office tools (Word, Excel, PowerPoint, Outlook) Medical device experience Comfortable with utilizing analytical equipment (including microscopes) Strong analytical skills, problem solving, and statistical analysis (Excel, Minitab) Experience with the following disciplines: manufacturing/process engineering, post-market complaints, supplier quality, CAPA, risk management Experience running/owning nonconforming event risk assessments and investigations Proficient using manufacturing control software (various MES, MasterControl, etc.) Project management experience

Responsibilities

The Quality Engineer II partners with Manufacturing Engineering and Production teams to support daily manufacturing line decisions and practices. They collaborate with cross-functional teams to evaluate manufacturing results, assist in defect detection, and implement effective process control systems.