Scientific Search
Overview
Senior Quality Engineer
— Racine, WI (Hybrid). Are you ready to play a pivotal role in ensuring the quality and safety of life-changing medical devices? Our client is looking for a driven
Quality Engineer
or
Senior Quality Engineer
to join their team. You’ll work across departments, from R&D to operations, ensuring compliance with regulatory standards and improving processes that directly impact the healthcare industry. Join a family-owned company committed to improving lives around the world through cutting-edge medical innovations! Why You Should Apply
Work with innovative products that improve global healthcare. Opportunity to lead quality improvement initiatives across various departments. Comprehensive benefits, including medical, dental, vision, and 401(k) from day one. Generous paid time off (20 days) and 15 paid holidays. Paid parental leave and employee bonuses. Amazing Salary and Benefit Package. Responsibilities
Leading or supporting change control, NCR, CAPA, and quality surveillance activities. Conducting risk management and design control processes for product changes and new product launches. Engaging in internal and external audits, ensuring compliance with regulatory bodies. Driving quality improvement initiatives to enhance efficiency and reduce defects. Managing adherence to regulatory standards, including ISO 13485 and FDA Quality System Regulations. Qualifications
Bachelor’s degree in Physical Science, Engineering, or equivalent experience. Strong knowledge of FDA regulations, ISO 13485, and risk management (ISO 14971). Expertise in NCR/CAPA processes and electromechanical device validation. Proficient in software integration and auditing, with excellent communication skills. How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to emily@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#18914.
#J-18808-Ljbffr
Senior Quality Engineer
— Racine, WI (Hybrid). Are you ready to play a pivotal role in ensuring the quality and safety of life-changing medical devices? Our client is looking for a driven
Quality Engineer
or
Senior Quality Engineer
to join their team. You’ll work across departments, from R&D to operations, ensuring compliance with regulatory standards and improving processes that directly impact the healthcare industry. Join a family-owned company committed to improving lives around the world through cutting-edge medical innovations! Why You Should Apply
Work with innovative products that improve global healthcare. Opportunity to lead quality improvement initiatives across various departments. Comprehensive benefits, including medical, dental, vision, and 401(k) from day one. Generous paid time off (20 days) and 15 paid holidays. Paid parental leave and employee bonuses. Amazing Salary and Benefit Package. Responsibilities
Leading or supporting change control, NCR, CAPA, and quality surveillance activities. Conducting risk management and design control processes for product changes and new product launches. Engaging in internal and external audits, ensuring compliance with regulatory bodies. Driving quality improvement initiatives to enhance efficiency and reduce defects. Managing adherence to regulatory standards, including ISO 13485 and FDA Quality System Regulations. Qualifications
Bachelor’s degree in Physical Science, Engineering, or equivalent experience. Strong knowledge of FDA regulations, ISO 13485, and risk management (ISO 14971). Expertise in NCR/CAPA processes and electromechanical device validation. Proficient in software integration and auditing, with excellent communication skills. How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to emily@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job#18914.
#J-18808-Ljbffr