Quality Engineer II

Cirtec Services GmbH; Brooklyn Park (MN); On-site; USD 80,000 - 95,000; Full time

Benefits offered by this job

Healthcare & Wellness

Training & Career Development

401(k) with company match

PTO

Job summary

Cirtec Medical Corporation is seeking a Quality Engineer to monitor and audit manufactured goods in a medical device setting. You will identify defects, determine causes, and implement corrective actions while collaborating with customers and suppliers on engineering projects.

Responsibilities include quality engineering support across development and manufacturing, CAPA ownership, validation protocol development, and process improvements to drive compliance and product quality.

Qualifications

• Bachelor's degree in a STEM field is required.
• Minimum of 2 years' engineering experience in a related field.
• Experience with medical devices or regulated environments is preferred.
• Strong data analysis and quality improvement mindset.
• Proficiency with Microsoft Office applications.

Responsibilities

• Provide Quality Engineering support for development or manufacturing.
• Lead CAPA investigations and issue resolution with root-cause analysis.
• Develop and manage validation plans and SOPs.
• Support product transfers from validation to production.
• Coordinate with customers and suppliers on quality-related matters.
• Implement continuous improvement initiatives for processes.
• Review changes to procedures to ensure quality system compliance.

Skills

Quality Engineering

CAPA Management

DOE & Stats

Validation

Process Improvement

Data Analysis

MS Office

English Proficiency

Education

Bachelor's degree in STEM field

Tools

Microsoft Word

Excel

PowerPoint

Access

Job description

Description

About us:

For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems.

Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team!

Position Summary:

This position is primarily responsible for monitoring and auditing the quality of all manufactured goods in a medical device industry. Will work to not only find defects, but also to find the cause of the defect and develop a solution. Interacts with customers and suppliers in support of engineering projects.

Key Responsibilities:

• Provide Quality Engineering support for engineering project development, or sustained manufacturing.
• Provide Quality Project Management support as needed for product transfers from development to validation.
• Validation System Owner responsible for the development and management of the validation master plan along with the validation determination.
• Develop and maintain Validation Standard Operating Procedures.
• Develop and maintain project Quality Plan for assigned projects.
• Develop protocols, perform statistical analyses, and write reports for validations and formal process development, which requires quality-engineering involvement such as DOEs.
• Support the development and implementation of IQ (Installation Qualification) and OQ (Operational Qualification) protocols to ensure compliance with the Quality System.
• Provide Quality Engineering support for manufacturing.
• CAPA (Corrective and Preventative Action) system owner responsible for the support of the corrective action system and procedures.
• Interact with customers and suppliers to resolve CAPA and complaint investigations and in support of manufacturing.
• Provide Quality Support for the disposition of material via NCR's.
• Provide Quality Project Management Support as needed for product transfers from validation to production.
• Vendor approval and maintain and assess vendor performance data (i.e. SCAR/on time).
• Review and document procedure changes for quality requirements and compliance with the quality system.
• Develop quality systems and procedures as needed.
• Audit support for third party audits, customer audits and internal audits.
• Support the implementation of continuous improvement initiatives for production processes.
• Develop and maintain production quality control plans.
• Initiate and maintain SPC (Statistical Process Control) for production processes.
• Provide initiative and support for FMECA (Failure Modes & Effects Criticality Analysis), and DOE (Design of Experiment as applicable.
• Comply with all work rules including those pertaining to safety, health, quality and Cirtec policies.
• Back up to Quality Systems Administrator.
• Complies with company, quality and safety standards, policies, and procedures

Must Have:

• Bachelor's degree in a STEM related field, required
• Minimum of 2 years' engineering related experience
• Experience in an engineering environment with mechanical, tool design, and manufacturing processes (medical device preferred)
• Analyze and process Information, Promote Process Improvement, Developing Standards, Managing Processes, Manufacturing Methods and Procedures, Supports Innovation.
• Must be fluent in use of computer systems for the analysis of data, specifically Microsoft Office.
• Must possess excellent verbal communication, organizational and management skills.
• Training or equivalent experience in computer use and software-Microsoft Word, Excel, Power Point and Access.
• Must be able to read, write and speak fluent English.
• Must be able to implement quality programs, interpret the collected data, and present the data to management to drive continuous improvement.

Good to have:

• Previous Medical Device Experience

Salary Range:

Competitive market salary from $80000 to 95000 per year depending on qualifications and experience.

Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

Benefits:

We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec's goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

• Training and career development
• Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs
• Paid Time Off and 401(k) retirement savings with a company match.