Contract though end of 2025
Pay $45 an hour
We are looking for a Quality Engineer 1 to join our team. In this role, you'll be responsible for developing and maintaining quality processes and inspection methods, including gauging, programming, and documentation. You will work closely with Quality Control, Product Development, and Manufacturing Operations to support daily production and site initiatives. A key part of your role will be ensuring our quality system remains compliant with both internal and external medical device industry standards and regulations.
We need a proactive individual who is eager to learn, has a solid understanding of manufacturing and quality principles, and possesses great communication skills. You should also be technically proficient with common software like Word and Excel and have a keen eye for detail. Experience with statistical analysis, software development, and familiarity with Tulip, Jira, and Agile methodology is highly preferred.
Competencies
- Communication: Must be able to communicate effectively, both verbally and in writing.
- Project Management: Effective project and time management skills; able to work independently and within a cross-functional team.
- Technical Skills: Proficiency with PC applications, including Microsoft Word, Minitab, PowerPoint, MS Project, Visio, and Excel.
- Collaboration: Frequent interaction with peers, management, production associates, and external suppliers.
salary: $44 - $45 per hour
shift: First
work hours: 8 AM - 9 PM
education: Associate
Responsibilities
Key Responsibilities
- Design and Development: Create and implement various inspection techniques and procedures to ensure product integrity.
- Documentation and Procedures: Write, approve, and implement inspection procedures for all stages of production (Receiving, Floor, Final) and support operator self-inspection.
- Gauging and Tools: Work with other Quality Engineers and Metrology Lab personnel to develop and procure product gauging, optical comparator overlays, and templates.
- Process Improvement: Coordinate and execute the development of quality processes, including work instructions, procedures, and test methods.
- Training: Train Manufacturing Associates on measuring, testing, and inspection techniques.
- Analysis and Validation: Perform first article inspections, capability studies, process validations, and metallurgical analyses as needed.
- Problem Resolution: Collaborate with suppliers, engineers, and manufacturing associates to resolve quality issues by compiling and analyzing data, and presenting feedback to internal and external vendors.
- Education: Bachelor’s degree in Biomedical, Mechanical, Electrical, or a related Engineering or Technical discipline.
- Experience: 0–2 years of experience in a technical or manufacturing role is preferred.
- Certifications: ASQ CQE or Six Sigma Green Belt certification is a plus.
Skills
Qualifications
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Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.