Multi‑Axis CNC Machining Specialist, ISO 13485 - Big Lake, MN
1 day ago

Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
We are currently looking to add a Quality Systems Specialist to our Quality Assurance team in St. Cloud, MN.This role is hands-on and detail-oriented... · ...
1 month ago
This role involves preparing regulatory submissions for new products changes renewals to support global market access collaborating with cross-functional teams ensuring product documentation aligns with applicable regulatory requirements. · ...
1 month ago
We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. · Support the transition to new site including contractor management, risk identification/mitigation, and the development of site EHS ...
2 weeks ago
We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it's what fuels our motivation and contributes to our success. · ...
2 weeks ago
We are currently looking to add a Quality Systems Specialist to our Quality Assurance team in St. Cloud, MN. · High School education or equivalent required. · Two/Four-year Engineering/Technical or related degree preferred. · ...
1 month ago
Manufacturing Quality Assurance Specialist · Reports to: Quality Manager · About the role · Step into a hands-on quality role where your attention to detail keeps production on spec and customers confident. You'll perform inspections, support PPAP approvals, drive targeted proces ...
1 hour ago
We are seeking a highly experienced contractor to join our Enterprise FCA Execution Team. · This Senior-level role will provide critical support in managing our FCA portfolio, · The ideal candidate will have a robust background in the medical device or pharmaceutical industries,K ...
1 day ago
We are looking for a Document Specialist who will bring a positive mindset and a strong desire to support their colleagues. · ...
1 month ago
+The EHS Specialist II is a member of the EHS team and reports to the EHS Leader. · ...
1 month ago
+Job summary · +This role offers an exciting opportunity to contribute to quality management in the medical device sector, · +Responsibilities<br <+Maintain and update documentation related to Field Corrective Actions (FCA), ensuring compliance and accuracy. · Track open tasks as ...
2 days ago
Collaborate closely with engineers and scientists to develop manage and maintain critical documentation that supports compliance and operational excellence. · ...
3 weeks ago
The Documentation Specialist/Technical Writer role is responsible for technical documentation. · In this role, individuals will use engineering CAD data to develop and maintain installation, · maintenance and product specification documents. ...
1 week ago
As a Laboratory Compliance Specialist you will support our internal materials characterization laboratory by ensuring the integrity and compliance of data documentation and testing interpretations. · ...
4 weeks ago
+Job Summary · Looking Laboratory Compliance Specialist to support internal materials characterization laboratory by ensuring data integrity and compliance. · +Conduct peer reviews of analytical test data. · Validate data for regulatory submissions. · Recommend process improvemen ...
3 weeks ago
We're seeking a Senior Quality Specialist to support and maintain our Quality Management System and ensure compliance with FDA and international regulatory requirements.Transcend, Inc. is a fast-growing, Twin Cities-based medical device company transforming the way people experie ...
1 day ago
Are you detail-oriented, organized, and passionate about creating and maintaining high-quality technical documentation? · ...
4 weeks ago
We are seeking an enthusiastic Associate Compliance Specialist to join our team. This role offers an exciting opportunity to contribute to quality management in the medical device sector, supporting essential documentation and task tracking. · ...
2 days ago
The Regulatory Compliance Specialist will play a critical role in supporting internal materials characterization laboratory integrity and compliance by ensuring data accuracy. · Partner with R&D engineers and scientists for high-quality analytical testing. · Conduct peer reviews ...
3 weeks ago
You'll collaborate closely with engineers and scientists to develop, manage, and maintain critical documentation that supports compliance and operational excellence. · ...
3 weeks ago
We are seeking a highly skilled Senior Compliance Specialist to join our team. · ...
1 day ago