Our mid-sized contract manufacturing client is adding a Design Engineer to plan and develop robust designs per customer specifications. They work with some of the largest medical device manufacturers, defense contractors, and other large growing industrial companies. Their high-tech equipment is the backbone of precision manufacturing. CNC machining stations with 3-axis, 4-axis, and 5-axis capabilities enable them to perform multi-dimensional machining with unparalleled accuracy and efficiency.   Your role with the company: Work with customers

Our mid-sized contract manufacturing client seeks a Mold Build Supervisor for the first shift to support their manufacturing facility. The Mold Build Supervisor will oversee shop employees in a manufacturing and assembly environment. This role involves planning and assigning work, implementing policies and procedures, and recommending improvements in production methods, equipment, operating procedures, and working conditions. Additionally, the supervisor will be responsible for purchasing materials and scheduling jobs that are being produced.   Your role with the company: 5S + Safety

Our mid-sized cardiovascular medical device client is seeking a permanent Principal Systems Test Engineer to join their team. This is a key technical leadership role responsible for leading the development and execution of comprehensive testing strategies. Responsible for evaluating, developing, and implementing test systems/tools/equipment, including design documentation. The position will provide Verification and Validation expertise to new product introduction of electro-mechanical, software-controlled medical devices. This role requires a deep understanding of medical device systems, strong leadership abilities

Our small start-up client is adding a scientific minded Clinical Data Manager to join their team. In this role, you will oversee the data management aspects of clinical trials from beginning to end. Your main focus will be on ensuring data integrity, quality, and compliance with clinical trial requirements. This position requires a strong understanding of cardiovascular knowledge, proficiency in clinical data management processes, excellent project management skills, and the ability to collaborate effectively with cross-functional teams. If

Our mid-sized medical device client is adding a Sr. Clinical Research Associate to the team. The Sr. CRA is responsible for initiating and overseeing clinical centers to ensure the successful conduct of active clinical studies. The Sr. Clinical Research Associate will ensure that clinical centers perform the clinical study according to the study protocol and regulatory standards by qualifying, training, monitoring, and overseeing study conduct at multiple clinical centers. Your role with the company: Identify and assess the suitability

Our mid-sized medical device client is adding a Clinical Study Manager to the team! The Clinical Study Manager will report to the Sr. Clinical Manager and oversee clinical activities related to one or more clinical studies, and performing/managing the daily in-house operations associated with the studies. The Clinical Study Manager will work independently on multiple complex clinical studies using critical thinking skills. Will be managing one study in start-up and another ongoing study. The new study will

Our mid-sized medical device client is looking for a seasoned engineer. The Product Development Engineer III with a mechanical focus, is responsible for development and implementation of new products, developed jointly with Process Development and Manufacturing Engineering, into full production, as well as supporting of continuation engineering on existing product lines. The role will be about 70% Project Management with about 30% technical. Your role with the company: Product Concept: *Basic understanding of customer/user and patient needs. *Proposes concepts

Our mid-sized medical device client is adding a Sr. Design Assurance Engineer to the team! The Sr. Design Assurance Engineer utilizes risk management and quality planning activities to provide quality engineering support of product/process development and input to Quality Management Systems affecting product/process development. Champions departmental or cross-functional engineering initiatives and acts as an effective leader or team member in supporting quality disciplines, decisions and practices. Your role with the company: Key member of medical device development project

Our small start-up client is adding (Sr.) Clinical Research Associates (CRA) to the team. The CRA works as part of the clinical team to ensure the completion of company-sponsored clinical studies.  As an internal and externally facing position, this position interacts directly with the internal study team, clinical vendors, clinical Investigators, and other study staff at a clinical research site.  The CRA will be the primary contact for the study sites regarding the proper execution of the clinical

Our small, well-funded start-up client is adding a Clinical Project Manager to the team.  The Clinical Project Manager will report to the VP Clinical (lives in MN) and will be a remote role with minimal travel. The Clinical Project Manager leads the planning, development and execution of the clinical research trial(s). Ensures compliance to study protocol, Good Clinical Practices, applicable domestic and international regulatory standards, and Standard Operating Procedures. The Clinical Project Manager will participate in development

Our mid-sized medical client is adding a Sr. Regulatory Affairs Specialist to their team! The Sr. Regulatory Specialist will support international registrations and renewals. This individual is responsible for ensuring product approvals are properly maintained, and product re-registrations are properly managed.  The Sr. Regulatory Affairs Specialist will perform regulatory submission/approval activities for all products and ensures compliance with required regulations and established corporate standards. Your role with the company: Preparing documentation for international regulatory registrations Preparing technical documentation

Our smaller medical device client is adding a Director of Electrical and Software Engineering to lead an engineering team in creating groundbreaking solutions. The Director of Electrical and Software Engineering will play a pivotal role in driving the development and implementation of electrical and software systems for innovative medical devices. This leadership position requires a seasoned professional with a proven track record in both electrical and software engineering, as well as a deep understanding of regulatory requirements within the medical

Our mid-sized medical device client is adding a Senior Quality Engineer to the team! The Sr. QE will have the opportunity to be a key team member in supporting a medical device from transfer to manufacturing through commercial distribution. They are responsible for ensuring a smooth transition of new products to the manufacturing floor with the assistance of a cross-functional team. They will maintain oversight of all manufacturing activities and be responsible for the final release of sterile