Location: Mounds View, MN Duration: 6+ months (possibility of extension) POSITION DESCRIPTION: This is a six-month role, with potential to extend, for an experienced communicator who can provide broad program support for a large, global transformation effort within the Supply Chain organization. We are looking for someone who can commit to 30-40 hours/week, helping develop [...]

Location: St. Paul, MN Duration: 4+ months POSITION DESCRIPTION: The Product Security Technical Writer is responsible for gathering and editing technical information into clear and concise documentation for both technical and non-technical audience that may include R&D, Quality, Regulatory, IT, and other operational teams.  Responsibilities will include documentation management, review, and maintenance. POSITION RESPONSIBILITIES: Write [...]

Location: Arden Hills, MN Duration: 12+ months POSITION DESCRIPTION: You will work collaboratively with development teams to create customer-facing manuals and labels necessary to support the client’s worldwide regulatory, marketing, and sales objectives. By joining their Technical Communications team, your work will be a part of the life-saving products used around the world. POSITION RESPONSIBILITIES: [...]

Location: St. Paul suburbs, MN Duration: 12+ months (potential contract to hire) POSITION DESCRIPTION: Working without appreciable direction, acts as the lead writer for the development of large technical publications projects.  Recommends, interprets and implements company policies and procedures to accomplish assignments and resolves a broad range of complex issues and problems. Identifies and routinely [...]

Location: Maple Grove, MN Duration: 6-12 months (w/possibility of extension or full time hire) Position Responsibilities Responsible for coordination of all product labeling deliverables (will vary by project), including labels, IFUs/DFUs, and carton and pouch artwork, patient labeling, etc. Manage and coordinate creation/revision of deliverables from project initiation through completion. Assess the scope of each [...]

Location: Plymouth, MN Duration: 6+ months Position Responsibilities Regulatory MDR specialist to help facilitate remediation for Class I devices - Complete MDR-compliant STEDs, DoCs, etc. Help cross-functional team assess gaps, develop and execute to plans for remediation Review/approve relevant DHF documentation, including risk analyses, test protocols and reports, clinical evaluation reports, postmarket surveillance plans, etc. [...]

Location: St. Paul, MN Duration: 6+ months Position Responsibilities Under the direction of the Clinical Evaluation Report Project Manager (CER PM) and Director, will be asked to perform the following: Author, review, quality control, and/or provide feedback, in accordance with client processes and procedures, documents related to clinical evaluation of medical device products including: Clinical [...]

Location: Plymouth, MN Duration: 6+ months Position Responsibilities Responsible for developing and maintaining label content for new and existing medical device products. Creates & modifies product labeling, packaging artwork and other related materials incorporating regulatory requirements and branding guidelines. Works with external customers to manage labeling developed for or at external suppliers. Collaborates with cross [...]

Location: Minneapolis, MN Duration: Temp-to-Hire Job Purpose Design, develop and write technical materials for products, such as equipment manuals, product support materials, and operating & maintenance instructions in accordance with company engineering standards.  This documentation will be used in the sale, operation, training and repair of products. Essential Duties Initiate and produce clear, concise, and [...]