RQM+ is the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clinical trial, lab and reimbursement services – reducing risk and supporting market access throughout the entire product lifecycle for medical devices, digital therapeutics and diagnostics. With more former FDA, Medicines and Healthcare Products Regulatory Agency (MHRA) and notified body regulators than any other firm, the RQM+ team has deep expertise in all clinical specialties. RQM+ currently works for 19 of the top 20 medical device manufacturers and seven of the top 10 IVD companies.
The Labeling Project Specialist (LPS) plans, manages, and directs the creation/revision of product literature and labeling. The LPS works closely with project teams to ensure labeling content is developed per, and compliant to, all applicable procedures. They develop schedules and ensure labeling deliverables are executed to them while maintaining a high standard of quality. The LPS is the resident expert and primary point of contact for all things related to product literature and labeling.
12 Month Contract
Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!
We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.
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Are you ready to take your career to the next level as a Labeling Project Specialist Contractor with RQM+ in Minneapolis, MN? As the leading MedTech service provider, RQM+ is committed to delivering top-notch regulatory and quality expertise for medical devices, digital therapeutics, and diagnostics. In this vital role, you'll be at the heart of product literature and labeling initiatives, ensuring compliance while managing schedules and deliverables with precision. Your responsibilities will include coordinating all product labeling materials, such as labels and instructions for use, while keeping quality as your number one priority. You'll harness your experience in regulated industries to liaise with project teams and help guide them towards successful outcomes. If you're passionate about improving content consistency and facilitating cross-functional collaboration, this is the place for you. At RQM+, we value continuous improvement, innovative ideas, and creating a stellar work environment where every employee is considered part of our family. With a strong emphasis on professional development and work-life balance, this 12-month contract role allows you to make a significant impact in a rapidly evolving field. Join us in shaping the future of healthcare while advancing your career with a company that truly cares about its people. If you're ready to embrace the challenge and enjoy the perks of being a part of RQM+, we encourage you to apply today and learn more about the journey ahead!
RQM+ is the leading MedTech service provider with the world’s largest global team of regulatory and quality experts. Building upon 40 years of regulatory expertise, we also provide comprehensive clinical trial, lab and reimbursement services – red...
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