Luxury Lake Minnetonka living at its finest, where every season brings a new dimension of beauty, relaxation and adventure to your doorstep.
Nestled on nearly 2 acres of private woods, this estate offers an unrivaled lifestyle experience. As you step into this Sharratt & Co designed home prepare to be "wowed" with floor to ceiling windows that
This home is under construction and estimated to be complete March of 2024 Photos are for illustration purposes only.
Our new Madison Plan has a covered entry welcoming you into the foyer space with closet. The open layout has a well appointed kitchen with white cabinets, granite countertops, stainless GE appliances, luxury vinyl plank floors
surgery markets. PMT Corporation provides future opportunities in sales, marketing and management. POSITION The Quality and Regulatory Department support the registration and compliance of PMT’s products in the US and for over 100 distributors worldwide, selling specific PMT products.
The Regulatory Affairs Specialist will focus on assisting PMT maintain product compliance with FDA/MDSAP, ISO, and MDD/MDR requirements. This is a salary position and is an in-office position where the candidate will be working at PMT headquarters in Chanhassen, MN 8:00am – 4:30pm, M-F. DUTIES backss regulatory requirements and develop procedures and strategies for maintaining compliance. Maintenance of
FDA/MDSAP, ISO, and MDD/MDR compliance. Work with Engineering and Quality departments in product development to ensure compliance throughout design and manufacturing processes.
Review Engineering Change Orders relating to design, engineering, or manufacturing. Work directly with internal auditors and quality managers on compliance related matters. Maintain good relationship and interact directly with external auditors and regulatory agencies at the reviewer level. Interact with regulatory departments for international distributors to assist in registrations and license and certificate renewals. Provide support and leadership on development projects and regulatory issues to ensure timely
submissions for market clearance. Prepare US and international submissions for new products or products with changes in a timely manner.
REQUIREMENTS Bachelor’s degree in science, regulatory affairs, engineering, or other related field. Strong attention to detail. Minimum 2 years’ experience in regulatory affairs in health sciences, preferably medical devices. Regulatory Submission experience with 510Ks, notified bodies, or international MOH agencies. Knowledge of regulatory process for US and EU, experience in other countries a plus. Strong work ethic able to consistently exceed expectations. Excellent communication and time management skills. Proficient in Microsoft Office Suite and Adobe. PMT is an Equal Opportunity Employment
Our community of spacious one, two and three bedroom apartment homes feature modern oak cabinetry, energy efficient appliances, in-home washer and dryer and heated underground parking.
Gateway Place is conveniently located off Highway 212 and Great Plains Blvd and close to Lake Susan Park, Chanhassen Target, two grocery stores and plenty of
Step into the ultimate entertainer's haven - a seamlessly updated & luxurious open-concept 1 level lake home.
From the sophisticated interior to the expansive, maintenance-free decking spanning the entire back of the house, this residence invites you to effortlessly transition between indoor and outdoor living. The spacious backyard beckons
