All positions offer opportunity for advancement. If you have the skills and are seeking a challenging growth opportunity, please e-mail your cover letter, resume and salary requirements to hr@rmsmedpro.com or fax to 845-469-5518.

RMS offers a competitive salary and benefits package, including medical, dental, LTD and 401(k).

Regulatory Affairs Associate

06/20/2018 | Chester, NY

Essential Job Functions Collaborate and assist with US and worldwide regulatory strategy regarding class II medical device submissions. Interactions with regulatory bodies with subsequent notifications as needed. Provide support for Company’s Regulatory Affairs and Compliance program. Assist in interpreting and applying FDA regulations to business practices, evaluating risk and proposing solutions to regulatory strategies. Support … Continued

National Accounts Manager

06/19/2018 | Chester, NY

Position Overview The National Accounts Manager is responsible for meeting or exceeding sales revenue, sales profitability and budgetary objectives.  Additionally, this position collaborates with Executive Management on setting sales strategy North America. Essential Job Functions Set direction and manage all sales and business development operations for National Accounts, including pricing, distribution and channel strategy Manage … Continued

Production Assembler

12/21/2017 | Chester, NY

Position Overview The Production Assembler is responsible for meeting production goals, assemble small intricate parts, follow clean room protocol and be a strong team member of the department and company. Essential Job Functions • Product assembly of multiple medical devices that include small intricate parts. Good manual dexterity with frequent use of both hands required … Continued

Clinical and Medical Affairs Associate

08/12/2017 | Chester, NY

Summary Design, plan and conduct clinical research trials (prospective and retrospective for pre- and post-market studies) by executing all relevant activities. Interact with study coordinators and investigators ensuring compliance with study protocols, FDA and international regulations, IRB and/or Ethics Committees requirements in order to achieve overall clinical objectives. Act as Medical Science Liaison (MSL) in … Continued