R&D Senior Mechanical Engineer

FloodGate Medical•Tampa, FL

15d

About The Position

R&D Senior Mechanical Engineer Cytrellis Cytrellis is a Massachusetts-based medical technology company pioneering new approaches in aesthetic medicine. Their flagship product, ellacor, uses proprietary “Micro-Coring®” technology to remove micro-cores of skin tissue offering a first-of-its-kind, minimally invasive, in-office option to reduce sagging skin and treat moderate to severe wrinkles without surgery, thermal energy, or scarring. Most recently, Cytrellis released ellacor 2.0, improving procedure speed, consistency, and patient healing times, a move that reinforces their mission to expand access to safe, effective, and innovative skin-rejuvenation treatments.. Why You Should Join Us This is an R&D Senior Mechanical Engineer role in Boston, MA . As a Senior Mechanical Engineer, you will be responsible for the design, development, and implementation of mechanical systems and components for medical devices in compliance with regulatory standards.

Requirements

Bachelor’s degree in Mechanical Engineering; Master’s degree preferred.
5+ years of experience in mechanical engineering, with 3+ years of experience in the medical device industry.
Proven track record of successfully leading and managing cross-functional engineering teams in the development of medical devices.
Strong understanding of mechanical design principles, materials selection, and manufacturing processes relevant to medical devices.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal teams and external partners.
Experience with solid modeling (SolidWorks), engineering drawings, GD&T, and design for manufacturability and assembly (DFMA).
Demonstrated leadership skills with a focus on driving results, fostering innovation, and developing talent within the team.

Nice To Haves

Master’s degree preferred.

Responsibilities

Work with engineers across disciplines in the design and development of medical devices from concept to production.
Drive innovation and continuous improvement in system design processes and methodologies.
Collaborate closely with cross-functional teams including R&D, product management, quality assurance, and regulatory affairs to ensure successful product development.
Establish and maintain design control processes to ensure compliance with regulatory requirements such as FDA, CE, and ISO.
Provide technical guidance and mentorship to peers, fostering a culture of excellence and accountability.
Participate in risk management activities and provide input on design mitigations to ensure product safety and efficacy.
Manage project timelines, budgets, and resources to meet product development goals.
Stay current with industry trends, emerging technologies, and regulatory changes related to medical devices and mechanical engineering.