Electromechanical (EM) Manufacturing Engineer - Boston

FloodGate Medical•Tampa, FL

19d•Onsite

About The Position

Electromechanical (EM) Manufacturing 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 Electromechanical (EM) Manufacturing Engineer role in Woburn, MA . The Electro-mechanical Manufacturing Engineer is responsible for evaluating and refining current manufacturing processes and working with our Contract Manufacturers to establish best practices. The Electro-Mechanical Manufacturing Engineer will be involved in the continued refinement of our production process to ensure that products can be manufactured to specifications. The position may be required to perform all, or a combination of the following essential responsibilities as determined by necessity. This role is located at the Company’s Woburn, MA office.

Requirements

Bachelor's degree in Manufacturing Engineering, Mechanical or Electrical Engineering, or Industrial Engineering, or equivalent job experience
5+ years of related engineering experience, preferably in new product development environment.
Proficiency in designing and developing manufacturing processes, work instructions, and test fixtures.
Familiarity with Lean Manufacturing and/or Six-Sigma Principles.
Familiarity with SPC and Statistical Sampling techniques.
Excellent interpersonal and presentation skills, with the ability to clearly present recommendations and ideas and to summarize complex issues.
Ability to work well under pressure in a fast-paced, time-sensitive environment with shifting priorities and multiple deadlines.
Proven problem-solving capabilities and strong analytical skills.

Nice To Haves

Medical device experience desired.
Experience using statistical analysis software is a plus.
Experience in metrology techniques is a plus.
Experience working with a variety of manufacturing and prototyping methods.

Responsibilities

Develop and implement manufacturing processes to ensure products are manufactured to the required specifications and standards. This includes creating work instructions, assembly procedures, and fixturing for the manufacturing process.
Work within the Engineering team to drive design for manufacturing and assembly early in the design process for new product development.
Evaluate and troubleshoot electromechanical systems including boards, communications, mechanical, simple vacuum system and handpieces issues.
Manage the manufacturing process to ensure that the products are manufactured to the required specifications and timelines. This includes monitoring the manufacturing process, identifying and resolving issues, and ensuring that the products meet the required quality standards.
Ensure that the manufacturing process and products comply with all relevant regulations, standards, and guidelines. This includes working with regulatory agencies to obtain necessary approvals and certifications.
Collaborate with cross-functional teams, including product development, quality assurance, supply chain, and logistics, to ensure the successful manufacturing and delivery of products.
Continuously improve manufacturing processes to optimize efficiency, reduce costs, and improve quality. This includes identifying opportunities for improvement and implementing process changes.
Conduct supplier audits to ensure that the third-party manufacturers are complying with the required standards and regulations. This includes conducting on-site visits and assessments of the manufacturers' quality systems and assessments of the manufacturers' quality systems and processes.
Manage relationships with third-party manufacturers to ensure that they are meeting the required performance standards. This includes communicating performance expectations, addressing performance issues, and negotiating contracts and pricing
Contribute to FMEAs and risk documentation as a technical subject matter expert.