Senior Manufacturing Engineer

Access Vascular•Billerica, MA

About The Position

The Senior Manufacturing Engineer will play a pivotal, hands-on role in developing and optimizing manufacturing processes for cutting-edge, single-use medical devices made from novel biomaterials. This position offers a unique opportunity to contribute to an early-stage, innovation-driven company with strong potential for career growth. The ideal candidate brings deep expertise in process development, project management, and scalable manufacturing, and thrives in a fast-paced environment focused on continuous improvement across processes, facilities, and equipment.

Requirements

  • Bachelor’s degree in Manufacturing, Mechanical, Industrial, or Plastics Engineering.
  • Minimum of 8 years of manufacturing or process engineering experience in a regulated manufacturing environment, preferably FDA/ISO regulated medical device or medical equipment manufacturing.
  • Prior experience leading the design, development, and validation of production processes, fixtures, and tooling.
  • Proven project management experience, with the ability to lead cross-functional initiatives.
  • Proficiency in SolidWorks, including demonstrated expertise in designing fixtures and tooling.
  • Strong organizational skills with the ability to implement and promote structured workflows within engineering teams.
  • Excellent verbal and written communication skills; capable of effectively communicating across all levels and disciplines of the organization.
  • Adaptability to shifting priorities and ability to manage multiple tasks in a fast-paced, dynamic environment.

Nice To Haves

  • Prior work experience leading the development of plastic assembly, hardware assembly, electromechanical assembly and test processes is preferred.
  • Six Sigma Green Belt or Black Belt (preferred).
  • Experience with plastics processing techniques such as extrusion, injection molding, and fiber forming (preferred)

Responsibilities

  • Work hands-on to develop, validate, and implement manufacturing processes to support commercial production and future scalability.
  • Create and maintain process flow diagrams and value stream maps for current and future products.
  • Optimize manufacturing process flow and facility layout to improve safety, quality, efficiency, and accommodate growth and new product introductions.
  • Establish standard work procedures and equipment operating parameters.
  • Write clear, concise work instructions and process documentation to support commercial medical device manufacturing, (including inspection procedures, test protocols, assembly drawings, equipment control documentation, and component drawings).
  • Work with cross functional teams to identify and resolve technical and quality related issues including participation in MRB, customer complaint investigations, CAPA related activities, design activities, and regulatory submissions.
  • Collaborate with Quality Control to resolve supplier quality issues and ensure compliance with regulatory standards.
  • Collaborate with product development teams to design and implement manufacturing tooling and fixtures.
  • Identify, develop, and deploy automation solutions to improve process efficiency.
  • Troubleshoot equipment issues and implement corrective actions.
  • Develop capital equipment proposals to support manufacturing needs.
  • Lead continuous improvement initiatives to reduce manufacturing costs, improve yield, and minimize scrap.
  • Lead cross-functional efforts to streamline production through process improvements, test improvements, and product design changes.
  • Analyze quality issues and implement corrective and preventive actions.
  • Drive operational excellence through data-driven decision-making and lean manufacturing principles.
  • Manage engineering projects from concept through execution, including developing comprehensive project plans and timelines.
  • Present project updates and plans to cross-functional teams and stakeholders.
  • Delegate tasks effectively based on team members’ strengths and experience.
  • Monitor project performance and ensure alignment with short- and long-term organizational goals.
  • Manage project budgets and adjust plans based on financial analysis.
  • Serve as strong team player, supporting and assisting supervisor and colleagues when necessary and complying with all work safety rules and regulations.
  • Provide mentorship and training to junior engineers, technicians, and interns.

Benefits

  • Commensurate With Experience
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