Intellectt Inc

Manufacturing Engineer (medical device)

Intellectt Inc Westbrook, ME
Intellectt Inc

Manufacturing Engineer (medical device)

Intellectt Inc Westbrook, ME
3 months ago 41 applicants

See who Intellectt Inc has hired for this role

Hello,

Hope you are doing well.

This is Jahera and I'm a recruiter at Intellectt, Inc. Please find the job description and reach out to me with an updated copy of your resume. You can send it to jahera@intellectt.com or call me at +1(732) 276-1791

Role: Manufacturing Engineer II

Location: Westbrook, ME - 04092

Duration: 5 Months

Shift Timings: 8am - 5pm

Responsibilities

Job Description:

  • Develop, implement, and optimize manufacturing processes and equipment.
  • Utilize structured problem-solving techniques to identify root causes of failures and implement preventive measures.
  • Troubleshoot equipment by evaluating machine logic, electromechanical systems, and process controls.
  • Conduct design of experiments, validation, testing, and data analysis for continuous improvement initiatives.
  • Recommend and support new methods or materials to enhance quality and efficiency.
  • Assess current equipment for process suitability and develop improvement plans.
  • Prepare and revise manufacturing documents, SOPs, safety instructions, and other technical documents.
  • Collaborate with engineering teams to develop solutions and enhancements.
  • Participate in teams to ensure continual improvement, safety, and compliance.
  • Provide training and expertise for product processing and tooling development.
  • Lead engineering project teams and coordinate activities.
  • Mentor junior engineers and maintenance technicians.
  • Initiate and resolve Quality Incidents and CAPA.
  • Ability to travel up to 25% of the time.

Basic Qualifications | Education:

  • Bachelor's degree (BS) in engineering or equivalent combination of education and experience.
  • Minimum three years of engineering experience in a manufacturing environment.
  • Familiarity with material testing and measuring methods.
  • Proficiency in Database, CAD, Development, Internet, Inventory, Manufacturing, Project Management, Microsoft Excel, and Microsoft Word software.

Preferred Qualifications

  • Experience in GMP, FDA, ISO, and USDA regulated environments.
  • Familiarity with cGMP and ISO 13485 regulations and practices.
  • Knowledge of statistical analysis software (e.g., Minitab).

  • Seniority level

    Entry level

  • Employment type

    Contract

  • Job function

    Engineering and Information Technology

  • Industries

    Medical Equipment Manufacturing

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