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Mechanical Engineer

1 month ago

Edison, New Jersey, United States Actalent Full time
Job Title: Mechanical Engineer

Job Summary:

We are seeking a highly skilled Mechanical Engineer to join our team at Actalent. As a Mechanical Engineer, you will be responsible for supporting product development, quality assurance, and project management activities. You will work closely with cross-functional teams to design, develop, and implement new products and processes.

Key Responsibilities:

  • Support feasibility analysis for FDA requirements and execute implementation plans as appropriate.
  • Manage and support production and product conversion, including the production of Medical and Life Science products.
  • Prepare bills of materials, drawings, and process support for new designs and product improvement ECNs.
  • Locally responsible for the development and implementation of testing labs/calibration activities in line with strategic plans.
  • Assist Sales with customer questions as part of the technical resource team.
  • Participate in product development and creation of new products or customer solutions.
  • Support developing Master Project Plan and keep track of key milestones of FSI Product Development activities.
  • Support the development of fabricated parts design and assembly instructions for manufacturing.
  • Assist with agency inspections on plant visits (FDA, UL, ETL, CSA, NSF).
  • Lead Product Care activities for Accucold and Summit, supporting FSI field problems technical resolution.
  • Monitor Quality KPI results trends, tracking and evaluating the results, defining action plans when appropriate for securing predictability of results and promptly reporting deviations and corresponding corrective actions.
  • Interface with Product Development, Engineering, Purchasing, and Logistics organizations to provide expert quality guidance.
  • Liaison and interface with suppliers in problem-solving and product development activities.
  • Support the development of a culture of quality, prevention, definition of work standards, quality criteria, and key performance indicators implementation.

Requirements:

  • Feasibility analysis for FDA requirements
  • Product conversion and production support
  • Preparing bills of materials and drawings
  • Testing labs development and calibration activities
  • Project management
  • Fabricated parts design
  • Agency inspection assistance (FDA, UL, ETL, CSA, NSF)
  • Quality KPI monitoring and evaluation

Work Environment:

This is a fully on-site position in Edison, New Jersey. Travel to the Bronx 1X per week is required, with flexible arrival times. Future travel to the Freehold site will be needed as activity increases.

About Actalent:

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation, and speed to market.

Diversity, Equity & Inclusion:

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. We maintain an inclusive environment through persistent self-reflection, build a culture of care, engagement, and recognition with clear outcomes, and ensure growth opportunities for our people.

Equal Opportunity Employer:

Actalent is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information, or any characteristic protected by law.