Sr. Mechanical Engineer
Azenta Life Sciences
Summary
The Mechanical Engineer is responsible for the design/development, modification, and evaluation of primarily mechanical systems, equipment and packages. They may contribute to total systems engineering, including other engineering disciplines and conduct feasibility studies and tests new and modified designs. They are involved in all phases of development from initial concept to manufacturing and may direct support personnel in the preparation of detailed design, design testing and prototype fabrication.
Job description
Job Description
The Mechanical Engineer is responsible for the design/development, modification, and evaluation of primarily mechanical systems, equipment and packages. They may contribute to total systems engineering, including other engineering disciplines and conduct feasibility studies and tests new and modified designs. They are involved in all phases of development from initial concept to manufacturing and may direct support personnel in the preparation of detailed design, design testing and prototype fabrication.
The Mechanical Engineer provides design information to drafting for packaging documentation and, depending on level, may function as a project engineer/leader with the resident responsibilities of proposals/project plan, schedules, work assignments, prime contact, technical presentations, cross functional issue resolution, etc. They are expected to keep up to date on technical advances in the discipline and related fields.
Responsibilities
- Generate concepts, design new product mechanisms, sub-assemblies, and packaging; engineering analysis; generate detailed design and drawings.
- Identify and select vendors, outsource parts and assemblies (off the shelf components, custom items, and fabricated parts)
- Must be hands-on; assemble, troubleshoot, debug, and qualify subsystems and components. Resolve design issues as appropriate.
- Clearly and concisely express and document ideas, options, problems, issues, test results, etc.
- Develop the required documentation during the development and transfer to production (models, detail drawings, diagrams, BOM, assembly procedures, etc.). Generate meticulous, detailed, and thorough documentation.
- Ensure that the specifications, schedule, and budget have been met
- Provide support to manufacturing and field service after product release.
- Work well within the team environment.
Experience
- A Bachelor's degree in Mechanical Engineering required; Master's degree in Mechanical Engineering preferred.
- 5-10 years of design experience, preferably with mechanisms, robotics, or automation.
- A combination of experience and education will be considered.
Position Requirements
- Completed a minimum of 2 product life cycles (from concept to production) as a key contributor.
- Demonstrated capability to perform engineering analysis and familiarity with commonly used analysis tools (e.g., FEM).
- Experience in designing robotics, mechanisms for automation, and complex electro-mechanical products is highly desirable
- Knowledge of machining and fabrication processes for metals and the commonly used plastics.
- Experienced user of SolidWorks CAD or equivalent CAD program
- ISO 13485 and FDA/cGMP experience is a plus.
- Strong organizational skills, detail-oriented while being flexible, open, and able to adapt to changing priorities.
- Must have a strong work ethic and good written and verbal communication skills.
- A self-starter; must be able to work independently with minimum supervision or direction.
Requirements
- Bachelor's degree in Mechanical Engineering required
- Master's degree in Mechanical Engineering preferred
- 5-10 years of design experience, preferably with mechanisms, robotics, or automation
- Completed a minimum of 2 product life cycles (from concept to production) as a key contributor
- Demonstrated capability to perform engineering analysis and familiarity with commonly used analysis tools (e.g., FEM)
- Experience in designing robotics, mechanisms for automation, and complex electro-mechanical products is highly desirable
- Knowledge of machining and fabrication processes for metals and the commonly used plastics
- Experienced user of SolidWorks CAD or equivalent CAD program
- ISO 13485 and FDA/cGMP experience is a plus
- Strong organizational skills, detail-oriented while being flexible, open, and able to adapt to changing priorities
- Must have a strong work ethic and good written and verbal communication skills
- A self-starter; must be able to work independently with minimum supervision or direction
Company overview
Azenta Life Sciences is a leading global provider of comprehensive life sciences solutions dedicated to enabling impactful breakthroughs and therapies to reach the market faster. Headquartered in Burlington, Massachusetts, the company operates worldwide with approximately 3,000 employees across North America, Europe, and Asia. Azenta offers an integrated suite of sample exploration and management solutions that accelerate discovery, development, and delivery processes for pharmaceutical, biotechnology, academic, and healthcare institutions. Their core capabilities span genomics services through GENEWIZ, cryogenic storage systems, laboratory automation, and informatics solutions. The company provides reliable cold-chain sample management, automated storage systems, consumables, instruments, and laboratory information management systems (LIMS) to support drug development, clinical research, and advanced cell therapies. Azenta's mission focuses on helping life sciences organizations operate with greater speed and precision while maintaining sample integrity throughout the research continuum.