Associate Test Engineer

Cytiva

Marlborough, MA

Full Time

Entry Level

60k-80k

23 days ago

Job Description

About the Role

The Associate Test Engineer is responsible for the verification and validation of systems and products to ensure they meet the required standards and specifications. This role involves planning, executing, and documenting tests, analyzing results, and managing defects. It supports line extensions of existing products and new product introductions (NPI) for the R&D team in Marlborough, MA. Working at Cytiva means being at the forefront of providing new solutions to transform human health, with a culture of belonging and continuous improvement, aiming to make a tangible impact in life sciences, diagnostics, and biotechnology.

Key Responsibilities

Develop comprehensive test plans that outline the scope, approach, resources, and schedule for testing activities.
Perform tests according to the test plans, including functional, performance, and reliability testing.
Analyze test results to identify defects and ensure that the system meets its requirements.
Track and manage defects throughout the testing lifecycle, ensuring they are resolved in a timely manner.
Model and design parts and assemblies in CAD, create and modify drawings.
Work closely with other departments, such as development, quality assurance, and project management, to ensure seamless integration and delivery of products.

Requirements

Bachelor's degree in Biomedical, Chemical, or Mechanical Engineering, or related field.
0-2 years' post academic experience in engineering, bioprocess or related field.
Experience with working within an ISO 9001/13485 and/or cGMP environment, and with Risk Management ISO 14971.
Knowledge in statistical analysis, DOE, impact assessment, root cause analysis, and risk management/FMEA.
Experienced using CAD and PDM systems such as Solidworks, Inventor/Vault, and/or Creo/Windchill is a plus.
Understanding of Bioprocess Engineering principles and methodology.
Effective written and verbal communication skills, with the ability to work collaboratively across all levels within a global, multidisciplinary team.

Nice to Have

Previous experience in a regulated laboratory environment.
Experience working in a regulated laboratory environment.

Qualifications

Bachelor's degree in Biomedical, Chemical, or Mechanical Engineering, or related field.

Benefits & Perks

Comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k).
Eligible for bonus/incentive pay.
Flexible, remote working arrangements for eligible roles.

Working at Cytiva

At Cytiva, a Danaher operating company, the culture emphasizes belonging, continuous improvement, innovation, and making a tangible impact in human health. The company values diversity, inclusion, and flexible work arrangements, fostering an environment where employees can develop and contribute to meaningful challenges.

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