Mechanical Engineer-Zwick Testing Systems

Job Title: Mechanical Engineer Zwick Testing Systems
Location: OH Onsite
Duration: Long-Term Contract
Employment Type: Contract W2
Pay Rate: $65/hr(DOE) on W2
Industry: Pharmaceutical / Drug-Device Combination Products
Experience: 7+ Years

Job Summary:
We are seeking an experienced Mechanical Engineer to support the operation, troubleshooting, testing, and validation of Zwick testing machines within a regulated pharmaceutical/life sciences environment. The ideal candidate will have hands-on experience with Zwick equipment, mechanical testing, failure analysis, validation, and test data analysis.

Job Responsibilities:

• Serve as the SME and system owner for Zwick testing machines.

• Support day-to-day operation, troubleshooting, testing, and validation activities.

• Troubleshoot testing equipment failures using established methodologies and procedures.

• Analyze test data to identify root causes and distinguish true failures from false failures.

• Support equipment and test method qualification/validation activities.

• Investigate equipment, product, and testing-related failures.

• Partner with Quality, Validation, Manufacturing, and Engineering teams to resolve testing issues.

• Ensure testing activities and results are properly documented in accordance with quality requirements.

• Support continuous improvement of testing processes and equipment reliability.

Job Requirements:

• 7+ years of experience with mechanical testing equipment or pharmaceutical/life sciences device testing.

• Hands-on experience with Zwick/ZwickRoell testing machines is highly preferred.

• Bachelor s degree in Mechanical Engineering or a related engineering discipline.

• Experience with drug-device combination products, medical devices, or pharmaceutical product testing.

• Strong knowledge of mechanical testing methodologies and equipment troubleshooting.

• Experience with test method/equipment validation and qualification.

• Strong experience with root cause analysis, failure investigation, and data analysis.

• Knowledge of GMP/GxP regulated environments.

• Strong technical documentation, analytical, and problem-solving skills.