| Location | Arden Hills, MA |
| Salary | $45–$50 |
Employment Type: Contract (13 Months) Onsite
Job ResponsibilitiesProvide hands-on quality engineering support to medical device manufacturing and production teams.
Investigate manufacturing process issues, identify root causes, and implement effective corrective actions.
Independently manage CAPAs from initial investigation through implementation and effectiveness verification.
Lead nonconformance investigations, including root cause analysis, impact assessments, containment, and corrective action planning.
Work closely with Manufacturing Engineering, Operations, and Quality teams to improve manufacturing processes and product quality.
Provide technical guidance to production personnel on quality requirements, process deviations, and troubleshooting.
Lead manufacturing process changes, including documentation, risk assessments, approvals, and implementation.
Evaluate process changes for their impact on product quality, manufacturing performance, and regulatory compliance.
Support change control activities and ensure compliance with established quality management systems.
Identify recurring quality issues and implement sustainable process improvements.
Maintain accurate investigation records and quality documentation in accordance with applicable medical device standards.
Bachelor's degree in Engineering or a related technical discipline, or equivalent relevant experience.
Strong experience in Quality Engineering within a regulated medical device manufacturing environment.
Proven ability to independently manage CAPAs, nonconformance investigations, and root cause analysis.
Extensive experience supporting manufacturing processes and resolving production-related quality issues.
Strong understanding of manufacturing process controls, process changes, and quality management systems.
Experience working directly with production personnel, Manufacturing Engineers, and cross-functional teams.
Hands-on experience with Windchill, particularly document control, engineering changes, or quality processes.
Demonstrated experience executing process improvements and corrective actions.
Strong analytical, investigative, and systematic problem-solving skills.
Ability to independently manage complex quality issues and provide technical guidance.
Background in Electrical Engineering, Electronics Manufacturing, or Electromechanical Devices.
Experience manufacturing sensors, sensor-based products, or similar electronic medical devices.
Experience using SAP in a manufacturing or quality environment.
Familiarity with ISO 13485, FDA quality system requirements, and regulated manufacturing practices.
Knowledge of 5 Whys, Fishbone Diagrams, FMEA, and 8D problem-solving methodologies.
Health Insurance:
Medical, dental, and vision insurance options are available through a third-party provider. Employees are responsible for paying the full cost of their insurance premiums.
Retirement Benefits:
A 401(k) retirement savings plan is available. No employer matching or other employer contributions are provided.
Paid Time Off (PTO):
No PTO other than that required by applicable state and local laws.