Associate Failure Analysis Engineer

Associate Failure Analysis Engineer Acton, MA 01720 $50.00

• $52.98 an hour
• Contract $50.00
• $52.98 an hour

•

Contract Job Title:

Associate Failure Analysis Engineer Location:

Acton, MA 01720

Duration:

3 Months

JOB DESCRIPTION

The Associate Failure Analysis Engineer plays an integral role in client's Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices. The position requires strong organization skills, attention to detail, ability to work in cross functional teams, and drive to accomplish departmental and company goals.

Responsibilities:

Perform moderately complex tasks to ensure compliance with quality standards. Partner with quality assurance engineers and other team members to ensure effective inspection and testing procedures are implemented and maintained. Generate, review and maintain Quality records in support of the Quality System, e.g., training, internal audits, NCR, and CAPA. Perform product testing and failure analysis. Review Lot Acceptance records and DHRs, create trend charts. Perform investigation triage and deep dive investigations to develop hypothesis for failure. Collect log quality data and trend results. Accountability for quality investigation and root cause analysis. Assist in gathering information during FDA and

ISO 13485

inspections. Evaluate process flow by applying Lean Six Sigma methodology to streamline. Trouble shoot new failure modes. Evaluate process and engineering controls to improve safety and efficiency. Perform other duties as assigned.

Education and Experience:

Minimum Requirements:

Bachelor's Degree in an engineering or scientific discipline , or equivalent experience.

Preferred Skills and Competencies:

Computer proficiency in MS office (specifically Excel) Electrical and mechanical background strongly preferred Experience creating and analyzing charts in MS Excel a plus Knowledge of Six Sigma, Lean, SPC, ASQ and/or ISO process controls a plus Prior experience working in a regulated industry (medical device) and/or experience working in a bio-hazard/lab environment preferred Preferred 2 years in a Quality related function, working with QSR and/or

ISO 13485.

Effective verbal and excellent technical writing skills. Excels at generating and maintaining organized and accurate records. Physical Requirements (if applicable): Sitting 70%, Standing 30% Frequent lifting