Senior Quality Engineer: Aerospace & Medical Devices

enVision Staffing Solutions; New Bedford (MA); On-site; USD 100,000 - 140,000; Full time

Benefits offered by this job

Medical benefits start day 1

3 weeks PTO

5 days sick leave

401k match

Job summary

enVision Staffing Solutions is assisting a global engineering and manufacturing client with a Senior Quality Engineer role in Massachusetts, southeast of Providence. The position focuses on aerospace and medical components, including ceramic-to-metal seals, with a direct-hire path.

You will drive product and process quality across operations, lead investigations, and manage regulatory interfaces while maintaining the QMS.

Qualifications

• Bachelor's degree in Engineering (Mechanical, Electrical, Chemical) or related field.
• 5-10+ years of experience in manufacturing quality engineering.
• Aerospace and/or medical device experience strongly preferred.
• Strong working knowledge of CAPA, MRB, NCMR, RMA processes.
• Statistical tools (SPC, DOE, Minitab or equivalent).
• Experience with ISO 13485 and/or AS9100 quality systems.
• Familiar with handling Controlled Unclassified Information (CUI) under ITAR/EAR/NRC.

Responsibilities

• Drive product and process quality performance across manufacturing operations.
• Own complex investigations and lead customer and regulatory interactions.
• Ensure the effectiveness of the Quality Management System.
• Lead cross-functional quality initiatives in aerospace and medical sectors.

Skills

Quality engineering experience

Regulatory interface

Investigations leadership

Education

Bachelor's degree in Engineering

Tools

CAPA processes

MRB/NCMR/RMA

SPC/DOE/Minitab

ISO 13485/AS9100

Job description

enVision Staffing Solutions is assisting a global engineering and manufacturing client with a Senior Quality Engineer role in Massachusetts, southeast of Providence. The position focuses on aerospace and medical components, including ceramic-to-metal seals, with a direct-hire path.

You will drive product and process quality across operations, lead investigations, and manage regulatory interfaces while maintaining the QMS.