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My client is seeking a dedicated Quality Systems Engineer to ensure quality standards and processes are effectively implemented and maintained in the industrial and manufacturing industry. This role involves developing, managing, and improving quality systems to support operational excellence in New Bedford.
This role focuses on developing and improving measurement systems, CMM programs, and quality processes to ensure consistent product performance and compliance with aerospace and customer standards. It supports both new product development and legacy process improvements through data analysis, process control, and collaboration across engineering and manufacturing teams.
Are you a Quality Engineering Professional who has strong ISO experience in the Medical Device Manufacturing industry? Do you have a Lead Auditor Certification in ISO 9001, AS9100, ISO 13485, ISO 14001, IATF 16949 etc.? Do you have a degree in Engineering or a related field? If so, please read on and apply to the Quality Systems Engineer (QMS)- Medical Device Manufacturing based near Fall River, MA.
Are you a CMM Programmer and/or Quality Engineer with a strong focus on CMM Programming? Do you have 2+ years of experience in the Manufacturing industry (ideally Aerospace and/or Plastics)? Do you have experience with Quality Inspections, GD&T, and vision systems? If so, please read on and apply the CMM Programmer/Quality Engineer - Plastics Manufacturing opening based near Fall River, MA.
The quality engineer will help lead all quality-driven activity associated with the design and manufacturing of precision medical devices and components. The ideal candidate will help lead all audits, handle QA/QC activity, and work cross-functionally with engineering teams to ensure product and customer standards are met.
The role oversees quality systems by leading customer complaint investigations, managing audits, and maintaining compliance with multiple industry standards. It also manages document control, calibration processes, and cross‑functional quality improvements while supporting external quality system interactions.
We are seeking a motivated Development Engineer to join a medical device organization. The ideal candidate will be responsible for developing and implementing engineering solutions to meet our project requirements, with a particular focus on applications related to medical device implants. This role involves designing and optimizing components that meet stringent regulatory standards and supporting innovation in implantable technologies.
This Product Development Engineer leads the design and development of instruments from concept through commercialization, ensuring meeting with industry standards. It involves close collaboration with the medical industry, cross-functional teams, and design engineers to deliver effective solutions.
This is a high level quality engineering position with a medical device manufacturer near the IL/WI Border. This role will engage in all QA/QC activity in metal fabrication environment.
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