Overview
Quality Engineer Jobs in Acton, MA at SARACA
Title: Quality Engineer
Company: SARACA
Location: Acton, MA
Company Description
SARACA is a global engineering R&D services company, partnering with 25+ Fortune 500 customers across diverse industries like MedTech, Aerospace, Rail, Automotive, and more. As an ISO 13485 certified organization, SARACA specializes in the design and development of innovative medical devices, excelling in areas such as embedded software, UI/UX, mechanical systems, and product testing. With expertise in regulatory standards like IEC 62304 and EU MDR, SARACA serves as a trusted partner for compliance and technical documentation in MedTech. The company boasts a team of over 400 skilled engineers and consultants, delivering exceptional results for projects globally. Committed to innovation and learning, SARACA fosters a culture of growth and inclusivity as an equal-opportunity employer.
Role Description
This is a contract, on-site Quality Engineer role based in Santa Clara, CA. The Quality Engineer will be responsible for overseeing quality engineering, quality assurance, and quality control processes to ensure products meet established standards. Daily responsibilities include developing and implementing quality management strategies, conducting product quality assessments, addressing compliance issues, and collaborating with cross-functional teams to improve processes. The role requires a proactive approach to maintain the highest quality standards.
Qualifications
- Proficiency in Quality Engineering and quality improvement methodologies
- Experience in Quality Control and inspections to ensure compliance with standards
- Solid understanding of Quality Assurance and implementation of effective quality systems
- Expertise in Product Quality and continuous monitoring to maintain product excellence
- Strong skills in Quality Management processes and tools
- Ability to work collaboratively with cross-functional teams and adapt in a fast-paced environment
- Bachelor’s degree in Engineering, Quality Management, or a related field
- Previous experience in regulated industries such as MedTech, Automotive, or Aerospace is advantageous
- Knowledge of ISO 13485 and familiarity with regulatory standards like FDA, IEC 62304, or EU MDR is a plus
