Hire Top Quality Engineer Intern

Robert Sharp

Results-driven Quality Systems Engineer at Stellant Systems Inc., adept at managing QMS per AS9100 standards. Expert in quality audits and corrective action, successfully streamlined procedures during company mergers. Proven ability to develop training programs and enhance compliance, fostering collaboration across departments to exceed customer expectations.

JAMES STYDINGER

Qualified and experienced professional with over 40 years of proficiency in the natural gas industry. Highly skilled at supervising construction and maintenance crews and handling customer service. Skilled and dedicated with expertise creating permits, driving utility vehicles, and ordering/controlling inventory. Results-oriented and self-motivated individual that collaborates easily with management and employees to meet deadline goals. Exceptional communication, leadership, and organizational qualities. Dependable and able to handle multiple tasks and prioritize job duties.

OSCAR MARIO VINDAS SALAS

To join an organization where analytical skills, customer service, and quality assurance experience could be fully utilized. Prefer an Information Systems environment, although I am open to new and challenging opportunities.

R. Gregory Bayly

Quality engineering professional with extensive experience at Woodbridge Foam, specializing in quality assurance and supplier development. Demonstrated success in process improvement and data analysis, resulting in significant enhancements in product quality. Skilled in leading cross-functional teams and building strong supplier relationships to ensure compliance and operational excellence.

Ron Alderson

Known as a results-oriented, self-starter, fast learner and innovative problem-solver. Demonstrates strong analytical, communication, and teamwork skills, with proven ability to quickly adapt to new environments. Eager to contribute to team success and further develop professional skills. Brings positive attitude and commitment to continuous learning and growth.

Julio Dominguez

I am an accomplished and detail-oriented Medical Device Quality Engineer with extensive expertise in FDA 21 CFR Part 820 and ISO 13485 standards. I am seeking remote, hybrid, and on-site opportunities to leverage my knowledge in the field of quality engineering, with a willingness to travel and relocate as needed. My career features a proven track record in implementing quality engineering systems and conducting inspections, testing, and audits to ensure regulatory compliance and maintain high-quality standards. I excel in identifying and mitigating risks associated with medical devices, prioritizing patient safety. My strong communication skills and collaborative approach foster cross-functional teamwork and drive continuous improvement. I am committed to staying updated on industry trends and regulatory changes to contribute effectively to any medical device organization.

Frances Castillo

Detail oriented quality assurance lead with 20+ years of experience working with team leaders to ensure products meet or exceed customer requirements for successful sell-off. Skilled at building trust among program managers and teams as a crucial team player to ensure inclusion in all phases of the program from kick-off to sell-off, resulting in excellent customer satisfaction reviews and meeting award fee targets. Excellent leadership skills focused on risk management and problem resolution through root cause analysis to resolve or mitigate issues, as well as focused audits to ensure compliance with program and customer requirements. Top-notch mentorship, communication, and coordination of test witnessing for multi-day, multi-test, multi-location test events resulting in successful SQT, SIT, and FQT outcomes. Experienced in Business Acquisition and Supplier Assessments supporting proposals, creating BOEs, technical volume review, requirements compliance matrices, creating supplier SOWs, flow down of requirements, supplier audits and action reviews.

Basma Hassan

Strategic Engineering Leader with excellent track record of successfully navigating teams through technical challenges to deliver quality medical devices into the marketplace. Experienced in collaborating and influencing to innovate solutions that result in positive outcomes for patients, medical professionals, and corporate stakeholders. Experienced in hands on medical device development through all stages of design control, project management including design input development, design output documentation, verification and validation, regulatory submission, and post-market surveillance.