Supplier Quality Engineer

Here are the Job details for your review.

Job Posting Title : Supplier Quality Engineer

Job Location : North Haven, CT 06473

Employment Type : Contract

Job Duration : 12 Months

Job Description:

Must Have:

Bachelor’s degree in mechanical/production engineering with Min 9–12 years of relevant experience. • Strong expertise in DFM&A principles and manufacturing methods for plastics, metals, and packaging components & Systems. • Proven experience in analyzing project feasibility for cost savings and efficiency improvements. • Proficiency in CAD - Creo/SW and PLM/PDM tools (preferably Windchill). • Solid understanding of project management methodologies, including planning, tracking, and cross-functional collaboration. • Strong verbal & presentation skills for effective collaboration with global teams. • Well versed with MS Powerpoint, Excel for reports preparation, data analysis/advance operations. • Proficient in conducting Production Part Approval Process (PPAP) to ensure compliance with technical specifications and quality standards. • Skilled in performing detailed Root Cause Analysis to identify issues, implement corrective actions, and drive continuous improvement.

• The Supplier Quality Engineer is responsible for managing finished goods Contract Manufactured (CM) for Robotics Surgical Technologies.
• Primary duties are focused on all QMS related matters pertaining to supplier selection, processing supplier change request, part/process qualification, manufacturing, QMS development, and technical quality/service/costs improvements.
• Work with new and existing CMs/Suppliers to develop, implement, and maintain technical quality assurance systems and activities, including MSAs, PPAP, SCR, Quality Plans, Control Plans, and FMEAs.

Top 3 technical skills that are required for the role:

1. Lead, support, review and approve supplier change request (SCR), Validation, TMV, PPAP, SCAPA, QMS etc.

2. Work with new and existing CMs/Suppliers to develop, implement, and maintain technical quality assurance systems and activities Quality Plans, Control Plans, and FMEAs

3. Familiar with the Medical industry requirements such as ISO 13485, 21 CFR 820 standards etc.

Education Required:

• Years’ Experience Required: Bachelor’s Degree in Engineering/Scientific/Electronic or technical field
• Years’ Experience Required: Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years relevant experience.