Supplier Quality Engineer at Tegra Medical Holdings LLC
Franklin, Massachusetts, United States -
Full Time


Start Date

Immediate

Expiry Date

24 May, 26

Salary

90000.0

Posted On

23 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Supplier Quality Engineering, Process Engineering, Supplier Monitoring, Nonconformance Management, Supplier Audits, Risk Analysis, Process Validation, PFMEA, Control Plans, Blueprint Reading, GD&T, Root Cause Analysis, Minitab, GMP, FDA, SOP Standards

Industry

Medical Equipment Manufacturing

Description
Job Summary The Supplier Quality Engineer is responsible for ensuring that the manufacturing facility's supplier's materials, processes, and final products are all high quality.  The SQE role utilizes Quality & Process Engineering principles, tools, and practices to monitor, qualify and manage suppliers to support the overall business and quality vision of Tegra Medical.    Role and Responsibilities * The individual must be capable of working independently and in a team, supporting the Quality, Production and Purchasing groups.  * Evaluating suppliers for compliance to minimum standards required to be added to Tegra's Approved Supplier List (ASL) * Monitor supplier performance and ensure timely responses to supplier nonconformances, SCARs or any other supplier quality issues.  * Evaluate and provide guidance to suppliers for approval of process changes requested by supplier or on behalf of Tegra's request.  * Complete supplier scorecards on regular intervals to provide feedback to the supplier as well as Tegra Purchasing and Production on supplier's performance.  * Complete supplier audits on intervals defined based on risk to ensure supplier's conformance to Tegra's ASL requirements.  * Work with Procurement to consolidate ASL between Tegra facilities to minimize the work required to maintain suppliers in multiple Tegra site locations.  * Eliminate redundancy in the ASL where applicable to reduce the overall number of active suppliers.  * Determine incoming inspection needs for purchased raw materials, component, etc. to meet Tegra's quality system or customer requirements.  * Engage suppliers in Environmental, Health and Safety (EHS) initiatives to determine compliance to ESG standards (where applicable). * Determine potential cost savings with suppliers based on minimum order quantities, process capabilities and incoming inspection requirements.  * Work with GTC, NPI and engineering to determine appropriate suppliers needed for product development.  * Additional duties and responsibilities as required. Qualifications   * Strong engineering skills, problem analysis/solving.  * Excellent written and oral communication skills.  * Understanding of GMP, FDA and SOP standards, guidelines, and regulatory requirements.  * Ability to work in a fast-paced manufacturing environment while managing multiple projects.  * Strong engineering skills with working knowledge of the following: Process validation and verification activities. (IQ, OQ, PQ, PPQ). Risk analysis techniques, which include PFMEA (Process Failure Modes and Effects Analysis).  * Manufacturing Control Plans and Flow Plans.  * Blueprint & GD&T reading. Problem solving techniques, including root cause analysis, and cause and effect analysis.  * Proficiency with Microsoft Office products (Word, Excel, Project, PowerPoint) and Minitab.  * Experience in the Medical device is highly desired.  * Hands-on experience in the manufacturing, quality & process disciplines.  Education Requirements A minimum B.S. in an engineering discipline preferably mechanical engineering or 5 + years' experience in a quality engineering equivalent role.    Physical Requirements * Frequent performing repetitive work. * Occasional lifting (max. 40 lbs.) * Occasional carrying (max. 40 lbs.) * Subject to physical hazards from moving equipment and machine parts. * Constant safety glasses. * Constant full PPE. * Frequent standing. * Occasional sitting, walking, pushing, pulling, reaching. * Regular attendance in the office is required Standard Office Hours
Responsibilities
The Supplier Quality Engineer ensures high quality of materials, processes, and final products from manufacturing facility suppliers by utilizing Quality & Process Engineering principles to monitor, qualify, and manage them. Key duties include evaluating suppliers for compliance, monitoring performance, managing nonconformances, completing audits, and collaborating with internal groups like Quality, Production, and Purchasing.
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