Quality Engineer Salary at Machinetek Llc BETA

Job Overview: A Quality Engineer is responsible for overseeing and implementing quality control processes, procedures, and inspections to maintain and improve product quality. This position will focus on implementing quality control measures, supporting product verifications and process validations, and collaborating with cross-functional teams to drive continuous improvement in the additive manufacturing operations. This position plays a crucial role in ensuring products or processes are consistent in quality, meet customer expectations, comply with industry standards and regulations. These efforts contribute to reducing defects, minimizing rework, and enhancing overall product reliability and customer satisfaction. Reports to: Quality Manager. Essential Functions: Company Culture and Mission:  Consistently apply core values (Integrity, Impact, Dedication) to your decision-making process and interactions with others.  Uphold and contribute to the company’s quality policy commitment.

Role: Quality Engineer location: San Diego, CA 100% onsite 5 days a week. Contract W2 only! Duration: 6+Months Job Summary: Sr Quality Engineer is responsible for maintaining the quality assurance support for the picking, relabeling, and repacking of finished goods prior to shipments to external or internal customers. This person will partner with cross function members to ensure product quality and timely product delivery. Functional Responsibilities: 1. Core Quality Assurance Responsibilities a. Review, sign off on batch record, scan, and store daily batch records and line clearance records for reagent R&R process b. Manage and retain records for the R&R verifier qualification program c. Scan, upload, and physically store QMS records (i.e., EMS reports, training records, validation reports, etc.) per document retention policy d. Address issues pertaining to material master data and material manufacturing batch discrepancies e. Manage ABI-OEM material program including quarantining in

Henslee Recruiting Services has been retained by a Medical Device Manufacture with locations in North San Diego, CA. We are searching for multiple Quality Engineer’s and Supplier Quality Engineers with at least 5 years of quality assurance experience. As a key member of the Quality Assurance team, you will play an integral part in helping drive the medical technology industry forward through transforming patient care and creating better patient outcomes. These roles must work onsite five days a week. Role Summary: The Quality Assurance Engineer will be responsible for implementing and overseeing activities at our company's manufacturing location. This role will be responsible for ensuring the quality and reliability of our products and processes. The ideal candidate will possess extensive knowledge of engineering and problem-solving principles and be accountable for a wide range of complex activities related to designing, implementing, and maintaining quality assurance protocols and me

Position Title: Supplier Technical Engineer Location: San Diego, CA Salary Range: $110-140k (flexible) Duration: Perm Start Date: ASAP - 2 weeks from offer As the STE at this facility, you would: Have technical accountability for the assigned purchased parts from NPI (initial concept) through the product life cycle, including all aspects of quality management. Be able to understand top supplier technical issues and provide ideas and solution to resolve the most complex and challenging problems. Be responsible for communication of technical requirements with Supplier, design/drawing review, Configuration Management input, perform Baan functions, tooling management, Q-Notes, etc. Monitor supplier quality performance data and trends and collaborate with the Sourcing Specialist and Buyer to develop and implement strategies for supplier performance improvements, leveraging root cause analysis and corrective and preventative action methodologies. Provide input into casting, brazing and machi

The Opportunity Atraverse Medical is an innovative, medical device start-up developing flexible left-heart access technologies to streamline procedures and improve patient outcomes. We are currently looking for a Principal Quality Engineer to join our team! What you will do Develop, implement and maintain procedures for compliance to regulatory requirements, internal procedures, inspection & sampling documents concentrated on Atraverse Hardware. Develops and implements systems to improve the detection and prevention of quality failures. Process improvements; analyze nonconforming product/process/material issues. Provides guidance and training to Quality personnel and employees of the company regarding the Quality System. Receive, analyze and respond to customer complaints. Analyze complaint patterns and categories to develop strategies for company wide improvements. Participates in Quality planning- facilities and products: requirements, documentation and completion (overview/monitorin

Role: Staff Quality Engineer Contract W2 Only Location: San Diego, CA The Sr. Staff Quality Engineer is a contract role that will be responsible for leading a project to improve the Quality and compliance of the Dispensing Implementation process. This role will work with the Dispensing Implementation teams to document and suggest compliance-related improvements or changes to that process. The intent of this role is to bring the Dispensing Implementation process to a state of compliance that would pass an external regulatory agency inspection. Duties include: • Evaluating the Dispensing Implementation process against regulatory requirements associated with CFR 820.200 and international regulatory requirements. • Leading a cross-functional effort to develop and execute the plan to improve the compliance state of the process. • Communicate weekly status to the Quality and SDS leadership teams. • Compliance to all service record documentation requirements. Job Family Summary: Quality Engin

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Position overview: The Senior Quality Engineer will be responsible for providing quality engineering support and leadership for Manufacturing Process development and implementation. This position will work closely Manufacturing in the manufacture of disposable medical catheters in compliance with applicable regulatory and statutory requirement. Essential Duties and Responsibilities: • Oversee EO sterilization validation processes and ensure routine sterilization activities meet regulatory standards. • Support environmental monitoring and clean room verifications according to schedule and assist with excursion investigations. • Review and approve manufacturing validation test plans, protocols, and test reports. • Lead the completion of risk management deliverables, including process Failure Mode and Effects Analysis (pFMEA) and Control Plans. • Support and lead test method valid

**Job Description** In Command, Control, Communications, Computers, Intelligence, Surveillance, and Reconnaissance (C4ISR) Systems, you ll help develop systems that sense, control, exploit and disseminate actionable information to warfighters supporting a variety of missions. We are looking for a Program Quality Engineering Intern to implement tools and processes to ensure product or services meets the standards of quality including reliability, usability and performance. You must be a self-starting problem solver who will utilize your analytical skills to find innovative solutions to quality-related issues. Strong communication skills are essential to understand requirements and expectations, make progress reports and present findings. **Intern Responsibilities:** + Supportsoftware development and hardware production programs + Apply lean strategies to existing processes + Provide overall support to Program Quality staff on items highly visible to Leadership + Understand Quality stand