Quality Assistant Salary at Viper BETA

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Role Description The Quality Inspector performs incoming inspection, in-process inspections, and final inspections of components and assemblies per control/quality plans. The Quality Inspector will review and approve final release documentation. Performs incoming inspections per control/quality plans for received materials. This role will also complete appropriate quality records within company and GMP guidelines, policies and procedures. Roles and Responsibilities: Inspect incoming or production materials for conformance to engineering drawings, schematics, and specifications; process standards and specifications; and production or process plans. Perform incoming test of components. Monitor for conformance to design or test specifications or standards. Accept or reject materials or articles; identify and document non-conformance and notify appropriate personnel of potential re

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. SUMMARY OF THE JOB The Senior Manufacturing Technician will support Engineering development and validation activities in addition to production support. This position will be a key contributor on Bolt’s Engineering team, developing a therapeutic medical device. Responsibilities: Demonstrate strong problem-solving skills and have the ability to ask critical questions without being the subject matter expert • Interact with Engineering to ensure that processes and designs are manufacturable • Design manufacturing processes, procedures and production layouts for assemblies, equipment installation and material handling • Fixture design and development including mechanical design, tolerance analysis and material selection • Strong problem-solving skills • Organization of equipment and spare part inventory • Maintain equipment documentation including manuals • Author IQ protocols and

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

DUTIES AND RESPONSIBILITIES Reviews and evaluates repaired and manufactured C4ISR electronic components, assemblies, and systems to ensure adherence to Depot Quality Management System (QMS) and ISO 9001:2008 / 2015. Conducts a variety of Quality Assurance (QA) tests and inspections, including final sell-off tests, in-process testing, solder testing, and pre-work inspections. Participates in establishing quality standards for life cycle maintenance, documentation, development methods, and testing. Develops and implements systems testing standards and procedures and conducts tests. Records and reports QA inspections and tests using established QA database. Documents and analyzes test results, and makes recommendations to improve overall quality. Assists with project planning activities associated with engineering projects. May provide quality-related training. Maintains current knowledge of relevant technologies as assigned. Participates in special projects as required. REQUIRED SKILLS/Y

Job Description Job Description PrideStaff has a great temp to hire opportunity with a medical device manufacturer in Carlsbad, CA Full Time - Monday - Friday 730am -400pm The position is crucial in that this person will be responsible for multiple activities, primarily hands-on production. Other responsibilities include shipping and receiving, and order entry into QuickBooks. The ideal candidate must focused energetic and willing to work with minimal supervision. Attention to detail is a must. Much of this work will be routine hands-on production. The primary objective is to maintain finished good inventory at designated levels. Other activities include interfacing with VP of Sales and customer service phone calls. Essential Duties and Responsibilities include the following. Other duties may be assigned.  Carry out standard operating procedures involving materials measurement, materials handling and inventory control, equipment operation and record keeping necessary to manufacture pr

About Us: Frontgrade is the largest provider of analog and radiation hardened technology for the United States aerospace and defense industry. From human spaceflight and space exploration, to missile defense and electronic warfare, to healthcare solutions addressing COVID-19, our talented team develop high performing electronic solutions that work the first time, every time. Are you looking to be part of the Space Evolution? Where innovation and ideas go hand-in-hand? Then come join the Frontgrade Team! Responsibilities: YOUR ROLE AND RESPONSIBILITIES Provide assembly with engineering leadership and guidance for the introduction and sustainment of processes, equipment and error proofing technology into assembly. Evaluate manufacturing processes by applying knowledge of product design, fabrication, assembly, test, tooling, and materials; conferring with equipment vendors; soliciting observations from operators. Assist in the estimation of manufacturing costs, determine standards, make r

DIRECT CANDIDATES ONLY, IF INTERESTED APPLY THROUGH JOB POST. NO DIRECT MESSAGES. RECRUITERS: DO NOT CONTACT. Position Overview: The Senior Manufacturing Engineer will support Engineering development and validation activities. This position will be a key contributor on Bolt’s Engineering team, developing a therapeutic medical device. Responsibilities: • Working understanding of statistics for process development including sample size selection, data distribution analysis, process capability, Design of Experiments (DOE), and Analysis of Variance (ANOVA). • Working understanding of inspection methods and procedures (Test Method Validation). • Demonstrate strong problem-solving skills and have the ability to ask critical questions without being the subject matter expert. • Interact with Product Development/R&D to ensure that processes and designs are manufacturable. • Design manufacturing processes, procedures and production layouts for assemblies, equipment installation and material hand

HME has been creating innovative products for the drive-thru and pro-audio industries since 1971. From the very beginning, we've known these solutions would never have happened without the customer-focused people who make up our company. HME has a team environment with a culture of collaboration, learning, and growth. With subsidiaries located in California, Georgia, Missouri, Canada, UK and China, companies around the world depend on HME for clear, reliable communication solutions. From setting the standard for drive-thru headsets and timer systems in the quick service restaurant (QSR) industry to developing professional audio equipment used in the Olympic Games, HME strives to create the newest, most innovative products on the market while providing quality care and attention to its customers. At HME you will have the opportunity to learn and grow while developing our future products. Come join our team! Are you good with your hands? Do assembly instructions make sense to you? Are yo