CAD Drafter Salary at Toweriq BETA

Job description: Quality Engineer II Location – Marlborough, MA (ONSITE) Duration: 6+ months Contract (Conversion possible for the right candidate) INTAKE NOTES: • Shift Hours: 8:30-5pm • Required Education: Requires a bachelor's degree in Engineering, Quality Assurance, or a related field • Required # of years’ experience: 3-5 Manager Notes: Supports Test Method Validation Remediation: Assists in the review and improvement of existing test method validation documentation Implements remediation plans to ensure test methods comply with current regulatory standards. Documentation and Compliance: Ensures validation documents meet FDA, ISO 13485, and other relevant regulatory requirements. Maintains accurate and organized records of validation activities. Qualifications: Requires a bachelor's degree in Engineering, Quality Assurance, or a related field. 3-5 years of experience in test method validation or a related area. Knowledge and Skills: Familiar with commonly used concepts, practices

Job Description: We are seeking an experienced Quality Engineer with a strong background in failure analysis within the semiconductor manufacturing industry. The ideal candidate will be responsible for ensuring the quality and reliability of semiconductor products throughout the manufacturing process. Key responsibilities include: Conducting detailed failure analysis and root cause investigations for defective semiconductor products. Collaborating with cross-functional teams, including design, manufacturing, and test engineering, to identify and resolve quality issues. Utilizing industry-standard tools and methodologies to perform failure analysis, data collection, and statistical analysis. Developing and implementing corrective and preventive actions (CAPAs) to address quality issues and improve product reliability. Supporting continuous improvement initiatives and driving quality standards across manufacturing processes. Assisting with the development and execution of quality control

Title: Quality Engineer II Location: Marlborough, MA Duration: 06+ Months Schedule: Regular Business Hours Job Description: Performs inspections and sets quality assurance testing models for analysis of raw materials, materials in process, and finished products. Requires a bachelor's degree and 0-2 years of experience in the field or in a related area. Has knowledge of commonly-used concepts, practices, and procedures within a particular field. Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision. Primary job functions do not typically require exercising independent judgment. Typically reports to a supervisor or manager. Supports Test Method Validation Remediation: Assists in the review and improvement of existing test method validation documentation Implements remediation plans to ensure test methods comply with current regulatory standards. Documentation and Compliance: Ensures validation documents meet FDA, ISO

Control Point Associates is seeking an experienced Survey Technician in our Southborough office. Competitive pay, excellent benefits, an amazing team and endless opportunities for overtime are just a few reasons why you should apply today!! Business is booming and were looking for the best and brightest Survey Technician in the industry to join our team in Southborough!! Take the first step towards the rest of your life in a supportive environment that promotes hard work and dedication! Essential Functions: + Oversee and mentor CAD Drafters review plans prepared by CAD Drafters for accuracy, completeness and conformance to company and client standards. + Assist and work directly with Assistant Project Managers and Project Managers. + Ability to create mapping from field crew data collector files (points), field sketches, digital photographs and reference maps. + Deed and reference map plotting. + Preparation and set-up of survey data for field crews. + Post survey field data analysis a

We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. KROHNE, Inc. complies with applicable federal, state & local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. KROHNE SUMMARY The Quality Engineer will leverage your technical expertise and knowledge of quality assurance to help drive continuous improvement in a collaborative environment which foster team growth. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Collaborate with department managers as needed to provide technical support for quality-related issues, conduct detailed root cause analysis, and implement effective solutions. Represent Quality when working c

Quality Engineer II 3 month contract Raynham, MA - onsite 5x a week Required Skills & Experience Industry: Minimum of 4 years of experience in medical device manufacturing or other highly regulated industries. Understanding of investment casting (foundry processing) is preferred but not required. Validation: Strong background in process validations (IQs, OQ/PQs, TMVs) is required. Quality & Compliance: Champions compliance to applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements). Raises Quality issues as appropriate. Proficiency in conducting non-conformance investigations and maintaining non-conformance records; strong investigation skills and ability to manage multiple investigations are essential. Experience in supporting Corrective and Preventive Actions (CAPA) preferred but not required; includes Action Plan (AP) and Effectivity Monitoring (EM) tasks. Change Control: Experience with change control processing via PLM system

JOB SUMMARY: Maintain the quality system and support outgoing product quality through the use of engineering tools and methodologies in order to support production, design, and development of medical devices. ESSENTIAL FUNCTIONS: The incumbent may be required to perform all or a combination of the following essential functions as determined by business necessity. Assist in the design and development of new products by contributing to risk analysis, verification and validation test plans, etc. Good understanding of statistical techniques, risk analysis, Gage R&R, Cpk, ANOVA and DOE. Good problem solving experience with Cause & Effect diagrams, Failure Mode Effect Analysis, Root-Cause, 5-Why, 8D. Approve Engineering Change Orders, review prints and be familiar with Geometric Tolerancing. Maintain Quality Records. Perform Corrective Actions and Non-conformance assessments. Assist in investigating customer complaints. Perform internal audits as well as supplier audits. Support Incoming Ins

Who we are With its A.I.-powered robotic technology platform, Symbotic is changing the way consumer goods move through the supply chain. Intelligent software orchestrates advanced robots in a high-density, end-to-end system - reinventing warehouse automation for increased efficiency, speed and flexibility. What we need As a Quality Engineer you will interface with manufacturing, supplier quality, engineering and test to drive high levels of quality and field reliability of our system. The candidate must be able to understand the application of our products and their use environments to appropriately and strategically apply technical knowledge, tools an methodologies to drive product quality. Applying statistical and reliability methods this position will examine the field data, bot health, subsystem/components defects, and site quality concerns. What we do The Quality team is part of the Manufacturing organization which is responsible for driving continuous improvement practices of our