Quality Auditor Salary at Daikin Applied BETA

Q3 Contracting, a division of Primoris Services Corporation, is a publicly owned and operated const ruction contracting company that provides both specific and turnkey services for its customers in the gas, oil, electric and telecommunications industry. We are headquartered in Minnesota, with branch offices in Colorado, Wisconsin, Iowa, Nebraska, North Dakota, South Dakota, Ohio, Maryland, and Illinois Job Duties: Responsible for performing field audit functions. Complete daily documentation of field audits & evaluations. Assists with necessary employee training qualification functions. Accident and/or incident investigation & reporting. Provides direct engagement with crew activities in the field. Provides training and instruction to field employees on job sites. Provides input to management. Evaluates employee / crew performance relating to PDS and Customer standards, best practices and safety polices. Assist in developing performance objectives and standards. Maintain confidentialit

Quality Engineer • Location: Saint Paul, MN • Type: W2 contract (NO C2C OR THIRD PARTY) • Length: Until 12/2025 (Contract extension expectation) • Pay Rate - $33 hourly • Work Authorization - Must be able to work in the U.S. with approved authorization status. What You'll Do: Provide Quality Engineering support to manufacturing and new product development teams through Engineering Investigations, Qualifications and Validations. In this role you will identify quality issues, participate in quality improvement projects and quality activities that impact manufacturing. Additional responsibilities will include maintenance of on-going stability validations, nonconformance investigations, maintenance of risk management documentation, and corrective and preventive actions when required. Responsible for NCR and CAPA activities. Investigate and disposition nonconforming material reports NCR events. Initiate, investigate, and implement corrective and preventive actions as assigned. Perform inter

Job Description Job Description Hours: Monday-Thursday 6:15am-3:30pm, Friday 6:15am-12:15pm. Some Saturdays when needed 6:00am-10:00am Job Summary: Maintains systematic activities of the Quality System through inspection of products at various stages of production, evaluating statistical data, performing process audits, and monitoring quality, safety, productivity, and efficiency requirements. Essential Duties and Responsibilities: Inspector Duties Following processes and ensure adherence to best production practices and customer quality standards. Inspection of raw, in-process (WIP) and finished goods inventory parts to determine if they meet customer specifications. Track all defects related to part quality, material, subcontract operations and packaging for analysis. Conduct measurements and fill-out paperwork in support of FAIR submissions. Communicate with management and operators regarding quality problems or elevated risk of defects based on (inspection and) SPC data. Enter data

Position Overview: The Senior Quality Engineer ensures compliance with regulatory requirements (FDA QSR, ISO 13485, ISO 14971) and company procedures, contributing to both development and production teams to meet customer, company, and regulatory standards. The role includes process development, quality support, risk assessments, root cause analysis, and continuous improvement efforts. Key Responsibilities: Ensure adherence to Quality Management System (QMS) and regulatory standards. Provide support to either the Development or Production teams, ensuring product manufacturability, process qualification, and regulatory compliance. Develop, validate, and execute test methods, standard work, and process controls for new and existing products. Conduct risk assessments, quality plans, control plans, and root cause analyses to resolve issues and improve processes. Support process improvement, nonconformance investigations, customer complaints, and supplier quality issues. Lead or participate

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree. A company

Job Description Job Description Job Title: Quality Control Technician (2nd Shift) Position Type: Full-Time Evaluation-to-Hire About the Company: Our client is a leading manufacturer specializing in custom formulations for a variety of high-quality personal care and household products, including hair and skin care, and bath & body essentials like hand washes, lotions, shampoos, conditioners, and pet care products. With a commitment to quality, they offer both high-performance and certified organic formulations. Position Summary: We are currently seeking a motivated and self-directed Quality Control Technician to join our client's manufacturing team for the 2nd Shift, which operates Monday through Friday from 2:30 PM to 11:00 PM. This is a Full-Time Evaluation-to-Hire opportunity. The ideal candidate will possess experience in line audits, quality control (QC) testing, and microbiological testing, as well as hold a Bachelor's degree in Biological Sciences, Microbiology, or Chemistry. Key

Job Title - Sr Supplier Quality Engineer Job Location - Brooklyn Center, Minnesota Top 3 things you are looking for in a candidate’s experience: Quality control/engineering manufacturing / product / mechanical engineering Driving projects to closure / DMAIC / CAPA experience Job Description - Responsibilities may include the following and other duties may be assigned. Ensure that suppliers deliver quality parts, materials, and services. Qualify suppliers according to company standards and may administer a Certified Supplier Program by receiving inspection to ensure cost effectiveness. Monitors parts from acquisition through the manufacturing cycle and communicate and resolves supplier-related problems as they occur. Develops and prioritizes an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Evaluates suppliers' internal functions to assess their overall performance and provi

Job Description Job Description Position Summary: The Quality Assurance Document Control Specialist is a quality focused individual who ensures documentation and record keeping processes conform to cGMP and regulatory requirements, approved procedures, and ensures completed records are accurate and compliant. Assist in the day-to-day record management activities within Bell International Laboratories complying with company and regulatory requirements. Key Responsibilities: Perform QA document control functions, including document logging, tracking, processing, review, distribution, release and archiving of documents. Review, approve and formally release batch records that comply with requirements. Coordinate the revision, review, and approval and obsoleting of SOPs and other GMP documents. Responsible for ensuring compliance with document control requirements, such as periodic review of documents. Facilitate improvements to procedures by working with document owners to resolve conflict