Quality Specialist I Salary at Arup Laboratories Inc BETA

Job Description Perform general product preparation, clean-up and stock work in the Meat department and provide customer service. Demonstrate the company's core values of respect, honesty, integrity, diversity, inclusion and safety. Responsibilities Perform tasks such as cutting, grinding, slicing, preparing, processing, trimming, tenderizing, sealing, packaging, wrapping, bagging, pricing, prefabricating, dating, labeling, scaling, merchandising, selling, serving customers, and other functions in accordance with company policies. Keep department temperature logs accurately updated and maintained. Stock and display meat items safely and in accordance with company standards. Check product quality; make sure it is rotated properly and fresh. Keep sales areas, backrooms, coolers clean and well organized. Keep carts, tools, and supplies in their designated areas and well organized. Keep floors, clean, safe, and free from clutter. Provide good customer and associate relations. Communicate e

**Become a part of our caring community and help us put health first** The Care Delivery Call Quality Professional works within the Engagement Marketing group. The Care Delivery Call Quality Professional will be responsible for auditing, training and monitoring the Tele Sales Agents who are responsible for converting Medicare eligible callers to patients. The Tele Sales Agents work with callers to answer questions, describe services, and sell prospective patients on the clinical care model. The Care Delivery Call Quality Professional ensures that quality and productivity standards are maintained while working independently. **Role Responsibilities** + Maintain Quality Assurance scorecard + Align with Training on curriculum, process and procedure, updates and enhancements + Document quality issues and performance measures + Monitor and evaluate the quality of inbound and/or outbound Telesales calls + Provide coaching and feedback to Telesales Agents **Use your skills to make an impact**

Description Schedule :Monday - Friday (40 hrs/wk)8:00 AM - 5:00 PM Department: Quality Systems & Support - 252 Primary Purpose : The Quality and Regulatory Affairs Specialist I monitors and coordinates organization-wide compliance to current requirements of all quality related regulatory, certifying, licensing, and accrediting agencies. The Quality and Regulatory Affairs Specialist I assists with the coordination and maintenance of the regulatory submissions for new certificates, licenses, and updates to laboratory director roles with accrediting agencies. They may operate as a primary point of contact with regulatory agencies including but not limited to: CAP, CLIA, CMS, FDA, NY, ISO, DNV, and California. The Quality and Regulatory Affairs Specialist I frequently supports regulatory activities and supports ARUPs quality management System (QMS). This may include maintaining accuracy of the laboratory activity menu, coordinating or oversight of proficiency testing functions, coordinatin

Job Title: General Production Worker *$20 Per Hour (day shift)* *$21 Per Hour (night shift)* Job Description The General Production Worker is a position in our Extrusion department. As a Downstream Operator, you will utilize standard tools and measuring devices to ensure that the final product meets customer specifications and to catch any basic abnormalities. You will be mainly responsible for making sure the final product is being wrapped around the reel in an even and neat manner while maintaining a check on the quality of the product. Responsibilities Utilize standard tools and measuring devices to ensure the final product meets customer specifications. Catch any basic abnormalities in the product. Ensure the final product is wrapped around the reel evenly and neatly. Maintain a consistent check on the quality of the product. Essential Skills Manufacturing and Production Experience General production knowledge Machine operating experience Mechanical assembly skills Experience with

Education/Special Training Required * Bachelor of Science, Engineering or related subject with 2 or more years of experience in a quality or engineering discipline in a manufacturing environment, or * Master of Science, Engineering or related subject with 0 or more years of experience in a quality discipline Qualifications/Work Experience Required Who We Want A Quality Engineer with the ability to drive quality and deliver results. Someone who is an advocate for quality and lean methodologies; a self-directed professional who can identify issues and communicate effectively to all levels within the organization; a medical device industry professional who is passionate about providing superior quality products to patients and customers. * Previous experience in a regulated environment desirable (e.g. Medical Device, Aviation, Aerospace, Automative, Defense). * CQE or equivalent course work / experience desirable * Proficient in understanding of Med Device manufacturing processes desirabl

**Job Description Summary** The Manager, Quality Assurance reports directly to the Associate Director, Plant QA and is responsible for managing the quality activities and personnel for multiple departments in the plant. The manager will coordinate efforts for corrective and preventive action, non-conforming material investigations, and internal and external audits. They will assure manufacturing and support areas are compliant to regulations, standards, and internal procedures. The manager will support continuous improvement activities for the manufacturing and quality systems. They will provide regular updates to management of trends from these areas and oversee training and development activities for quality personnel in area. **Job Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and its no small feat. It takes the imagination and passion of all of usfrom design an

Software Engineer Location: Salt Lake City, UT Duration: 6 mos Pay Rate: $60 ph (W2) Job Description Function: Core Responsibilities: Reporting to the Engineering Manager, this position is responsible for the design, implementation, verification and validation of software used in manufacturing and other tasks as assigned. Essential job functions: Specific Responsibilities: Provide sustaining engineering for internal manufacturing software in compliance with Controls process. Activities include: - Software Planning - Software Requirements - Software design, implementation, unit test and code review. - Software Verification and Validation. - Software Version and Defect management. - Software Release. Provide technical support for manufacturing engineering, quality and operations. Required skills: Job Requirements: Technical Skills: Experience: A minimum of five (5) years in the development of multi-threaded applications software using design patterns such as MVP. Strong experience in WPF

Company Overview Sleep Number is a sleep wellness technology leader. For nearly four decades, we have placed sleep at the center of wellbeing, improving over 15 million lives with our Sleep Number smart beds. We are guided by our purpose - to improve the health and wellbeing of society through higher quality sleep. This is exemplified through our 4,000+ mission-driven team members who passionately innovate to drive value creation through our vertically integrated business model, owning the process from start to finish, including selling in our over 650 stores nationwide. Our team members are encouraged to bring their whole selves to work, sharing their unique perspectives, backgrounds and skills with Sleep Number every day. Whether you are entering, returning or experienced in the workforce, we have a place for you. We hope you join us in creating the future through higher quality sleep. Position Purpose To assure the quality standards and processes are followed during the mattress ass