Quality Engineer II Salary at Werfenlife Sa BETA

Company Overview: Tympanogen is a medical device company based in Richmond, VA with a mission to improve healthcare by simplifying surgical procedures. We develop gel-based medical devices for the ear, nose, and throat industry and transform eardrum repair surgery into an office-based procedure. Job Summary: We are hiring a Quality Engineer II to ensure the development, production, and delivery of the Company’s medical devices meet customer needs in accordance with the Company’s quality management system (QMS) and regulatory requirements. This hands-on position reports to the Quality Systems Manager and works closely with multifunctional team members, combining quality engineering expertise with document control and continuous improvement initiatives. All activities are performed within an FDA 21 CFR 820 and ISO 13485 compliant quality management system (QMS), alongside additional, relevant standards. An ambitious candidate with a track record of successful medical device compliance wh

Job Description Title: Quality Engineering Reports to: VP of Development Engineering Starting Salary: $74,436/yr.+ (competitive pay) Office/On-site: Monday to Friday, 8AM - 4:30PM Benefits: Full time associates are eligible for benefits the first of the month following 30 days of service. Medical Insurance HDHP, HSA Plan - Employer Contribution of $1,040/yr. High/Low PPO FSA Dental Insurance Vision Insurance Employer Paid Basic Life Insurance Supplemental Life Insurance Employer Paid Short Term Disability Long Term Disability 401(k) 4% Employer Match up to $500 Quarterly Bonus Paid Time Off (accrued hours, 120/year) 9 Paid Holidays Continuing Education and Seminar Programs EAP Program Fitness Room Summary: Quality Engineer will drive a Culture of Quality and Continuous Improvement within the company by promoting adherence to the Quality System requirements across all departments. Quality Engineer is responsible for ensuring customer, company, and regulatory requirements are met or exce

We believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come. At Terumo we believe in the power of personal growth and will encourage you to get in the driver’s seat – progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what’s next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, sustainable solutions for patients. Join us, and help shape wherever we go next! Advancing healthcare with heart Job Summary: The Manufacturing Execution System (MES) Quality Engineer II position will work closely with the IT, Operations, Validation, and Engineering, tea

Senior Quality Engineer II - Manufacturing, Medical Device Location: Atlanta, GA Working Situation: Onsite Join a world leader in medical device innovation, transforming surgical care and improving patients' lives globally. The commitment to cutting-edge research and compassionate healthcare solutions ensures that every day brings new challenges and opportunities for growth. Be part of a team where your expertise and passion will drive impactful advancements in medical technology. We are seeking a Senior Quality Engineer II to join our esteemed global medical device company, celebrated for its groundbreaking advancements in product development. As a pivotal member of our team, you will ensure our products meet the highest quality standards and regulatory requirements. You will have the opportunity to work cross functionally and collaboratively with keys stakeholders at the site. If you have a passion for excellence and a drive to make impactful contributions in the industry, we want to

Quality Engineer II - Aerospace Manufacturing If you would love to be part of a company that is poised for substantial growth with opportunities for advancement then working for CPP and its subsidiaries may be the right fit for you! We have multiple facilities in Albany, OR and are a world class supplier of titanium components and castings for the aerospace industry. If you are selected to join our team you will enjoy benefits such as quarterly bonus, medical, dental, vision, 401(k), company paid life insurance, and other great benefits! Primary Purpose: The Quality Engineer is responsible for driving quality forward by effective communication both internally and externally. Duties and Responsibilities: Responsible for maintaining configuration control documentation through contract review and blueprint/specification control. Works independently. Manages Multiple customer accounts including OEM's and sub tiers. Can perform as a backup QE for additional customers. Work with Engineering

JOIN OUR TEAM @ AMPHENOL RF, the world's largest manufacturer of coaxial interconnect products for radio frequency, microwave, and data transmission applications, and a proven leader in enabling next-gen technology! Our global team of experienced engineers develops innovative solutions utilizing the most advanced manufacturing technology available, and we specialize in creating custom solutions that meet customer-specific design requirements. With consistent year over year growth, innovative technology, and a team that breeds success, we are always seeking top-tier, high-performing talent to join us! We are headquartered in Danbury, Connecticut, and a division of Amphenol Corporation (NYSE ticker: APH), an industry leader for more than fifty years. At Amphenol RF, you can expect a competitive salary and comprehensive benefits (medical, dental, vision, matching 401K, FSA, employer-paid life insurance), a favorable work/life balance, a generous PTO allowance and paid holidays, an engagin

Main responsibilities/day to day activities required for this role: NCMRs and CAPA executions, Front Line support, A3 initiation as part of problem solving What products (if any) will this role support? Stents What is your target years of experience? Min 2-3 years Will the contingent worker be working remotely or onsite, or both? This role is 100% onsite As a Quality Engineer II at our Manufacturing site, you will be at the forefront of driving excellence in our products and processes. You’ll leverage your experience to ensure our life-changing therapies meet the highest standards of quality, compliance, and reliability. This role requires you to be onsite Monday through Friday, providing you the opportunity to collaborate closely with cross-functional teams in a fast-paced, hands-on environment. Responsibilities may include the following and other duties may be assigned. Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially fi

Position Summary: Supports the manufacturing production operations and obtains Quality through the achievement of “Zero Defects” practices. Position Responsibilities: Develops and implements standards and methods for inspection, testing, and evaluation, utilizing knowledge in engineering fields, such as chemical, computer, electrical, or mechanical. Devises sampling procedures, and designs and develops forms and instructions for recording, evaluating, and reporting quality and reliability data. Establishes a program to evaluate analytical testing, equipment, facilities, precision measurements, accuracy measurements, and performance testing. Develops and implements methods and procedures for disposition of discrepant material, and devises methods to assess cost and responsibility. Compiles and writes training material and may conduct training sessions on quality control activities. Supports all organizational initiatives including Safety, Quality, Productivity and Cost. Specific Knowled