Supervisor, Quality Salary at Ormco Corp BETA

Hello, One of my clients is currently looking for a Supplier Quality Specialist. If you're interested or if your skills align with the role, please share your updated resume with me at sushma@intellectt.com or contact me directly at (732) 838-4956. Job Title: Supplier Quality Specialist Location: Irvine, CA Job Description: We seek a Supplier Quality Specialist to manage and enhance supplier quality processes and ensure compliance with regulatory requirements. Core Skills: Strong knowledge of supplier quality management processes Experience conducting supplier audits and assessments Excellent communication and negotiation skills Proficiency in quality control tools and methodologies Strong analytical and problem-solving abilities Responsibilities: Evaluate and qualify suppliers based on quality standards. Conduct supplier audits and assessments to ensure compliance. Collaborate with suppliers to resolve quality issues and implement corrective actions. Maintain supplier quality document

Lead (Senior/Principal) Regulatory Affairs and Quality Specialist Job Description Wave Neuroscience is seeking an experienced Regulatory Principal Lead with significant Quality Assurance expertise who can lead Wave forward in these important arenas. The ideal candidate is an exceptionally organized, methodical professional who has the experience necessary to take our products to the next level in accuracy, integrity, security, and safety. The specialist will be charged with moving Wave forward on its first FDA clearance, with QA program support that not only safeguards product quality but also fosters a culture in which all employees are actively engaged. Key Responsibilities: Responsible for ensuring the preparation, drafting, and maintenance of quality documents (records, plans and reports) in support of regulatory (FDA & MDR) submissions to ensure timely approvals and market release of products. Provide support to currently-marketed products as necessary. Maintain risk analysis/mana

About SCAN SCAN Group is a not-for-profit organization dedicated to tackling the most pressing issues facing older adults in the United States. SCAN Group is the sole corporate member of SCAN Health Plan, one of the nation's leading not-for-profit Medicare Advantage plans, serving more than 277,000 members in California, Arizona, Nevada, Texas and New Mexico. SCAN has been a mission-driven organization dedicated to keeping seniors healthy and independent for more than 45 years and is known throughout the healthcare industry and nationally as a leading expert in senior healthcare. SCAN employees are a group of talented, passionate professionals who are committed to supporting older adults on their aging journey, while also innovating healthcare for seniors everywhere. Employees are provided in-depth training and access to state-of-the-art tools necessary to do their jobs, as well as development and growth opportunities. SCAN takes great pride in recognizing our team members as experts i

Production Quality Specialist Department: Production & Test Employment Type: Full Time Location: Hawthorne, California Reporting To: Joe Popwoycz Compensation: $110,000 - $145,000 / year Description Venturi Astrolab, Inc. (Astrolab) is pioneering new ways to explore and operate on distant planetary bodies. We are focused on designing, building, and operating a fleet of multi-purpose commercial planetary rovers to extend and enhance humanity's presence in the solar system. We seek motivated, creative, and exceptional people to join our world-class team. We seek a meticulous and experienced Production Quality Specialist to join our dynamic team. The role involves ensuring that our manufacturing facility meets the highest standards of Quality and Reliability. The Quality Specialist will maintain our commitment to excellence, from component inspection to final assembly verification. What you'll do: Quality Assurance: Conduct rigorous testing and inspection of rover components and systems t

Working at Caplugs, you’ll find a team-oriented environment working to deliver best-in-class products and service to more than 24,000 customers around the world. Our customers trust us with their product production needs day after day, and that trust starts with our most critical asset – our people. We work to identify and develop talent, continuously focusing on innovation, learning and improvement to deliver on our promise to be the product protection partner our customers need to solve their challenges. Are you ready to be a part of our team? SUMMARY: Plans, coordinates, and directs the Company's Quality System to insure compliance to customer’s requirements. Responsible for overseeing the activities of the Quality Department by performing the following duties. ESSENTIAL DUTIES AND RESPONSIBILITIES: Other duties may be assigned. · Serves as the Quality Management Representative for the quality system. · Acts as project manager when upgrading the quality system. · Acts as project man

The position of the Transplant Quality Specialist will work with the designated Organ Transplant Programs to provide oversight and will assist in maintaining compliance with the requirements of the external agencies specifically related to transplant regulations as set by the Organ Procurement Transplant Network (OPTN) / United Network for Organ Sharing (UNOS) and CMS Regulations, Joint Commission, Intermacs, and the ESRD Network. The Transplant Quality Specialist will be responsible for spearheading and providing oversight to the development, coordination, implementation, and evaluation of quality improvement initiatives; taking lead on investigating reported internal and external events, transplant adverse events, and working with leadership and operations on corrective and preventative action plans; participates and may take lead in RCAs; participating in on-site surveys with OPTN/UNOS and CMS; responsible for patient chart audits, providing data feedback, and reporting transplant d

Under the direction of the TFC supervisor, the transplant financial coordinator (TFC) is a designated member of the multidisciplinary transplant team. His/her primary function is to assure transplant patients' medical services are covered by insurance. This includes: insurance verification, authorization submission, effective patient counseling of insurance plans, providing insurance guidance when patients have a lapse of insurance or are under-insured and solid understanding of the complexity of transplant benefits as dictated by different insurance coverage. S/he is responsible for accelerating patient financial clearance by following standardized process steps. The TFC is also expected to problem-solve in real time and provide appropriate insurance direction to patients and staff, as needed. The TFC will participate in team meetings and discussions related to complex cases, advancing operational throughput and process improvement to benefit patient care. S/he should possess analytic

Pay $50-$55 per hr. Looking for Registered Nurse or License Vocational Nurse with cath lab, interventional radiology, or surgical experience. Summary: The main function of a prod quality clinician is to provide clinical expert knowledge and clinical guidance to Quality Specialists to understand the nature of complaints and possible health risks. Key Responsibilities: • Analyze complex event interpretation, event investigation, proper coding, required regulatory reporting, and complaint closure. May review complaint conclusions/closure statements and/or customer letters. • Obtain and evaluate information from clinical specialists, sales staff, physicians, nurses and other hospital staff/customers, as needed to support complaint investigation and drive towards resolution • Analyze complex clinical evaluation reports (CER) regulatory submissions, regulatory agency requests, and/or management report including ad hoc report • Provide clinical input to Product Risk Assessments (PRA). • Provi