table>| Enable Skills-Based Hiring | No |
| Business case justification | |
| Increase in workload |
|---|
| Fast paced environment, working in an open concept area (able to focus with possible multiple distractions), problem solver and be resourceful to find solutions on your own |
|---|
| Office and Manufacturing environments. Must wear safety gear when on the manufacturing floor |
|---|
| Are there any safety risks associated with the role? | |
| No |
|---|
| Will the worker be working at a customer's facility? | |
| No |
|---|
| Essential Requirements of the Role | |
| " 3 7 years of experience in quality assurance within manufacturing or industrial environments.This Quality Assurance position works closely with Quality Assurance leadership to assess and improve manufacturing processes through testing, inspection, and verification activities. High School Degree or equivalent and 5+ years of quality assurance experience in in the manufacturing, assembly, and testing of critical hardware. JOB SUMMARY: The Educator and Quality Assurance Specialist for the Sterile Processing Department works to promote the development of a motivated and cohesive team and supports educational strategies to enhance staff knowledge with respect to processing practices and service delivery. Monitors all Sterile Processing Department quality systems and performs necessary audits for compliance practices, instrument sets in the Decontamination area, Assembly, Sterilization, Storage, and Case Cart preparation. li>Support turnaround events: print work packages, track inspection costs, update wall charts and QA spreadsheets, and perform general QA administrative functions. - Manage and enter inspection data (including PSV inspection and test data) in Meridium, ensuring accuracy, completeness, and audit readiness.
Houston, Texas30+ days ago We will consider for employment qualified applicants with criminal histories, consistent with applicable law.To learn more please visit: www.corebridgefinancial.com. The analysts also partner with various other teams including the training team, the client forms team, and various project teams to ensure appropriate communication and partnership to achieve optimal client satisfaction as well as employee retention and engagement. p>Our client is seeking a Quality Assurance Specialist to support quality systems, compliance, auditing, documentation, and continuous improvement initiatives within a manufacturing environment. Manage document control processes, including versioning, approvals, distribution, and employee access to current documentation. Works as the main point of contact for WRB manufacturer inspections, to include mock-up reviews and pre- construction meetings / final closeout of field inspection reports and warranty. The Quality Assurance Specialist is responsible for coordinating TCR development and quality directives by performing as an Owners Field Representative for the TCR Senior Managing Director/Managing Director of Multi-Family Development. In addition to exceptional written and oral communication skills, the RQAS will be working with a variety of audiences to include research leadership, administrators, principal investigators, and research staff, and will need to be proactive in engaging relationships and building lines of communication to effectively generate and disseminate pertinent research communications. Education: - Bachelor’s degree or greater in a Scientific Discipline, Business Administration, Health Care Administration or related field or four years of relevant work-related experience in health care or medical/academic setting can be substituted in lieu of a degree.
p>The fraudulent LinkedIn messages and emails, which do not originate from any Executives LinkedIn account or of UnitedHealth Group's email domains, or those of any of its operating divisions, supposedly conducts an interview via a Zoom meeting, offers a work from home job at Optum, emails an application, sends a fake check by next day delivery through USPS and asks recipients to pay a vendor a large dollar amount. Primary Responsibilities: - This position supervises Enrollment Analysts, Billing Coordinator, Coordination of Benefits Analyst and/or Team Leads for Medicare Advantage and Commercial Plans, managing daily assignments, productivity, and CMS file processing.
This role provides QA oversight on the production floor, supports batch disposition activities, and collaborates with cross-functional teams to maintain cGMP compliance. The position also supports investigations, deviations, and change controls while ensuring timely and accurate review of GMP documentation in a fast-paced manufacturing environment. This role provides QA oversight on the production floor, supports batch disposition activities, and collaborates with cross-functional teams to maintain cGMP compliance. The position also supports investigations, deviations, and change controls while ensuring timely and accurate review of GMP documentation in a fast-paced manufacturing environment. li>Coordinate and document Management of Change (MOC) activities affecting processes, materials, or products. Identify opportunities for process improvement using tools such as Lean, Six Sigma, or root cause analysis. Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies & in-depth understanding of site level products & related processes • Demonstrated expertise to effectively communicate within all levels of the organization around concepts of Repair/services controls, Repair/services verification and validation activities; production &process controls; Corrective & Preventive Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc. DMIAC, SPC, Lean SS, 5S, 8D) • Experience leading and implementing change • Experience performing internal and external audits • Exceptional analytical, problem solving & root-cause analysis skills • Ability to multi-task & handle tasks with competing priorities effectively • Strong technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures), global regulatory experience & demonstrated experience interfacing with regulators. The annual allocation to the ESOP is fully funded by BDO through investments in company stock and grants employees the chance to grow their wealth over time as their shares vest and grow in value with the firm's success, with no employee contributions. The Lead Engineer leads the development and execution of comprehensive test plans, while mentoring junior team members and collaborating with cross-functional teams to deliver high-quality solutions. For positions in Washington State, Maryland, or to be performed Remotely, click here or copy/paste the link below for paid time off benefits information: https://www.compass-usa.com/wp-content/uploads/2023/08/2023_WageTransparency_ChartwellsHED.pdf. In this key leadership role, you will be responsible for ensuring a safe, compliant, and well-regulated campus dining environment by managing safety, health, and risk-management programs while aligning with federal, state, and UH System policies. In this position, you will assign and audit the accuracy of the ICD-10-CM and CPT codes to ambulatory, emergency center, observation, and day surgery records for purposes of billing, research, and providing information to government and regulatory agencies. Ascertains the accuracy of the physicians'' E/M and procedure coding to their documentation, completes the auditing reporting tool, and provides feedback to the education team and/or provider. p>Texas Children's comprehensive health care network includes our primary hospital in the Texas Medical Center with expertise in over 40 pediatric subspecialties; the Jan and Dan Duncan Neurological Research Institute (NRI); the Feigin Tower for pediatric research; Texas Children's Pavilion for Women, a comprehensive obstetrics/gynecology facility focusing on high-risk births; Texas Children's Hospital West Campus, a community hospital in suburban West Houston; Texas Children's Hospital The Woodlands, the first hospital devoted to children's care for communities north of Houston; and Texas Children's Hospital North Austin, the new state-of-the-art facility providing world-class pediatric and maternal care to Austin and Central Texas families. We have also created Texas Children's Health Plan, the nation's first HMO focused on children; Texas Children's Pediatrics, the largest pediatric primary care network in the country; Texas Children's Urgent Care clinics that specialize in after-hours care tailored specifically for children; and a global health program that is channeling care to children and women all over the world. p>Texas Children's comprehensive health care network includes our primary hospital in the Texas Medical Center with expertise in over 40 pediatric subspecialties; the Jan and Dan Duncan Neurological Research Institute (NRI); the Feigin Tower for pediatric research; Texas Children's Pavilion for Women, a comprehensive obstetrics/gynecology facility focusing on high-risk births; Texas Children's Hospital West Campus, a community hospital in suburban West Houston; Texas Children's Hospital The Woodlands, the first hospital devoted to children's care for communities north of Houston; and Texas Children's Hospital North Austin, the new state-of-the-art facility providing world-class pediatric and maternal care to Austin and Central Texas families. We have also created Texas Children's Health Plan, the nation's first HMO focused on children; Texas Children's Pediatrics, the largest pediatric primary care network in the country; Texas Children's Urgent Care clinics that specialize in after-hours care tailored specifically for children; and a global health program that is channeling care to children and women all over the world. Houston, Texas30+ days ago Review and approve GMP master documents and executed GMP documents from QC, manufacturing, material management, and any other department that supports lot production.Review and approve GMP master documents and executed GMP documents from QC, manufacturing, material management, and any other department that supports lot production. If youre ready to help turn our customers breakthrough ideas into viable therapies, we look forward to welcoming you on board. This role supports quality, operations, manufacturing and engineering teams by performing inspections, audits, and documentation reviews to maintain quality compliance. At TDW we put people first - that means working everyday to ensure the pipelines that run through our communities are operating safely and reliably. li>Coordinate and document Management of Change (MOC) activities affecting processes, materials, or products. Identify opportunities for process improvement using tools such as Lean, Six Sigma, or root cause analysis. li>The current base salary range for this position is expected to be between $110,029 and $165,044 annualized; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators. The Manager, GMP Quality Assurance, Clinical will be responsible for responsible for supporting and maintaining high quality levels on Agios Drug Substance and Drug Product by Contract Manufacturing Organizations (CMOs). p>Tests, inspects, and approves products and samples at various stages of the production process and compiles and evaluates statistical data to determine and maintain quality and reliability of products by performing the following duties. Sets up and performs destructive and nondestructive tests on materials, parts, or products to measure performance, life, or material characteristics. Galveston, TX30+ days ago p>Job Summary: The Clinical Research Study Auditor is responsible for conducting independent audits of clinical research studies to ensure compliance with federal regulations, Good Clinical Practice (GCP), Institutional Review Board (IRB) policies, and institutional research guidelines and policies. Minimum Qualifications: Bachelor's degree in healthcare administration, nursing, clinical sciences, or related discipline, and five years of clinical experience, including three years in clinical research. Coordinate and document Management of Change (MOC) activities affecting processes, materials, or products. Identify opportunities for process improvement using tools such as Lean, Six Sigma, or root cause analysis. |
|---|