Quality Analyst Salary at Lystloc Inc BETA

**Fraud Quality Review Analyst** **WHAT IS THE OPPORTUNITY?** The Fraud Quality Review Analyst is responsible in assisting in reviewing, assessing, and reporting on the effectiveness and quality of work performed by Fraud Specialists. Will conduct internal quality reviews including but not limited to call samplings, case reviews and any other quality review functions in the department to ensure that all Fraud specialists are providing high quality service to our clients while following processes and procedures. **What you will do** + Conduct quality reviews including call samplings and any other quality assurance functions in the department to ensure that all Specialists are providing high quality service to our clients by analyzing and providing feedback. + Assist management in reviewing, assessing, and reporting on the effectiveness and quality of work performed by Specialists. + Uses quality monitoring data management system to compile and track performance at team and individual le

10 Days of PTO / 6 Sick Days / Paid Holidays Compensation: $35.76/hr to $45.87/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Healthcare benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, financial protection benefits, as well as HSA, FSA, and DCFSA account options. 401k retirement account access is offered starting on the 90th day with employer matching after one year of service. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Required Skills & Experience -Minimum 2 years of relevant GMP work experience in a lab setting -Minimum 1 year of experience working with mammalian cell culture -Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA -Bachelor degree in Biology or Chemistry -Work

Job Description: We are seeking a 3rd shift QC Analyst In-Process Laboratory position supports the Quality Control In-Process and conducts biochemical, microbiological, and general chemical testing of in-process or final product samples submitted to the QC laboratories. The position requires analytical testing to be completed in compliance with all applicable procedures, standards and GMP regulations. This position requires high attention to detail, organizational leadership, interpersonal skills, a quality mindset, critical thinking, and technical writing skills. This position will be the shift leader and primarily work independently. Key Responsibilities: Perform analytical testing in compliance with applicable GMP regulations while maintaining a safe work environment in compliance with all applicable environmental, health, and safety regulations. Conduct biochemical, microbiological, and/or general chemical testing of raw material/utility, in-process, or final product samples submit

Here at Savista, we enable our clients to navigate the biggest challenges in healthcare: quality clinical care with positive patient experiences and optimal financial results. We partner with healthcare organizations to problem solve and deliver revenue cycle improvement services that enable their success, support their patients, and nurture their communities, all while living our values of Commitment, Authenticity, Respect and Excellence (CARE). Come join a leading revenue cycle management company and our growing family of cancer registry professionals! Savista is one of the largest employers of ODS professionals in the nation and we have many opportunities available across a variety of cancer registry roles. You'll work in an environment where you'll be supported by a team of strong and tenured colleagues, including our quality analysts and educators. Our focus is to help you meet your full potential and have a successful career in cancer registry, while also providing our clients wi

Job Title: Lab Instrument Coordinator Location: Malvern, PA Duration:12 Months+ Job Description: Lab operations responsibilities include but are not limited to: • Coordination and management of instrument onboarding and validation. • Facilitating instrument preventive maintenance, calibration, and repairs; may include some hands-on maintenance and calibration duties. • GMP record keeping. • Chamber management. • Lab safety and housekeeping. • Software validation • Be able to coordinate activities with internal and external operations and service teams, service providers, IT, site quality, and analysts to ensure lab operation activities are completed and compliant. Requirements: • Bachelor’s degree or equivalent, in Chemistry, Biochemistry or related subject area, with a minimum of 1 or more years related industry experience managing laboratory equipment. • Strong verbal communication skills are required. Demonstrates excellent interpersonal skills (written and oral) and the ability to

Job Description Job Description We are seeking a Supervisor- Workflow to join the team in our King of Prussia, PA office! The Supervisor - Workflow is responsible for overseeing the daily operations of the Workflow team, ensuring efficiency, accuracy, and compliance with company policies and industry regulations. This role involves supervising staff, optimizing workflows, and driving team performance to meet key metrics. The ideal candidate is a proactive leader with strong problem-solving skills, a collaborative mindset, and a commitment to continuous improvement. Responsibilities: Provide direction, support, and coaching to ensure the team meets departmental goals and performance standards. Oversee workload distribution, prepare daily assignments, and ensure turnaround time and service level agreements (SLAs) are met. Oversee claims setup, policy enrollments, and member eligibility verifications in accordance with company policies and regulatory guidelines. Track quality and producti

Compensation: $27-$33/hr Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Shift: 3/12h shifts - 6PM-6AM; rotates week over week! OT Available 10 PTO days, 6 sick days per 12 months, renewed upon extension. *Please note - sick days and PTO days cannot be used interchangeably, and do not carry over upon extension. Requirements: A minimum of a bachelors degree in chemistry, or a Scientific related field Minimum 1 year of working in current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify gaps in processes or systems Experience with HPLC, pH testing, Osmo testi

Compensation: $28-$34/hr Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. OT Available 10 PTO days, 6 sick days per 12 months, renewed upon extension. *Please note - sick days and PTO days cannot be used interchangeably, and do not carry over upon extension. REQUIRED SKILLS AND EXPERIENCE A minimum of a bachelor's degree in science or equivalent technical field is required. A minimum of two years of experience within GMP pharmaceutical industry and quality setting -Experience with SAP Skilled in basic understanding of LIMS systems. Knowledge and awareness of compendial requirements and standards