Quality Analyst Salary at M&C Specialties Co BETA

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

Job Tittle: Quality Control Analyst II Location: Fort Washington, PA, 19034 Duration: 15 Months Pay Range: $(39.00 - 40.70)/hr on W2 Job Description: Responsible for using data to determine reliability and conformance of quality control process. Accountable for identifying trends and reoccurring issues and suggesting solutions. Duties & Responsibilities: Compiles and analyses data on reoccurring product defects to determine root cause. Documents analysis results. Analyses raw material inspection logs for consistent failures. Notifies purchasing and quality departments about suppliers that have provided inferior products. Studies work processes, measurements and performance metrics to identify improvement areas. Recommends new or modified procedures based on findings. Interfaces with customers, suppliers and associates to define and improve quality standards and expectations. Participates on process improvement teams. Monitors and scrutinizes internal and external complaints and compile

Immediate need for a talented Quality Control Analyst 2 . This is a 12+ Months Contract opportunity with long-term potential and is located in Fortwashington, PA (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID:25-63901 Pay Range: $35 - $40.70/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Compiles and analyzes data on reoccurring product defects to determine root cause. Documents analysis results. Analyzes raw material inspection logs for consistent failures. Notifies purchasing and quality departments about suppliers that have provided inferior products. Studies work processes, measurements and performance metrics to identify improvement areas. Recommends new or modified procedures based on findings. Interfaces with customers, suppliers and associates to define and improve quality standards and ex

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 Description Job Description Duties: Perform daily GMP Quality Control laboratory testing activities at the facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform environmental monitoring of the cleanroom areas as scheduled. Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Act as subject matter expert (SME) on one or more assays and train new laboratory personnel. Support generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs, and change control Qualifications: Bachelor’s degree in a relevant discipline (biological sciences or equivalent) 3-8 years of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus. Hands on experience in bioburden, endotoxins, mycoplasma, gram

Job Description Job Description Duties: Perform daily GMP quality control laboratory testing activities Perform data analysis and final result reporting to support product lot release with adherence to turnaround times Perform all activities with respect to GMP compliance Support thorough GMP investigations for out of specification test results Support product stability programs including execution of stability testing, stability data analysis, and final reporting of stability data Qualifications: Bachelor’s degree in a relevant discipline (biological sciences or equivalent) Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control role Hands-on laboratory experience with cell counting, cell viability, flow cytometry, ELISA/potency assays, endotoxin, and/or sterility techniques. Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance – PPO, HMO & HSA Dental & Vision insurance 401k plan

Job Description Job Description Duties: Perform daily GMP Quality Control laboratory testing activities at the facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. Perform environmental monitoring of the cleanroom areas as scheduled. Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Support technical problem-solving for issues pertaining to GMP Quality Control Support product stability programs, including execution of stability testing, stability data analysis and trending, and final reporting of stability data. Qualifications: Bachelor’s degree in a relevant discipline (biological sciences or equivalent) 0-3 years of experience in the pharmaceutical industry within a Quality Control role; experience with cell therapy products is a plus. Experience in bioburden, endotoxins, mycoplasma, gram stain, environmenta

LOCATION 4287 Route 130 S Edgewater Park NJ US 08010 Overview As the IT - Manager of Quality Assurance/Quality Control at Burlington, you will develop and implement a comprehensive Information Technology QA/QC strategy aligned with our goals. You'll establish quality goals, mentor a team of QA/QC professionals (both in-house and third party resources), and drive process improvement to ensure we maintain and enhance our quality standards. A Day In The Life... Quality Management Leadership Develop and implement a comprehensive QA/QC strategy aligned with the organization's goals and objectives. Establish and communicate quality goals, performance metrics, and benchmarks to the QA/QC team and cross-functional departments. Lead, mentor, and manage a team of QA/QC professionals, fostering a culture of continuous improvement and accountability. Process Improvement Identify areas for process enhancement and efficiency gains within the QA/QC lifecycle. Collaborate with cross-functional teams t