Manager, Quality Salary at Pepco Manufacturing Co BETA

**_What Quality Assurance contributes to Cardinal Health_** Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Assurance develops and implements a compliant and cost effective quality system that assures products and services are reliable, safe and effective. This job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on Quality policies and procedures and ensures that all products and services are properly reviewed for quality and documented. **_Job Summary_** Position will oversee and enhance through continuous improvement the quality systems that support the repackaging of drug products, achieved through collaboration with contract repackagers. The position includes ensuring that the repackaged products meet the highest standards of quality and compliance. Closely moni

Job Description Job Description Quality and Regulatory Affairs Specialist Full Time, Permanent Opportunity Philadelphia, PA We are seeking an experienced, detail-oriented Quality and Regulatory Affairs Specialist to help ensure compliance with regulatory requirements and maintaining quality standards for our products. This role involves close collaboration with regulatory bodies, internal teams, and other stakeholders to ensure compliance with local, national, and international regulatory requirements. The ideal candidate should have a strong understanding of regulatory procedures and standards, such as ISO 9001, FDA regulations, etc. In this role, you will manage product submissions, maintain regulatory documentation, and coordinate internal and external audits. Overall Responsibilities include: Ensure company products comply with all applicable regulations and standards. Develop and manage quality assurance processes and documentation. Coordinate with regulatory bodies for product ap

A large healthcare insurance company is looking to hire a Quality Management Credentialing Analyst to their Final Optical Check Quality Management team. This person will work alongside the credentialing team and Board Committee to develop and update policies, audit and review processes, and assist in building out a strong provider base in both the physical and behavioral health field. Responsibilities include developing, implementing, and facilitating the regulatory and accreditation credentialing investigation process. They will Identify and analyze the credentialing processes for high-risk, high-volume and problem prone credentialing processes to mitigate risk and improve provider satisfaction. This person will use their previous credentialing background to recommend a plan of corrective action for resolution and follows up for adverse trends identified via data analysis. They will follow NCQA accreditation, CMS state and federal laws/regulations as well as internal policies We are a

Job Description Job Description Onsite- Sitka, Alaska Registered Nurse - Quality Management and Accreditation Job Description Summary- Provides and applies clinical knowledge and expertise; advanced critical thinking, knowledge of quality and accreditation. management tools, techniques and processes of a variety of federally or state mandated and/or consortium-wide driven processes. This position coordinates regulatory surveys; continuous accreditation readiness activities; facilitates significant clinical events investigations and reporting; participates in medical staff peer review and medical staff performance data support for hospitals and/or ambulatory setting; conducts medical record review, data analysis, trending and solutions, facilitates education and training around quality, accreditation and safety; chairs committees and teams as applicable, and serves as the expert for quality improvement and accreditation. This position works closely with Administration, Providers, Leader

Sr. Manager- Quality Location: East Coast (Relocation Required and Paid For) Are you a quality-focused leader passionate about improving product performance and ensuring exceptional customer satisfaction? We're seeking a Sr. Manager of Quality Engineering to lead initiatives that enhance product quality, resolve customer issues, and elevate operational standards. This role is based on the East Coast and will require relocation. Key Responsibilities As a Sr. Manager, you will oversee post-market quality operations, including: Leading product quality evaluations and root cause investigations based on customer feedback and field reports. Developing and monitoring performance metrics to ensure alignment with quality standards and identifying areas for improvement. Building and managing a customer-facing quality team to collaborate with sales and service teams, participate in field visits, and address quality escalations. Driving swift resolution of product quality issues, including recalls

Shift: Tuesday to Saturday from 11PM to 7:30AM Overview We are seeking highly motivated Manager, Quality Release, to join the facility’s Quality Operations team. The Quality Operations team will be responsible for ensuring that all operations at the facility comply with cGMP regulations, as well as internal policies and procedures. The Manager, Quality Release will work alongside manufacturing, QC, and Supply Chain, helping to ensure that the highest standard of work is performed. Shift: Tuesday to Saturday from 11PM to 7:30AM Essential Functions and Responsibilities Ensure compliance to cGMPs and facility procedures. Interface with functional groups, such as Manufacturing, Quality Control, and Document Control, to determine events (errors, deficiencies, discrepancies, deviations and other observations) and report to management. Manage a team of specialists to meet established targets. Manage and support review of batch related production documentation, ensuring resolution of all ident

CDP Solutions works throughout the United States with vertically integrated metal mills, service centers, distributors, extruders, fabricators, roll formers, CNC Shops and a wide variety of other metal fabrication companies. Responsibilities: Oversee the facility ISO 9001 Quality program. If you have a background in other quality systems such as ISO 13485, AS9100 or IATF 16949 that is a plus but not necessary. Manage the quality department’s KPI & report weekly & monthly to the executive leadership team. Oversee the calibration of all measurement tools. Provide coaching and training to operators and shop floor employees. Manage the corrective action and nonconformance processes. Review and implement quality and inspection systems and processes. Interact with customers from time to time. Oversee daily quality control activities within the manufacturing plant. Work with the engineering department when new products are introduced to the plant floor. Compensation Salary $100,000 - $120,000

Manager, Quality, Release (Tuesday to Saturday, night shift) Direct Hire Salary Range: $120-140k base Onsite in Philadelphia, PA Must be a US Citizen Must have experience managing direct reports Must have biopharma industry experience Shift: Tuesday to Saturday from 11PM to 7:30AM (Night Shift) We are seeking highly motivated Manager, Quality Release, to join the facility’s Quality Operations team. The Quality Operations team will be responsible for ensuring that all operations at the facility comply with cGMP regulations, as well as internal policies and procedures. The Manager, Quality Release will work alongside manufacturing, QC, and Supply Chain, helping to ensure that the highest standard of work is performed. Essential Functions and Responsibilities Ensure compliance to cGMPs and facility procedures. Interface with functional groups, such as Manufacturing, Quality Control, and Document Control, to determine events (errors, deficiencies, discrepancies, deviations and other observ