Manager, Quality Salary at Duhadaway Tool BETA

Full-time Quality Manager * Newly opened hospital! * Medical/Dental/Vision, 401k, PTO, and more! About Haven Behavioral Hospital of West Chester Haven Behavioral Hospital of West Chester is a 72-bed facility providing high-quality, specialty behavioral health services for individuals with mental health and substance abuse issues. Our success is a reflection of the excellence and dedication of our employees at every level of our facility. The culture of our hospital is built around service. All jobs performed on our team are worthwhile and every employee makes a difference. If you are looking for an opportunity to grow personally and professionally while delivering compassionate, quality care we encourage you to explore career opportunities with Haven of West Chester. Position Summary: Supports the Performance Improvement & Risk Management Department in the management of performance improvement, educational development and policy oversight performance measures. Collaborates with multi-d

Description Is Kymanox the right fit for you? You want to make a difference and have an impact... You enjoy having an influence in your day-to-day work... You are motivated by working alongside a team filled with subject matter experts who will help you learn and grow... You wake up every day and do what you do ... because patients deserve better. If this sounds like you, you've come to the right place. The Manufacturing Quality Specialist will join our Quality Assurance and Compliance team and play a key role in providing quality support for the King of Prussia small-scale device manufacturing facility and process development. The specialist would also support Kymanox's clients with compliance activities, with an emphasis on quality oversight of contract manufacturers and batch production, gap assessments, and phase-appropriate quality management system implementation. Responsibilities: Quality support of daily operations of early-phase or design phase device subassembly manufacturing

Job Description Job Description Production Technician- HPLC Columns This position is a full-time Non-exempt position located on site in Newark, DE. Check us out on the web! https://www.sepax-tech.com/employment.php Position Summary: This individual must be a self-motivated, detail oriented and energetic person with some chemistry background. The individual must be a quick learner with a mechanical/problem-solving mind to properly produce columns that meet production quota and standards to qualify for the monthly production award program. This full-time non-exempt position is based at our headquarter office located in Newark, Delaware. Requirements: High school graduate with 2+ years of industrial lab experience or associate degree in a science field. Good understanding of general separation science. Be able to strictly follow the Standard Operating Procedures. Proficient computer skills to utilize Microsoft software and an ERP system for day-to-day departmental operations. Well organiz

Title: Production Manager Report: VP of Supply Chain Location: Newark, DE Position Type: Full Time, Exempt Travel: Occasional About AirJoule, LLC Are you passionate about making a difference in the fight against climate change? Then AirJoule is the place for you! We are a joint venture between GE Vernova and AirJoule Technologies (formerly Montana Technologies), and a leader in the global sustainability transition. Our revolutionary atmosphere water harvesting technology enables transformative HVAC products that help our customers save money on their energy bills while reducing their environmental impact. The same core technology also enables atmospheric water harvesting products that create clean, abundant, and decentralized water for industrial, commercial, and humanitarian purposes. If you are a highly motivated and experienced individual who wants to make a real-world impact, we encourage you to apply! Position Summary AirJoule is seeking a highly motivated and experienced Producti

Quality R&D Lead - Contract - Collegeville PA Proclinical is seeking a Quality Integration Specialist to support the assessment and integration of quality plans for external partners. Primary Responsibilities: This role focuses on developing third-party quality strategies and ensuring compliance with data integrity, GxP regulations, and national health authority requirements. You will play a key role in promoting a culture of quality and safety while providing GMP expertise and regulatory compliance advice. Skills & Requirements: Understanding of GMP and project management skills. Experience in risk management and manufacturing processes. Problem-solving abilities and excellent communication skills. The Quality R&D Lead's responsibilities will be: Assess the quality posture of external partners to identify risks and improvement needs. Oversee operational quality activities, including deviations, change controls, CAPAs, and batch release for drug substances and products. Manage project

**The Opportunity** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. + Reporting compliance status data to operational quality management + Collaborate with center management in the development and implementation of continuous improvement plans + Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns + Responsible for coordinating and managing training activities, policies and processes at the center level. You will report to the Assi

**The Opportunity** This position provides immediate support to the Assistant Manager of Quality in monitoring plasma center processes to ensure overall compliance with CSL Operating Procedures, as well as all applicable local, state, federal requirements. This role will ensure compliance to training needs, SOPs, processes and other regulatory or company directives are adhered in order to support the operations and quality requirements for business operations. + Reporting compliance status data to operational quality management + Collaborate with center management in the development and implementation of continuous improvement plans + Collaborate with Assistant Manager of Quality (AMQ), to be able to represent the center during internal and external audits, responds to questions, and may stop operations, including shipments to address quality concerns + Responsible for coordinating and managing training activities, policies and processes at the center level. You will report to the Assi

**_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