Manager, Quality Assurance Salary at Fujirebio Diagnostics Inc BETA

Quality Assurance Manager - $100k - $120k Richboro, PA US Citizens or GC holders only No C2C Could you be my clients next Quality Assurance Manager? Leading their manufacturing quality team and ensure that all parts of the manufacturing process meet strict specifications. In this leadership role, you will be responsible for developing, managing, implementing, and continuously improving Quality Management Systems and processes. Your contribution will play a crucial role in advancing the company's position within the industry. Key Responsibilities: Oversee the daily operations of the Quality Department to meet set goals and objectives. Serve as the primary quality representative for existing and new products, leading and developing all aspects of Quality Assurance within manufacturing processes. Review and approve quality documentation, including validation reports, product test protocols, change management, CAPA, customer complaints, and audits. Develop and manage policies, procedures,

Job Description Job Description The QA Manager primarily works across teams to ensure that software systems and components are successfully integrated across hardware systems and meet specified requirements. Will be primarily responsible for testing products and software to ensure quality and a successful rollout. Will also assist in managing one additional scrum team. Participates and leads the defect triage process which includes identifying, reproducing, and documents defects, bugs, or problems and helps lead the teams on scrum ceremonies. Core Responsibilities • Take leadership and manage multiple scrum/application teams across tasks • Take proactive leadership across multiple applications/initiatives • Design and develop QA/Test solutions based on available requirements even if they are not completely defined to keep making progress in a timely manner. • Create Test Strategy across larger initiative. Present test strategy across scope, environment, data and other dependencies acro

**_What Nuclear Manufacturing contributes to Cardinal Health_** **Manufacturing** is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. **Nuclear Manufacturing** is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. **Schedule** : + 40 Hours per week + Monday Friday - Must be willing to work any 8hr shift between 9pm - 4am (first shift comes in at 8pm and last shift comes in at 4am on average). + Must be willing to work weekends as part of a rotation, and holidays are contingent upon customer demands + Candidate must be flexible to work different shifts, schedules, days and overtime as needed. **_Responsibilities_** + Successfully complete extensive training, includi

At Universal Pure, we’re dedicated to giving people everywhere safe, fresh, and delicious food to eat and drink. We provide high-pressure processing (HPP), value-added services and cold storage for our partners in the food industry. We are focused on safety and driven by service. Quality Assurance Supervisor Position Summary: The Quality Assurance Supervisor is the food safety coordinator and quality advocate for the assigned facility. Key drivers are supporting the quality control function within the company while ensuring policies like Good Manufacturing Practices (GMPs) and Standard Operating Procedures (SOP) are executed. The position requires knowledge of quality methods, techniques, and equipment. The QA Supervisor must have or achieve within a reasonable timeframe certification in SQF, HACCP, and PCQI. The role reports to the Regional Quality Assurance Manager. This position has 4-5 direct reports that compromise hourly 3-4 QA Techs and 1 Sanitation rep. Typical Hours between 7:

Join Kelly FSP as an Operations Scheduler at our Client Site in West Point, PA! Job Title: Operations Scheduler Summary: You will be responsible for overseeing internal stakeholder relationships, providing guidance to ensure compliance with required regulations. Maintain the Master Schedule for site visibility to future orders, site capacity and utilization Provide input for label room production schedules across all shifts Hold frequent meetings to gather details from internal teams and communicate status of orders Aid in answering internal team questions as it relates to planning of the daily, weekly, and/or future production schedules This role will work with internal business partners, technical leaders, and subject matter experts to ensure all issues are escalated and that data-driven decisions are made to ensure timelines are met Responsibilities Supplement and maintain detailed Master Project Schedules as serve as backup to lead scheduler. Work closely with production managers,

Summary The Manager, Quality Operations is responsible for managing quality operations functions within the respective manufacturing facility. Responsible for ensuring compliance with the applicable regulations of all countries in manufacturing and distributing products based on Quality System Regulation, and the Medical Device Directive. Responsibilities Establish and promote a work environment that supports compliance with the Quality System and company policies. Support the development of efficient and effective methods for meeting Quality System requirements. Prepare, communicate, and evaluate team goals and objectives for continual improvement of the quality system. Ensure linkage to Strategic Quality Plan. Manage a team of Quality Engineers in driving robust problem solving, NC reduction and continual improvement efforts. Drive values stream optimization through the application of proven methodologies such as Six Sigma, LEAN, Kaizen events etc. Promote production line value strea

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

Overview: The Area Manager has direct supervisory and financial responsibility for East Region Power Substation BU. This business unit performs power work across the East Region territory. Duties include overall management, oversight of all construction related activities and personnel assigned to the BU, development and implementation of resource and production plans to meet customer needs. The Area Manager completely understands the business, the context, and manages implications related to the East Region Power Substation BU activities. The Area Manager develops business relationships with customers, subcontractors, vendors, and industry associations, while also maintaining relations with local trade unions regarding labor management and grievance resolution within the Area. This role is responsible for compliance with H&M safety policies and procedures, assists in the investigation of incidents and claims, and communicates lessons learned to crews. This position may require travel