Qc Salary at The Irex BETA

Job Description Job Description Summary The Director of Quality provides technical support, manages quality control (QC) processes, ensures compliance with standards, oversees QC staffing, and drives continuous improvement initiatives across the Mid-Atlantic Region and beyond. This role is key to maintaining the teams high-quality standards and supporting project teams through proactive planning, audits, and training. Roles and Responsibilities The Director of Quality will perform the following duties in a safe, productive, and effective manner: Provides preconstruction, operational and regional support Manages regional QA/QC program standards Manages QC startup process and QC inspector team Performs monthly project audits and check -ins Manages pour card process regionally Manages/Works with project teams for QC-related situations Performs quality-related training support Develops best practices Develops and update OPS report library Participates in training and certifications Require

Overview At Bohler, we empower the ambitious to become the accomplished . We are looking for dependable, responsible, and detail-oriented Quality Control Engineer to join our Mid-Atlantic team. Our Mid-Atlantic offices are looking for a Quality Control Engineer who embodies this purpose. Responsibilities What Youll Do: + Provide high-level strategy for unique design projects + Internal Quality Assurance / Quality Control aspects during the project design and construction process + Ensure compliance with all internal Quality Control processes + Completion of Quality Checklists for design + Review of all site safety design features + Detailing consistency + Constructability review + Assessment / improvement / maintenance of QA/QC procedures + Construction Administration + Assist design team in support of Construction Administration services for design projects What We Offer: + A supportive and flexible work environment that empowers employees to stay healthy, fulfill their passions, and

Overview: At Bohler, we empower the ambitious to become the accomplished. We are looking for dependable, responsible, and detail-oriented Quality Control Engineer to join our Mid-Atlantic team. Our Mid-Atlantic offices are looking for a Quality Control Engineer who embodies this purpose. Responsibilities: What Youll Do: Provide high-level strategy for unique design projects Internal Quality Assurance / Quality Control aspects during the project design and construction process Ensure compliance with all internal Quality Control processes Completion of Quality Checklists for design Review of all site safety design features Detailing consistency Constructability review Assessment / improvement / maintenance of QA/QC procedures Construction Administration Assist design team in support of Construction Administration services for design projects What We Offer: A supportive and flexible work environment that empowers employees to stay healthy, fulfill their passions, and balance work and life

About APSI: Come join our family of dedicated professionals focused in our pursuit of excellence by providing an unparallel customer experience as we work to transform the built environment. Whether exceeding our clients ' expectations, working hard to exceed our industry's professional standards, discovering growth opportunities, or giving back to our communities, our people are the foundation of our success. Be a part of our collaborative, diverse, and dynamic team! Our excellent benefits package includes: Paid Holidays and Vacation Days Attractive Compensation Health Insurance (Medical/Dental/Vision) 100% Employer Paid Life/AD & D & Long-Term Disability Benefits 401k License & Certification Reimbursement Program Employee Referral Program Role: QA/QC Inspector (Mechanical Experience) Location: Woodlawn, MD (ON-SITE) Salary: $90,000-$94,000 Client: GSA Project: Social Security Administration Headquarters - Altmeyer Column Repair Duration: 2+ years + (additional 2+ years) Project Detai

Informazioni sulla location: Nello stabilimento di Paullo siamo in grado di sviluppare e produrre Principi Attivi Farmaceutici (API) generici e di marca e intermedi avanzati su scala commerciale. La nostra gamma di prodotti comprende oltre 80 API generici prodotti secondo gli standard di cGMP. Il sito produttivo ospita 350 dipendenti ca, organizzati in otto reparti dedicati a produzione farmaceutica, essiccamento, finitura e purificazione. Comprende inoltre un vasto impianto pilota e laboratori per lo sviluppo personalizzato e di analisi dei Principi Attivi, oltre ad uffici amministrativi, commerciali e di coordinamento delle Operations. Per maggiori informazioni http://www.cambrex.com/about Riassunto del lavoro: La risorsa operer allinterno del Team di Controllo Qualit di Cambrex Profarmaco Milano (40 FTE ca), a riporto diretto del QC Manager e avr le seguenti responsabilit: Compiti e responsabilit: Coordinamento dei Supervisori del gruppo QC, interfacciandosi con QC Manager e QC Plan

Your vision is ambitious. Just like ours. Our people are our success. As one of us, you will contribute to engineering excellence for the high-tech markets of the future, including semiconductors, batteries, pharmaceuticals, biotechnology, and data centers. At Exyte, you will be part of a global community of challenge seekers who are ambitious and passionate about innovation. Together, we will build on our company's long history and keep on leading the way to a better world. Discover your exciting role The QA/QC Inspector located in Malta, NY is responsible for inspections of installed or partially installed process piping systems, and monitors the handling of materials in compliance with the construction site / project quality assurance program. Explore your tasks and responsibilities Performs material inspection Performs weld inspection Performs installation inspections Conformance / non-conformance reporting Performs hydrostatic pressure test Performs pneumatic pressure test Perform

The **Sr. QC Scientist - Compliance** role is critical to our patients. This role is responsible for supporting compliance in the Quality Control Laboratory, including authoring, management and/or tracking of investigations/events/deviations, Corrective Action / Preventive Action (CAPA), change control, and other Quality records. This position will facilitate the compiling, trending, completing, and reporting of key quality metrics for management accountability, and other quality control functions, as needed. Continuously monitor systems, logbook management, and testing procedures to ensure compliance with applicable regulatory and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mis

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development. PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories. PDS is seeking a QC Document Reviewer I to join our team in Gaithersburg, MD. This position will be primarily responsible for reviewing all laboratory documents, records and logs for accuracy and adherence to analytical plans, methods, SOPs, GLP guidelines, and established laboratory policies. This position is performed under regular supervision. Salary for range for this position is $21.81- $26.65 per hour. Sala