Qc Salary at Amtranet Group BETA

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

Location District of Columbia Description Cube Root Corporation is a Certified Disadvantaged Business Enterprise (DBE), a Minority Business Enterprise (MBE) and certified 8 (a) small business headquartered in the heart of Washington, DC. We specialize in construction management, program and project planning, project management, program management, facilities management and engineering services. Our passion is to provide professional advice to policy makers, developers, fellow engineers and others in the facilities planning, design and construction. As a company and as individuals, we are committed to the highest ethical standards and hold ourselves accountable to our clients, but most importantly to the communities, that depend on our work. We take on big challenges and are committed to seeing them through to a successful conclusion. We are also proud of our commitment to expand opportunities for people in underrepresented communities. The major duties and responsibilities of the QA/QC

At District Photo, our employees are the heart of our company. We are seeking Auditor in our Beltsville factory Job Overview Responsibilities Primary Responsibilities: Implement and maintain quality control processes throughout the print production workflow. Conduct regular inspections and audits to identify and address any deviations from quality standards and standard operating procedures across all stages and components of a production line. Verify that each process within a line is following Standard Operating Procedure, materials handling, and producing the best quality possible Monitor and correct behaviors that are contrary to SOP. Conduct regular inspections of incoming materials. Verify raw materials are to specifications and ready to be used in order assembly Collaborate with production teams to continuously improve quality metrics and reduce defects. Investigate and resolve quality issues, implementing corrective and preventive actions. Evaluate and plot device control tests

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

Job Type Full-time Description As a Director, Quality Control (Chantilly, VA) at Granules Pharmceuticals Inc, you wil lbe responsible for Directing and managing all facets of the Quality Control Lab, including samples, reference standards, supply/equipment, QC data trending analysis in compliance with cGMP/ICH and pharmaceutical regulatory compliance; Responsibilities include: Represent QC department during scientific and technical discussions with clients, vendors, and FDA representatives; Build and implement effective laboratory systems, processes, and teams for smooth lab operation using QC Validations; Oversee Quality Control Laboratory to ensure accurate ad tnalytical chemical testing results, adherence to company protocols, animely completion of projects using HPLC-UV, GC, IQ/OQ/PQ, STPs; Interface with different departments regarding quality issues, audits, and special projects; Provide guidance to pharmaceutical manufacturing regarding quality and cGMP issues to ensure complian

Immediate need for a talented QC Information Systems (QCIS) Specialist. This is a 12+ months contract opportunity with long-term potential and is located in Fredrick, MD(Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID: 25-67024 Pay Range: $35 - $40/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: Manager In-Take Notes: Exp with computer information systems Exp with data integrity Exp with GMP Understanding data management Previous lab experience Working Hours- M-F 8am-4pm or 9am-5pm Perform day-to-day activities and application administration of lab and manufacturing quality control computerized systems. Support QC lab functions, providing solutions to a variety of technical problems. Participate in software/computer system validation, IT for software/computer applications and fulfill all networking a

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

Position Overview: This position is a key member of the Elutia team and as such is involved in setting the Company’s short to medium range goals and objectives as it relates to quality assurance. The Manager of Quality Assurance & Quality Control is responsible for overseeing and maintaining the Elutia quality system and process compliance activities, on a daily basis including the monitoring of inspectional activities and dispositioning of non-conforming products. Interacts directly with internal and external customers on product release activities as needed. In addition, this individual will play an integral role in coordinating activities across departments to achieve desired growth and establish corporate goals in an entrepreneurial environment. For example, this leader will partner with operations to ensure compliance with applicable procedures. This position will be located on-site in the Company’s Gaithersburg, MD facility. Essential Duties & Responsibilities: • Review and appro