QA Specialist III Salary at Curia Inc BETA

Company Profile SepsaMedha North America is located in Ballston Spa, NY and manufactures power supplies, converters and passenger information and onboard systems for rail vehicles. SepsaMedha is a benchmark in the industry with more than 30,500 converters and 35,000 on-board systems installed in the trains of the main manufacturers in more than 30 countries. Today, as part of the MEDHA group, we continue to provide our customers with the talent and human value of our team, which is, without a doubt, our greatest strength and differentiation. Position Summary The Senior Quality Assurance Specialist will serve as the primary Quality point of contact for Kawasaki, focusing on the R211 project while ensuring compliance with all applicable quality standards and customer requirements. This role requires expertise in quality management systems, ISO certification, supplier evaluations, non-conformance management, and audit processes. The position will work closely with internal Quality team me

Position overview The Quality Assurance (QA) Specialist I is responsible for maintaining Quality databases and providing an on-the-floor QA presence and oversight to manufacturing operations. This positions role will include identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action such that a) adherence to cGMPs and internal procedures/policies are maintained, and b) appropriate immediate corrective action is implemented and effectively documented in order to provide traceability and substantiation of any claims to be made in the investigation. This position primarily works in the cGMP production areas to manage adherence to the quality system and to initiate and assist in the initiation and resolution of deviations. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the know

Job Description QUALITY ASSURANCE SPECIALIST III (Analytical Labs) in Albany, NY CURIA provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. We are seeking a highly skilled and experienced Quality Assurance Specialist III (Analytical Labs) to join our Quality team. The ideal candidate will be responsible for technical data review to ensure accuracy and integrity, overseeing the implementation of new test methods, and conducting internal audits to maintain compliance with cGMP and SOP requirements. The successful candidate will possess strong communication, problem-solving, and technical skills, with proficiency in analytical instrumentation such as XRPD, PSD, DSC, HPLC, GC, NMR, and ICP-MS. This role serves as a subject matter expert (SME) in managing deviations, OOS/OOT/COOT incidents, complaints, and change controls within our analytical labs, ensuring timely and compliant resolutions. Key responsibilities include supporting

Job Title: QA IT Validation Specialist Location: Albany, NY Job Summary: We are seeking a skilled QAIT Validation Specialist to support IT Quality and Data Integrity initiatives within a regulated environment. This role acts as a Subject Matter Expert (SME) in supporting investigations, risk assessments, and IT operations, ensuring GxP computerized systems continue to operate as intended post-validation. The consultant will work cross-functionally to help develop and enforce policies that ensure compliance with regulatory standards. Key Responsibilities: Collaborate with IT teams to ensure compliance with internal Quality System requirements. Apply Quality Risk Management (QRM) principles in both formal and informal assessments. Support and guide activities related to change controls, CAPAs, deviations, audits, SOPs, and data integrity. Assist with internal/external IT audits and support vendor qualification efforts. Contribute to Quality Assurance Agreements (QAAs) and Approved Suppli

**_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

**_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. Cardinal Health Positron Emission Tomography (PET) Manufacturing Services is responsible for manufacturing PET radiopharmaceuticals to enhance patient treatment through improved disease diagnosis, staging, and monitoring. **_Responsibilities_** + Supports an effective Sponsor training program. + Ensures Sponsor documentation is curr

Overview: Pay Range: $17.00 - $21.00 per hour SCOPE: Under direct supervision, is responsible for the collecting and processing of specimens form patients, documenting results according to established procedures. Assists with performing specimen analysis, instrument maintenance, and quality control procedures as indicated. Follows quality assurance and safety policies and procedures. Assists with patient flow as needed. Supports and adheres to the US Oncology Compliance Program, to include the Code of Ethics and Business Standards. Responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES: Collects appropriate specimens from patients as ordered. Maintains proper documentation as described by the quality assurance program including accessioning logs, test report logs, quality control logs, equipment records and checklists. Performs specimen analysis of all chemistry, hematology, immunology specimens as directed. Maintains adequate inventory of supplies and ensures that all supplies are vi

Job Description Environmental Technician - Asbestos Project Monitor - Latham, New York Intertek, a leading provider of quality and safety solutions to many of the world's top-recognized brands and companies, is actively seeking an Environmental Technician to join our Environmental team in Latham, New York. This is a fantastic opportunity to grow a versatile career in the environmental industry! Intertek's Building and Construction division is a suite of Intertek brands that are industry leaders across multiple architecture, engineering and construction disciplines, developing the most innovative product and project solutions. Intertek's project-related assurance, testing, inspection and consulting services are the risk management and quality assurance partner you need to ensure the reliability, safety and performance of your new developments, existing assets and facilities. Professional Service Industries, Inc. (Intertek-PSI) is a leading US based provider of construction assurance, te