6 results for Dqc jobs

QE temp

West Henrietta, NY
onsite
Temporary
17.5 - 17.5 USD / Hourly
We are looking for a detail-oriented individual to join our team as a QE contract employee in West Henrietta, New York. In this contract position, you will play a key role in assembling and preparing quarterly statement packages for delivery, ensuring they meet quality and production standards. This opportunity is ideal for someone with strong organizational skills and experience working with office equipment. Responsibilities: • Compile quarterly statement packages based on client-specific requirements and prepare them for delivery. • Ensure all packages include necessary documents such as tax notices, employee 1099 and W2 forms, and additional reports. • Operate and maintain office equipment including mail metering machines, PCs, label printers, and shipping tools. • Monitor production timelines and adhere to quality standards to ensure timely delivery. • Organize and track packages to ensure accuracy and efficient processing. • Collaborate with team members to improve workflow and maintain high service levels. • Address any issues with equipment or packaging processes promptly to avoid delays. • Perform regular quality checks on assembled packages to ensure completeness and accuracy. • Maintain accurate records of processed packages and delivery schedules. • Assist in troubleshooting and resolving operational challenges during peak periods.
2026-03-13T00:00:00Z

Quality Control Coordinator

Branford, CT
onsite
Temporary
18 - 20 USD / Hourly
Responsibilities: • Quality Admin Support will be responsible for administrative tasks supporting the complaint handling process such as data entry on the computer, organizing electronic files, filing documents, scanning, printing, and organizing folders. Qualification: • Proficient in using Microsoft Office Suite (Word, Outlook); basic Excel skills. • Experience with document scanning equipment and PDF software (e.g., Adobe Acrobat). • Ability to organize and maintain electronic filing systems and folders on shared drives. • Basic knowledge of data entry and file naming conventions. • Strong attention to detail and accuracy in labeling, sorting, and archiving documents. • Excellent time management skills to handle multiple filing and scanning tasks efficiently. _____________________________________________________________________________________________________________________________________________ • This role is basic clerical, so we anticipate the bill rate to be comparable to the prior temps/candidates that we had. Pay rate to temp, entry level is $18 an hour • They will be trained by 2 team members / very friendly and welcoming / excited about having an extra pair of hands! • Currently no opportunity to convert to perm however we often find a place for hardworking folks / no guarantees though • Preferred hours are: 8am - 4pm / but open to 6am - 2pm, 7am - 3pm • Located at our Branford manufacturing site (clean, quiet, more of an assembly site) • Easy and convenient free parking right outside the building / one story building / easy access • Free lunch every other Wednesday / monthly ice cream parties / fresh fruit supplied / modern, recently installed large kitchen, break room • Great culture / friendly, inclusive atmosphere • Attention to detail very important • Based at 14 Commercial Street in Branford / right off Route 1 / exit 56 off 95 / business park located behind the Parthenon Diner • Interview process: Dawn phone screen / then on-site interview with hiring manager and two other team members
2026-03-09T00:00:00Z

QA Lead

Cincinnati, OH
remote
Temporary
61.75 - 71.5 USD / Hourly
We are looking for an experienced QA Lead to join our team in Cincinnati, Ohio. In this long-term contract position, you will be responsible for overseeing quality assurance processes and driving data analysis initiatives to support fraud prevention efforts. This role requires a detail-oriented individual with expertise in fraud analytics and investigative techniques. Responsibilities: • Lead quality assurance processes to ensure systems and data meet organizational standards. • Conduct in-depth data analysis to identify trends and anomalies related to suspected fraud. • Develop and implement fraud prevention strategies tailored to organizational needs. • Collaborate with cross-functional teams to enhance fraud investigation processes. • Utilize advanced analytics tools to support anti-fraud measures. • Monitor and refine workflows to improve efficiency in fraud detection efforts. • Provide detailed reports and insights on fraud-related activities to stakeholders. • Train and mentor team members on best practices in fraud analytics and investigation. • Stay updated on industry trends and emerging threats in fraud prevention.
2026-03-13T00:00:00Z

USA - Engineer I - CTQ

Skaneateles Falls, NY
onsite
Temporary
23 - 27 USD / Hourly
Software Test Engineer (Onsite – Medical Device Project)Location: Skaneateles, NY (Onsite; minimum 3 days/week, fully onsite strongly preferred)Pay: Available on W2 Employment Type: 40 Week Contract OverviewWe are seeking a Software Test Engineer to support a short‑term project involving manual testing of a legacy medical device. This role focuses on validating software functionality for a camera-based device used in pediatric vision assessments. The position is primarily manual/black‑box testing with hands-on interaction with the device, its UI, and simple networking components.Key Responsibilities<ul><li>Design and update test protocols based on design modifications and software requirements.</li><li>Execute test plans covering functional, integration, system, and performance testing.</li><li>Gather evidence to validate software behavior and confirm it meets specified requirements.</li><li>Identify, document, and track software defects and inconsistencies; collaborate with engineering teams to reproduce and troubleshoot issues.</li><li>Work closely with cross‑functional partners including software engineers, the test manager, design assurance, and product stakeholders.</li><li>Create and maintain clear and organized test documentation, including test cases, test plans, test reports, and defect logs.</li><li>Set up and use small contained networks for device testing.</li><li>Connect the device to printers and basic web services for data upload/download scenarios.</li><li>Operate the device’s touchscreen interface and follow detailed manual test steps.</li><li>Occasionally interact with electro‑mechanical components as part of the testing process.</li></ul>
2026-03-11T00:00:00Z

Quality Director

Dallas, TX
onsite
Permanent
150000 - 160000 USD / Yearly
We are looking for an experienced Quality Director to lead and manage the Quality Unit in a sterile drug manufacturing environment. This role involves ensuring compliance with regulatory standards, overseeing quality operations, and serving as the primary expert in aseptic manufacturing and pharmaceutical distribution. The ideal candidate will bring strategic leadership and technical expertise to maintain high-quality standards and regulatory adherence. Responsibilities: • Lead the Quality Unit to ensure compliance with all regulatory standards for 503B Outsourcing Facilities and sterile drug manufacturing. • Oversee quality operations, including aseptic manufacturing processes and wholesale pharmaceutical distribution. • Represent the organization during audits and inspections conducted by regulatory agencies and third-party auditors. • Manage documentation processes, including batch records, ensuring compliance with cGMP and aseptic protocols. • Develop and implement quality systems for deviation management, change control, investigations, and product recalls. • Approve validation protocols, qualification reports, and standard operating procedures to meet regulatory requirements. • Ensure adherence to guidelines for handling hazardous drugs and sterile preparations. • Maintain compliance with state and federal regulations governing wholesale drug distribution. • Drive continuous quality improvement initiatives and risk management strategies. • Provide technical expertise and leadership in sterile manufacturing and quality assurance practices.
2026-03-13T00:00:00Z

Quality Assurance Coordinator

Chatsworth, CA
onsite
Permanent
70000 - 90000 USD / Yearly
Quality Assurance CoordinatorIndustry: ManufacturingCompensation: $70K - $90K + benefitsLocation: Hybrid 3x onsite in Los Angeles, CA required. approximately 10% international travel requiredNice to have: Bilingual in Spanish/English We are looking for a Quality Assurance Coordinator to join our team in Los Angeles, California. In this role, you will oversee strategic quality assurance processes and collaborate with global teams to ensure compliance with industry standards. This position offers the opportunity to lead quality systems development and grow into a leadership role within the organization. Responsibilities:• Conduct inspections of incoming goods to ensure compliance with quality standards.• Manage supplier quality by maintaining strong relationships and monitoring their performance.• Perform factory audits and inspections to verify adherence to established processes and procedures.• Develop, implement, and maintain systems that comply with ISO standards and other applicable regulations.• Collaborate with global teams to enhance quality assurance practices across production facilities.• Travel to international production sites approximately every five weeks to oversee quality processes.• Work closely with sourcing, production, and compliance teams to ensure operational efficiency.• Assist in building and improving quality control systems within the organization.• Provide strategic input to align quality assurance processes with organizational goals.• Support the growth and development of the Quality Control team, fostering leadership potential
2026-03-04T00:00:00Z