Supervisor, QC Salary at Data Matique BETA

We are looking for the right people - people who want to innovate, achieve, grow and lead. We attract and retain the best talent by investing in our employees and empowering them to develop themselves and their careers. Experience the challenges, rewards and opportunity of working for one of the world's largest providers of products and services to the global energy industry. Job Duties and Qualifications * Plans, reviews, and analyzes quality related data. Identifies problems, offers resolutions, and performs reporting activities. * Conducts statistical studies using Statistical Process Controls and other Quality Improvement Process tools. * May implement a Quality Assurance and/or Quality Management System such as ISO 9000, API, ASME, etc. for the site or project. * May act in vendor surveillance activities on projects. Requirements: * High school diploma or equivalent is required. Candidates having qualifications that exceed the minimum job requirements will receive consideration fo

Job Description Job Description Job&Talent is seeking an On-Site Manager for the world-class UPS Mail Innovations in Carrollton, TX. Join a great team and be rewarded for your hard work! Pay and Hours: $70,000 - $80,000 Shift: 5/6 AM - Finish Monday - Saturday. Flexible based on mail volume. Job Description: Must have warehouse management experience Anticipating staffing requirements and client expectations. Providing productivity, headcount, attendance, and other reports at the client’s request. Managing employee relations at the site – including coaching, counseling, performance reviews, removal from assignments, and exit interviews. Ensuring the warehouse floor is properly staffed and operated. Responsible for Fill Rate/Cost Per Piece/Miss Sorts/On Time Attendance. Documenting terminations for unemployment purposes Proactively communicating staffing needs to NRC Developing contingency plans for unexpected events. Ensuring On-Site Coordinator duties are performed to standards. Respon

Job Description Job Description Position Summary: The QC Associate works as part of a collaborative team following procedures already in place to sample all materials that are used to manufacture and pack products at the facility. The QC Associate will demonstrate attention to detail, and proper procedures while assisting and supporting the laboratory and production needs. The QC Associate will be required to record data in documentation with accurate and legible entries following GMP. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform the following satisfactorily; other duties may be assigned as needed. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. · Have knowledge of SQF or other food safety regulations · Read and comprehend SOP’s (Standard Operating Procedures) · Move materials from Receiving to Quarantine Area for review prior to releasing. · Sample raw ma

**Research Assistant III** **Dallas, TX** **Schedule: M-F 8a- 5p (some weekend and Holidays depending on process)** The cGMP QC Technician reports to the cGMP Manager, and the QC Supervisor. Once fully trained, this individual will have the ability to work independently while performing specialized techniques in an FDA-regulated cGMP Core Lab. The primary job will be reagent/supply ordering & test cellular based products for quality and ship investigational cellular products for therapeutic use in human phase I clinical trials The cGMP QC Technician assures all activities in the lab complies with Federal, State and local regulations and policies. **CORE FUNCTIONS Quality Control** Performs specialized quality tests on manufactured products for use in human phase I clinical trials. Performs new method development & qualification as needed. Creates SOPS, lab forms as needed. Assists in the release of manufactured products to clinic. Assists QC during environmental monitoring activities.

Company Overview Our client is a prominent and globally recognized company in the electronics contract manufacturing industry with a robust and well-established global presence, and a stablished reputation for operations excellence and highest customer satisfaction across continents. As part of their strategic expansion projections, they are actively seeking a highly accomplished Senior Operations Manager to guide their operation within the United States. Additional information will be given to qualified candidates. Additional information will be given to qualified candidates. Title: Senior Operations Manager (on-site role) Location: Dallas, Texas Reports to: Regional VP of Operations The Position Our confidential client is looking for an experienced Senior Operations Manager for a growing and leading company in its industry. This is an outstanding opportunity for an energetic and self-driven individual, able to perform in a highly complex and fast-paced environment and bring the opera

Job Duties and Qualifications Plans, reviews, and analyzes quality related data. Identifies problems, offers resolutions, and performs reporting activities. Conducts statistical studies using Statistical Process Controls and other Quality Improvement Coordinator, QC, QA, Senior, Manufacturing, Technology

**Roles: QA officer (Compliance & testing focus)** **Location: Jax/Dallas, TX (Hybrid - 3 days onsite per week)** **Position type: 15+ months with high possibility of extension/Conversion as FTE** **Pay range: $42 - $46/hr on W2 (All inclusive)** **Job Description:** The Quality Assurance Officer is a strategic professional who stays abreast of developments within own field and contributes to directional strategy by considering their application in own job and the business. Recognized technical authority for an area within the business. Requires basic commercial awareness. There are typically multiple people within the business that provide the same level of subject matter expertise. Developed communication and diplomacy skills are required to guide, influence and convince others, in particular colleagues in other areas and occasional external customers. Significant impact on the area through complex deliverables. Provides advice and counsel related to the technology or operations of t

Summary: Ability to inspect in process and finished products in the cleanroom environment. Act as coordinator within Quality Operations and ensure needs of internal customers are met. Document all non-conformances when necessary. Assist with investigations pertaining to, both, customer complaints and internal non-conformances. Understand, follow, and practice the rules/regulations set forth by the QSR, ISO 13485, and Quest Medical management. General Duties and Responsibilities: Review processes to assure procedural compliance and recommend improvements. Provide support during internal, customer and regulatory audits. Ability to identify key inspection points and the proper tools/equipment to ascertain these points. Perform inspections and verification of finished products. Perform Line clearance and in-process inspections. Review inspection data and DHRs (including sterilization records) for accuracy and compliance to the applicable standard(s). Perform inspections and process Returne