qa documentation specialist

Job Description We’re hiring a QA Documentation Specialist for our Northwest Houston client! We are looking for experienced, reliable, hard-working employees who can interview immediately! DESCRIPTION OF YOUR DREAM JOB: Job Title: QA Documentation SpecialistLocation: 77008Pay: $20.00/hourHours: Monday–Friday, 8:00 AM–5:00 PMDuration:...

QA Documentation Specialist Location: San Diego, CAType: Full TimeIndustry: Pharmaceutical ManufacturingPosition OverviewOur client is seeking a QA Documentation Specialist to support the development, revision, and review of GMP manufacturing documentation. The ideal candidate will have pharmaceutical or life-sciences experience and a strong...

Job Description: The QA Engineer is responsible for ensuring timely development, review, and approval of engineering, validation, and lifecycle documentation in alignment with corporate procedures, SOPs, cGMP, and industry best practices. This role supports manufacturing, engineering, validation, and quality teams by providing oversight across the full...

Job Title: QA Documentation Specialist Job ID: 26-02786 Location: Vacaville, CA Duration: 6 Months M-F 5x onsite 1st shift (8 am - 5 pm) Description We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System...

Job Title: QA Documentation Specialist I Job Duration: 6 months (onsite) Job Location: Vacaville, CA. 1st shift: M-F (8am - 5pm) Job Description: We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process...

Company DescriptionIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide...

Job DescriptionProcesses IT controlled documents such as computer system procedures, forms, specifications and test documentation in the Electronic Document Management System (EDMS) following defined processes/procedures. Scans, verifies and archives IT records in accordance with record retention requirements. Ensures the consistent application of Good...

M-F 5x onsite 1st shift (8am - 5pm) We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements. Key...

Summary: The QA Specialist primary responsibility is the review and approval GMP documentation associated with Site operations, to include Manufacturing, Validation, MES, and Quality Control. This role is to serve as a Subject Matter Expert (SME) for QA document review relevant to Equipment/Instrumentation, Validation Maintenance, and relevant...

About Bluu, Inc.Bluu, Inc. is a technology and payments company providing integrated POS, payment processing, hardware, software, online ordering, and business management solutions for the restaurant and retail industries.We are committed to delivering reliable, innovative technology that helps businesses operate more efficiently and grow. Join our team and...

Role: QA Documentation Specialist 2 Location: 101 International Drive, Portsmouth, NH 03801 Contract: 6+ Months – Possibility for Extension or FTE Conversion Pay Rate: $ 76.64/hr   Job Description Summary The QA Specialist primary responsibility is the review and approval GMP documentation associated with Site operations, to include Manufacturing,...

**Job Description** The QA Engineer is responsible for ensuring timely development, review, and approval of engineering, validation, and lifecycle documentation in alignment with corporate procedures, SOPs, cGMP, and industry best practices. This role supports manufacturing, engineering, validation, and quality teams by providing oversight across the full...

**QA Document Coordinator** **Job Type:** Contract **Education:** Associate’s Degree Required Job Summary We are seeking a detail-oriented **QA Document Coordinator** to support document control and administrative activities within a regulated GMP environment. This role will be responsible for maintaining accurate document tracking, scanning and...

At doTERRA we encourage all employees to seek out opportunities that will expand their skill set. We strive to help achieve personal career goals by providing opportunities of growth and movement throughout the company.Job Description: This position assists in technical documentation management regarding instructional documents in compliance with...

This position is responsible for coordinating the day-to-day documentation requirements of the Quality Department, reporting directly to the Quality Manager. Review and verifies document records to ensure documentation complies with regulations and internal quality control practices. Assists the Quality Manager to ensure that products produced meet the...

Description "All candidates must be directly contracted by ASK Consulting on their payroll and cannot be subcontracted. We are unable to provide sponsorship at this moment". Job Title: QA Documentation Specialist I Location: Vacaville, CA 95688 Contract: 06 months Pay rate: $26/hr on W2 M-F 5x onsite 1st shift (8am - 5pm) Job Description: We...

Quality Assurance Document Control Associate Specialist The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting. Primary responsibilities include:...

Quality Assurance Document Control Associate Specialist The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for Client Jump site records management. Responsibilities include but are not limited to receiving and reconciliation of GMP records, management of scanning, archival and retention of GMP...

Job Title: QA Specialist III ID: 26-04286 Location: Portsmouth, NH Duration: 08 Months Summary The QA Specialist primary responsibility is the review and approval GMP documentation associated with Site operations, to include Manufacturing, Validation, MES, and Quality Control. This role is to serve as a Subject Matter Expert (SME) for QA...

Job Title: QA Documentation Specialist 2 Job Location:Portsmouth, NH Job Duration: 9 Months on W2 Job Summary: The QA Specialist primary responsibility is the review and approval GMP documentation associated with Site operations, to include Manufacturing, Validation, MES, and Quality Control. This role is to serve as a Subject Matter Expert (SME) for...