qa document control specialist

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...

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 is a 100% onsite position. Description Details General Position Summary/Purpose: Assists in maintaining a compliant, efficient Quality Assurance Document Management program. Key Accountabilities/Core Job Responsibilities: Under direct supervision, perform day-to-day Document Control activities: Process DCR packages and review for correctness and...

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...

Join our team as a QA/QC Document Control Specialist, where you will play a crucial role in ensuring the accuracy and integrity of our documentation processes. You will be responsible for managing, organizing, and maintaining quality assurance and quality control documents, ensuring compliance with industry standa...

Position Summary: As the QA Document Control Associate, you will support Quality Assurance (QA) activities. Activities include but are not limited to: Maintenance and organization of the Central File system, Issuance of documents, Review and Release of Batch Records, and Support of MasterControl tasks (such as Document Collaborations). All in accordance with...

Company DescriptionValidation & Engineering Group, Inc. is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, among other services.Job DescriptionDocument Control / Data...

Overall responsibility: This position is responsible for tracking, maintaining, and archiving all GMP documentation in compliance with FDA regulatory requirements as well as company procedures and policies. - Ensuring effective management of SOPs, master records, component documents and manufacturing batch records  - Issuing and distributing...

Enter Job Description... Ensures effective control, accuracy, and compliance of quality documentation within the Quality Management System (QMS) by managing document lifecycle processes, including document review, approval, version control, document inventory management, archival and retrieval, and periodic documentation verification activities. Key...

Company DescriptionProgressive GEJob DescriptionProvide project document control of a Combined Cycle Project’s Architectural Engineer, Owners Engineer, Contractors and other drawings, documents, records as well as perform other administrative duties as directed.QualificationsRequirements:• Ability to work independently and be self-directed; Possess...

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...

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...

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 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 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...

Revolution Medicines is a global, commercial-state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target...

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...