Manual QA Engineer Salary at Vrp Consulting Inc BETA

Field Materials is the leading AI platform to control and verify spending for the construction industry. Founded by serial entrepreneurs with exits to Fortune 500 companies (including Paypal), Field Materials has partnered with prominent VC funds in Silicon Valley to build a world class team with a bold vision to become the commerce and financial technology backbone of construction. This is a unique opportunity to join at the ground level an industry transforming company. Our company is the people we hire. We aspire to build a team of smart, high-caliber players that inspire each other to excel yet are not afraid to leave egos behind, roll up their sleeves and fix what doesn't work. We don't believe in micromanagement and trust our team to take full ownership of their responsibilities. We believe in transparency as a way to build trust, break communication barriers, and align towards a common goal. Finally, we want our people to stay and grow with the company and the only way to achiev

Exciting new contract with our key Biotech client in the Bay Area for an initial 6 month contract, with extension likely. Ideal candidate will be experienced with Veeva Systems and have previous experience in training the GxP Quality Systems... The Opportunity: Manage and maintain the GxP document control system, which includes product-related documentation, quality manuals, external documents, departmental procedures, and work instructions. Coordinate all aspects of incoming, in-process, and completed document change controls, ensuring supporting documentation is provided, changes are completed, and documentation is properly closed out and released. Oversee and maintain the GxP training program, including assigning training, archiving completed records, monitoring compliance, and conducting periodic audits of training records. Train new users on the document control and training systems, as needed. Provide guidance on document control practices and procedures to various departments. S

Exciting new contract with our key Biotech client in the Bay Area for an initial 6 month contract, with extension likely. Ideal candidate will be experienced with Veeva Systems and have previous experience in training the GxP Quality Systems... The Opportunity: Manage and maintain the GxP document control system, which includes product-related documentation, quality manuals, external documents, departmental procedures, and work instructions. Coordinate all aspects of incoming, in-process, and completed document change controls, ensuring supporting documentation is provided, changes are completed, and documentation is properly closed out and released. Oversee and maintain the GxP training program, including assigning training, archiving completed records, monitoring compliance, and conducting periodic audits of training records. Train new users on the document control and training systems, as needed. Provide guidance on document control practices and procedures to various departments. S

Exciting new contract with our key Biotech client in the Bay Area for an initial 6 month contract, with extension likely. Ideal candidate will be experienced with Veeva Systems and have previous experience in training the GxP Quality Systems... The Opportunity: Manage and maintain the GxP document control system, which includes product-related documentation, quality manuals, external documents, departmental procedures, and work instructions. Coordinate all aspects of incoming, in-process, and completed document change controls, ensuring supporting documentation is provided, changes are completed, and documentation is properly closed out and released. Oversee and maintain the GxP training program, including assigning training, archiving completed records, monitoring compliance, and conducting periodic audits of training records. Train new users on the document control and training systems, as needed. Provide guidance on document control practices and procedures to various departments. S

Exciting new contract with our key Biotech client in the Bay Area for an initial 6 month contract, with extension likely. Ideal candidate will be experienced with Veeva Systems and have previous experience in training the GxP Quality Systems... The Opportunity: Manage and maintain the GxP document control system, which includes product-related documentation, quality manuals, external documents, departmental procedures, and work instructions. Coordinate all aspects of incoming, in-process, and completed document change controls, ensuring supporting documentation is provided, changes are completed, and documentation is properly closed out and released. Oversee and maintain the GxP training program, including assigning training, archiving completed records, monitoring compliance, and conducting periodic audits of training records. Train new users on the document control and training systems, as needed. Provide guidance on document control practices and procedures to various departments. S

Exciting new contract with our key Biotech client in the Bay Area for an initial 6 month contract, with extension likely. Ideal candidate will be experienced with Veeva Systems and have previous experience in training the GxP Quality Systems... The Opportunity: Manage and maintain the GxP document control system, which includes product-related documentation, quality manuals, external documents, departmental procedures, and work instructions. Coordinate all aspects of incoming, in-process, and completed document change controls, ensuring supporting documentation is provided, changes are completed, and documentation is properly closed out and released. Oversee and maintain the GxP training program, including assigning training, archiving completed records, monitoring compliance, and conducting periodic audits of training records. Train new users on the document control and training systems, as needed. Provide guidance on document control practices and procedures to various departments. S

Exciting new contract with our key Biotech client in the Bay Area for an initial 6 month contract, with extension likely. Ideal candidate will be experienced with Veeva Systems and have previous experience in training the GxP Quality Systems... The Opportunity: Manage and maintain the GxP document control system, which includes product-related documentation, quality manuals, external documents, departmental procedures, and work instructions. Coordinate all aspects of incoming, in-process, and completed document change controls, ensuring supporting documentation is provided, changes are completed, and documentation is properly closed out and released. Oversee and maintain the GxP training program, including assigning training, archiving completed records, monitoring compliance, and conducting periodic audits of training records. Train new users on the document control and training systems, as needed. Provide guidance on document control practices and procedures to various departments. S

Major Responsibilities: Responsible for all aspects of assigned Program as Quality Engineer, including internal quality performance objectives, customer interface, program IPT (integrated product team), and program supplier quality support. Major Responsibilities: Schedules and maintains milestones and timeline tracking for key objectives. Performs Preliminary Reviews of DMRs and evaluates in-process rejections via QA Process procedures for Non-conforming Material and MRB Activity. Performs drawing control and CCB review activities for new and revised documents, ensuring customer notification of all changes. Performs Product Sell-Off included final work order test data package review prior to shipment to ensure product performance is within specified standards. Ensures Programs supplier quality issue resolution through coordination of resources and support of QC, Purchasing and Engineering groups. Interface with various company departments to assist in resolve quality problems and prov