Document Qa - 53+ job offers

*Key Responsibilities:** Manage and maintain paper-based controlled documentation systems (no electronic document management system), ensuring proper filing, storage, and accessibility of all quality records Own the full lifecycle of controlled documents, including creation, revision, approval, issu

QA Document Control Specialist 📍 Location: On-site (Connecticut) 🕒 Schedule: Full-Time 💰 Salary Range: $72,000 - $90,000/year (based on experience) Position Overview The QA Document Control Specialist will play a key role in maintaining quality documentation, supporting compliance efforts, and as

QA Document Control Specialist 📍 Location: On-site (Connecticut) 🕒 Schedule: Full-Time 💰 Salary Range: $72,000 - $90,000/year (based on experience) Position Overview The QA Document Control Specialist will play a key role in maintaining quality documentation, supporting compliance efforts, and as

*QA Document Control Associate (3-Month Contract) | GMP | On-site** I’m currently working with a *biologics-focused CDMO** who are continuing to expand their Quality function as they scale GMP operations across the US. As part of this growth, they are looking to bring on a *QA Document Control Contr

*Job Title:** QA Associate - Document Management *Shift:** Monday to Friday, Days. *About Us: this is who we are** At **Just** **E****votec Biologics**, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, lea

*Nature and Scope** To perform, maintain and update logs and databases. Create and maintain controlled templates. Support document formatting. *Essential Duties And Responsibilities** Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to th

Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics’ mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics’ lead product candidate is a

Job Title: Documentation Specialist Location : Bedford, Ohio Job Type : Full-time Job ID: 10792 About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ purpose is to put better health within reach, every day for millions of pati

The *QA Associate I *will provide support for the QA Systems team including Veeva DMS, Retention and Verification.<br /><br />* 1st shift ~8a-5p M-F<br />* Pay: $25-30/hr<br />* Starts out on a contract (position is open due to current contracting converting on full time!)&lt

A leading industrial company located in Henderson, Texas, is looking for a qualified candidate to manage administrative tasks in document control. The role involves high-volume document tracking, record accuracy checks, and collaboration with teams in the oil and gas industry. Candidates should have

A leading health and wellness company in Pleasant Grove, UT is seeking a Quality Assurance Document Control Specialist II. You will be responsible for managing documentation services, including technical writing and compliance with GMP practices. Candidates should have 2 - 4 years of document contro

Quality Assurance Document Control (QADC) Associate Specialist Location: Bothell, WA Onsite Shift: Friday-Monday 2pm-10:30pm Top Skills: Strong communication and customer service skills. Innovation Able to prioritize, manage time well, multi-task, and troubleshoot effectively Smartsheet and Excel ex

Quality Assurance Document Management This is a 100% onsite position. Assists in maintaining a compliant, efficient Quality Assurance Document Management program. Under direct supervision, perform day-to-day Document Control activities: process DCR packages and review for correctness and completenes

Job Title: QA Associate - Document Management Shift: Monday to Friday, Days. About Us: this is who we are At Just E votec Biologics , we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each oth

RRD is a leading global provider of marketing, packaging, print, and supply chain solutions that elevate engagement across the complete customer journey. The company offers the industry’s most trusted portfolio of creative execution and world-wide business process consulting, with services designed

Company Description RRD is a leading global provider of marketing, packaging, print, and supply chain solutions that elevate engagement across the complete customer journey. The company offers the industry’s most trusted portfolio of creative execution and world-wide business process consulting, wit

*Company Description** RRD is a leading global provider of marketing, packaging, print, and supply chain solutions that elevate engagement across the complete customer journey. The company offers the industry’s most trusted portfolio of creative execution and world-wide business process consulting,

RRD is a leading global provider of marketing, packaging, print, and supply chain solutions that elevate engagement across the complete customer journey. The company offers the industry’s most trusted portfolio of creative execution and world-wide business process consulting, with services designed

Controlled Document Lifecycle And Records Management Specialist Nature And Scope To perform, maintain and update logs and databases. Create and maintain controlled templates. Support document formatting. Essential Duties And Responsibilities Nothing in this job description restricts management's rig

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular dise