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Quality Assurance Document Control Associate Jobs in Missouri

... documentation; managing staff. Involved in the process to plan, coordinate, organize and control of ... Associate's degree from an accredited college or university in a technical, engineering, or quality ...

... documentation; managing staff. Involved in the process to plan, coordinate, organize and control of ... Associate's degree from an accredited college or university in a technical, engineering, or quality ...

... documentation; managing staff. Involved in the process to plan, coordinate, organize and control of ... Associate's degree from an accredited college or university in a technical, engineering, or quality ...

QA/QC Coordinator

Kansas City, MO · On-site

$19.25 - $26.50/hr

Join Our Team as a QA/QC Coordinator at E2 Optics! Are you ready to elevate your career with an award-winning, Woman-Owned technology integrator that's leading the charge in the data center ...

Review and improve test coverage, regression testing processes, QA documentation, and overall quality assurance methodologies. * Contribute to the continuous improvement of QA tools, workflows, and ...

Be Seen First

Position Summary The Quality Assurance Technician plays a crucial role in ensuring that products ... equipment or quality control instruments is a plus. * Experience in data documentation and ...

... or quality control instruments is a plus. o Experience in data documentation and reporting (using Microsoft Office or specialized software) is important. Key Skills: • Attention to Detail:

Showing results 21-40

Quality Assurance Document Control Associate information

What is a quality assurance document control associate?

A Quality Assurance Document Control Associate is responsible for managing, organizing, and maintaining documentation related to quality assurance processes within an organization. They ensure that all quality documents, such as standard operating procedures (SOPs), work instructions, and records, are accurate, up-to-date, and comply with regulatory requirements. Their role often involves reviewing, issuing, archiving, and tracking documents, as well as supporting audits and ensuring that employees use the correct versions of documents. This position is critical in industries like pharmaceuticals, biotechnology, and manufacturing, where document control is vital for regulatory compliance and quality management.

What are the main challenges quality assurance document control associates face when managing document version control in regulated industries?

Quality Assurance Document Control Associates often encounter challenges ensuring all documents are current, accurate, and accessible to authorized personnel, especially in highly regulated industries like pharmaceuticals or medical devices. Managing version control requires meticulous attention to detail to prevent outdated documents from being used in production or audits. Additionally, coordinating timely reviews and approvals from multiple stakeholders can be complex, making strong organizational and communication skills essential for success in this role.

What are the key skills and qualifications needed to thrive as a quality assurance document control associate?

To thrive as a Quality Assurance Document Control Associate, you need strong organizational skills, attention to detail, and familiarity with regulatory requirements, often supported by a degree in life sciences or a related field. Proficiency with document management systems (DMS), electronic quality management systems (eQMS), and standards such as ISO or FDA regulations is crucial. Effective communication, time management, and the ability to work meticulously under deadlines are valuable soft skills for this role. These competencies ensure the accuracy, compliance, and efficient handling of critical documentation, which is essential for maintaining quality standards in regulated industries.

What is the difference between Quality Assurance Document Control Associate vs Quality Assurance Specialist?

AspectQuality Assurance Document Control AssociateQuality Assurance Specialist
Primary RoleManage and maintain quality documentation, ensure document accuracy, control revisionsDevelop, implement, and monitor quality assurance processes and procedures
Required CredentialsTypically a high school diploma or associate degree; familiarity with document management systemsBachelor's degree in quality, engineering, or related field; certifications like CQE often preferred
Work EnvironmentOffice setting, regulated industries like pharmaceuticals, manufacturingLaboratory, manufacturing, or quality assurance departments in similar industries
Key FocusDocument control, compliance, record keepingProcess improvement, quality audits, compliance management

While both roles support quality assurance, the Document Control Associate primarily handles documentation and record management, whereas the Quality Assurance Specialist focuses on developing and overseeing quality processes. The Associate role is more administrative, while the Specialist role involves active process improvement and compliance oversight.

What are the most commonly searched types of Quality Assurance Document Control jobs in Missouri? The most popular types of Quality Assurance Document Control jobs in Missouri are:

Entry Level - Document Control Specialist

Eurofins Scientific

Columbia, MO • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Eurofins rating

7.4

Company rating: 7.4 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

69th of 120 rated laboratories


Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

*This is an entry level opportunity:

  • Maintain document control records and accurately enter new procedures, and print associated reports as needed. Make sure all files are accurate and precise, so that one can be 100% positive what is indicated at all times is accurate
  • Maintain accurate posting of procedures on internal system; archive revised procedures in a timely manner
  • Perform word processing of procedures as required and understand and recognize QA requirements for procedure formatting
  • Back up Archives
  • Back up other departmental duties as needed
  • Conducts all activities in a safe and efficient manner
  • Performs other duties as assigned
Qualifications

Minimum Qualifications:

  • High school diploma or equivalent
  • Excellent attendance
  • Able to work quickly and accurately in a fast paced environment
  • Clerical experience is desired
  • Knowledge of basic office equipment (faxes, copiers, printers, etc.)
Additional Information

Position is full-time, Monday-Friday 8am-5pm. Candidates within a commutable distance of Columbia, MO are encouraged to apply.

Excellent full-time benefits including:

  • Comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.


What Eurofins employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US