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Quality Assurance Document Control Associate Jobs in Michigan

... infection control, and competency programs Coordinate OHC's quarterly clinical record review ... documentation is complete, accurate, and reflects delivery and legal requirements Monitors ...

... to Quality Assurance Associates and is responsible for ensuring organizational adherence to ... documentation, corrective actions, and regulatory compliance. * Supervise Quality Assurance ...

The company's portfolio now includes automation control, motion control, vibration control and ... Document discrepancies detected during inspection and communicate findings, both verbally and in ...

... maintain documentation • Support customers both remotely and in person • Assist with ... Associate or bachelor's degree in a technical discipline • Experience with aviation refueling ...

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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 Managing version control requires meticulous attention to detail to prevent outdated documents from being used in production or audits.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 Michigan? The most popular types of Quality Assurance Document Control jobs in Michigan are:
What cities in Michigan are hiring for Quality Assurance Document Control Associate jobs? Cities in Michigan with the most Quality Assurance Document Control Associate job openings:

Quality Assurance Assistant

Weldaloy Specialty Forgings

Warren, MI • On-site

$20 - $22/hr

Full-time

Re-posted 20 days ago


Job description

Position Title: Quality Assurance Assistant

Reports To: Quality Engineer & Supervisor

Supervises: None

Classification: Hourly, non-exempt, non-union

Position Summary

The Quality Assurance Assistant (QA Assistant) is responsible for executing documentation preparation and customer approval workflows to support manufacturing and quality operations. This role ensures that required documentation, certification packages, and customer submittals are completed accurately, on time, and in compliance with internal procedures and customer requirements. The QA Assistant plays a critical transactional role within the Quality organization by managing document preparation (WC 970) and customer approval workflows (WC 971), enabling Quality Engineers to focus on technical decision-making, corrective actions, and quality system governance. The position works closely with Quality Technicians, Quality Engineers, Metallurgy, and Engineering to gather required information and ensure complete and accurate documentation.

Essential Duties & Responsibilities:

The statements below are intended to describe the general nature and level of work being performed by the employee of this position. They are not intended to be an exhaustive list of all responsibilities and activities required of this position.

  • Prepare quality documentation packages to support production and customer requirements
  • Compile and organize required documentation, including: Certifications, inspection reports, material documentation, and supporting technical records
  • Ensure documentation is complete, accurate, and formatted per internal and customer standards
  • Verify that all required documentation components are included prior to submission
  • Submit documentation packages to customers for approval
  • Track approval status and follow up as needed to ensure timely completion
  • Maintain records of submissions, approvals, and revisions
  • Coordinate responses to customer documentation-related requests
  • Ensure all required inputs are obtained to complete document packages
  • Escalate missing or unclear information to appropriate stakeholders
  • Maintain organized records of documentation and approvals
  • Enter and update documentation status within ERP/QMS systems (e.g., Plex)
  • Ensure traceability and accessibility of documentation
  • Follow established procedures, templates, and workflows
  • Identify inefficiencies or recurring issues in documentation processes
  • Support continuous improvement efforts related to: document cycle time, first-pass quality, and workflow consistency
  • Additional duties as assigned.

Requirements:

To perform this position successfully, the employee must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.

This position involves access to technical data that is subject to the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR), which define a U.S. person to include a U.S. citizen, lawful permanent resident (green card holder), or a protected individual as defined by 8 U.S.C. 1324b(a)(3). Employment is contingent upon the applicant's ability to meet these requirements or the Company's ability to obtain an export license on the applicant's behalf.

  • Minimum of a high school diploma or GED equivalent and at least two years of related experience and/or equivalent education & experience
  • Knowledgeable in ISO 9001 Quality Standards, AS9100 preferred.
  • Previous working experience with document control
  • Demonstrated knowledge of document preparation is required, AS9102 is highly desired.
  • Previous experience using an ERP system is desired, preferably PLEX.
  • Proficient in Microsoft Excel, Word, Outlook.
  • Demonstrated problem solving skills and excellent organizational and communication skills.
  • Ability to multi-task.
  • Position is required to be on-site, occasional work from home with supervisor approval is available.
  • Supports and demonstrates the Company's core values.

Working Conditions:

This position is designed to work full-time. Days and hours of work are typically Monday through Friday, 8:00 a.m. to 5:00 p.m. An alternate schedule may be arranged or assigned based on the business demands, nature of duties performed, and other factors. Occasional flexibility to work evenings or weekends may be required as job responsibilities demand. Regular work, after hours and/or weekend work may be performed remotely, if the capability exists. This position mainly operates in an office environment during work hours, but may be expanded to assist and support employees in other departments within the Company; Occasional exposure to production equipment and machinery. The employee will manage multiple priorities daily and may be interrupted frequently to meet the needs and requests of employees. The environment may be busy and noisy. All required personal protective equipment is provided.

Physical Demands:

While performing the duties of this job, the employee will spend most of his/her time sitting using computers and standard office equipment such as phones, photocopiers and fax machines. Occasional moving and/or lifting of 10 pounds, stooping, bending and reaching with hands and arms. While performing these job duties, the employee is regularly required to see, talk, and hear.

Weldaloy Products Company provides Equal Employment Opportunity (EEO) to all applicants without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, genetic information, marital status, veteran status, height, weight or arrest record in accordance with applicable federal, state and local laws.