CrawlJobs Logo

Quality Document Control Specialist

United States, Tempe 28.00 - 35.00 USD / Hour · Job Posted January 11, 2026
Apply Position
Job Link Share

Job Description

This position is responsible for the creation and processing of all change request packets, creation of controlled documents, tracking of packets and all associated paperwork involved. This requires participation as an active team member in cross functional teams and ownership of project team documentation. Responsibilities also include the origination, editing and revision of technical documentation. This position will also assist with the migration between two different MasterControl systems.

Job Responsibility

  • Creation and processing of all change request packets
  • Creation of controlled documents
  • Tracking of packets and all associated paperwork
  • Participation as an active team member in cross functional teams and ownership of project team documentation
  • Origination, editing and revision of technical documentation
  • Assist with the migration between two different MasterControl systems
  • Participates in regulatory compliance audits and inspections
  • Participates in investigations
  • Completes applicable job-specific training
  • Effectively manage the end-to-end change lifecycle and identify process improvements where possible
  • Day to day management of change requests
  • Reporting of change to both internal and customer management teams
  • Identify and drive continuous improvements to the quality and efficiency of the change management process
  • Applies skills and develops documentation including operating procedures, process flow charts and manufacturing procedures
  • Documentation origination, editing and revision
  • Creation of change request and associated paperwork utilizing the Electronic Document Management System (EDMS)
  • Uses various computer software applications to complete assigned work activities
  • Understanding of compliance requirements and regulations Ability to generate report(s) utilizing the systems
  • Work with teams to determine status of projects/document changes and assist with driving project/document changes to completions
  • Be able to develop and speak to metrics and workload tracking
  • Be actively engaged in meetings
  • Participates in the development of solutions to Quality System problems and/or non-compliance
  • Assists in maintenance of department, site / business unit, and corporate procedures and policies
  • Demonstrates knowledge of operating procedures and expertise in a specific functional area
  • Accountable for the execution of specific tasks with moderate discretion and with oversight from a supervisor
  • Carries out tasks and activities
  • Applies specialized knowledge/skills to perform routine and non-routine work of a group or department
  • Other duties, as assigned

Requirements

  • Quality Management Systems experience
  • Document Controls experience
  • Medical device industry experience
  • Highschool diploma and at least 1+ year experience in documentation related position
  • Basic understanding of regulations
  • Advanced language proficiency in reading, writing, understanding, and communicating in English
  • Attention to detail
  • Intermediate computer skills and software applications, including experience with Microsoft Office tools (Outlook, Word, Excel, PowerPoint)
  • Intermediate organizational and administrative skills
  • Experience in working in a cross-functional team environment as well as the ability to function independently
  • Ability to gather and organize information
  • Ability to grasp technical terms, processes, and methods
  • Ability to handle a variety of projects at the same time
  • Ability to prioritize and organize a busy and changing workload
  • Ability to work in a team environment and/or independently with little supervision
  • Works collaboratively with a variety of people at all levels within the organization to ensure effective communication and success of key initiatives
  • Resolve problems by clarifying issues
  • researching and exploring answers and alternative solutions
  • implements solutions
  • escalates unresolved problems
  • Ability to be flexible in work schedule, including a willingness to work overtime as needed
  • Positive and Professional attitude

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Quality Document Control Specialist

8 matching positions

New

Quality Control Specialist, Microbiology

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...
Location
Location
United States , Thousand Oaks
Salary
Salary:
100450.45 - 135903.55 USD / Year
amgen.com Logo
Amgen
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • High school diploma / GED and 10 years of Quality, Microbiology or Operations experience OR Associate’s degree and 8 years of Quality, Microbiology or Operations experience OR Bachelor’s degree and 4 years of Quality, Microbiology or Operations experience OR Master’s degree and 2 years of Quality, Microbiology or Operations experience OR Doctorate degree
Job Responsibility
Job Responsibility
  • Lead microbial identification activities, organism assessments, and support routine and non-routine microbiological testing
  • Provide leadership for microbiology laboratory operations, coordinate daily priorities, supervise laboratory staff, and support weekend laboratory operations
  • Own and lead complex microbiological investigations, deviations, environmental monitoring excursions, and contamination events, including root cause analysis, risk assessments, and product impact assessments
  • Provide technical expertise for environmental monitoring, bioburden control, microbial identification, contamination control strategies, and laboratory controls
  • Author and drive CAPAs, microbial risk assessments, and change controls to ensure compliant resolution of quality events
  • Coordinate contract laboratory activities, including testing support, data review, investigation collaboration, and approval of associated documentation
  • Generate and maintain complete, accurate, and inspection-ready documentation using electronic laboratory and quality systems (e.g., LMES, LIMS, CIMS, and Veeva)
  • Partner with Quality, Manufacturing, Engineering, and global microbiology teams to support process improvements, operational excellence initiatives, regulatory inspections, and strategic microbiology projects
What we offer
What we offer
  • A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
  • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
  • Stock-based long-term incentives
  • Award-winning time-off plans
  • Flexible work models where possible
  • Fulltime
Read More
Arrow Right

Quality Control Specialist - 2nd Shift

Test and monitors products for compliance per specifications.
Location
Location
United States , Carthage
Salary
Salary:
Not provided
ajinomotofoods.com Logo
Ajinomoto Foods North America, Inc.
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Prefer High School Diploma/GED
  • Be able to work in a fast-paced environment
  • Strong attention to detail and the ability to work rapidly and with a high degree of accuracy
  • Math Skills
  • Reliable, Self-Driven, Minimum Supervision
  • Must be able to read and write English
Job Responsibility
Job Responsibility
  • Evaluates products for compliance per specifications
  • Understanding, evaluating and executing the tests, and procedures properly
  • Maintaining and setting up documentation and control procedures
  • Picking up samples and carrying out checks and tests
  • Understanding and comprehending Product Vision guidelines for quality aspects
  • Follow all safety rules and regulations per established company policies
  • Perform all other duties as assigned
  • Follows established equipment Lockout/Tagout procedures as required
  • Fulltime
Read More
Arrow Right

Document Control Specialist

The successful candidate will serve as a Document Control Specialist within the ...
Location
Location
United States , Moffett Field
Salary
Salary:
55000.00 - 115000.00 USD / Year
amentum.com Logo
Amentum
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • A certificate, associate's degree, bachelor's degree, or relevant experience in a related field is desired. Verified coursework or experience in a related field may also be considered.
  • Strong organizational skills, high attention to detail, and desire to learn new skills.
  • Experience with document control processes or configuration management preferred.
  • Proficient with Microsoft Office applications, SharePoint, Confluence, or similar content management tools.
  • Ability to work collaboratively with technical staff and SMEs.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple tasks and deadlines in a fast‑paced environment.
  • This position also requires the candidate to complete on-the-job safety training to perform assigned work activities.
  • Must be able to obtain a NASA badge and gain access to the facilities.
Job Responsibility
Job Responsibility
  • Manage the full lifecycle of documents, including creation, revision, approval, publication, archiving, and periodic review.
  • Review incoming Document Change Requests for accuracy, completeness, and compliance with established guidelines.
  • Coordinate with subject matter experts and document owners to gather required updates and ensure technical accuracy.
  • Update and maintain internal and external web pages per stakeholder requests.
  • Upload new or revised documents, confirm accessibility, and verify that restricted documents remain protected.
  • Coordinate with engineering, quality, configuration management, and operations staff to ensure documentation aligns with current workflows and system updates.
  • Assist with general administrative activities within the Wind Tunnel Division as assigned.
What we offer
What we offer
  • Health, dental, and vision insurance
  • Paid time off and holidays
  • Retirement benefits (including 401(k) matching)
  • Educational reimbursement
  • Parental leave
  • Employee stock purchase plan
  • Tax-saving options
  • Disability and life insurance
  • Pet insurance
  • Fulltime
Read More
Arrow Right

Document Control Specialist

JR Automation, a Hitachi Group Company, is driven to deliver customer success wo...
Location
Location
United States , Holland
Salary
Salary:
Not provided
jrautomation.com Logo
JR Automation
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's Degree preferred, Associate's Degree required
  • 1-3 years of working experience in Document Control or related role building and maintaining QMS
  • Experience auditing to ISO 9001:2015 or similar standard
  • Can write accurate technical documents with clarity, concision, and consistency
  • Can produce documents that serve the needs of appropriate audiences, as well as edit documents created by others to ensure overall quality and professionalism
  • Can confidently communicate and collaborate through a variety of mediums with a variety of employees, ranging in function and personality
  • Can collect feedback from varying stakeholders and integrate and/or moderate ideas to produce quality documents and document management
  • Possesses the ability to identify and rectify inconsistencies, gaps, or other areas for improvement in all internal documents
  • Attention to detail must be executed regarding content, formatting, grammatical accuracy, and document deliverables
  • Ability to stay on task while ensuring a variety of activities can be completed within deadlines
Job Responsibility
Job Responsibility
  • Serve as the QMS documentation subject-matter expert (SME), providing guidance on documentation requirements, adequacy, and compliance status
  • Lead cross-functional teams of process owners, content experts, and functional SMEs through document harmonization efforts, including coordination of multiple change requests
  • Communicate document changes and administer employee notifications
  • Evaluate business processes to ensure compliance with quality requirements and evolving business needs
  • facilitate or participate in continuous improvement initiatives
  • Manage master project folder templates and support teams during project folder compliance audits
  • Assist with administration and ongoing maintenance of the organizational Knowledge Base database
  • Support the Quality Manager in maintaining site compliance with ISO 9001:2015 requirements
  • Train management and employees on ISO 9001:2015 standards and QMS expectations
  • Support Quality and Regulatory plans, implementation, and capability-building efforts as the business grows
What we offer
What we offer
  • Competitive wages
  • medical benefits starting your first day
  • paid parental leave
  • Opportunity to work on customized, 1-of-1 automation projects
  • A collaborative, engineering-driven environment
  • Career growth and skill development opportunities
  • A role where craftsmanship and quality truly matter
  • Work with cutting edge and innovative technologies
  • Fulltime
Read More
Arrow Right

Quality Control Specialist

We are looking for a detail-oriented Quality Control Specialist to support inspe...
Location
Location
United States , Washougal
Salary
Salary:
Not provided
https://www.roberthalf.com Logo
Robert Half
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Hands-on experience performing quality control inspections in a manufacturing or production setting.
  • Ability to use common measurement and inspection tools with accuracy and consistency.
  • Working knowledge of blueprint reading, technical drawings, and basic GD&T interpretation.
  • Experience creating or supporting AS9102 First Article Inspection reports.
  • Proficiency in Microsoft Word and Excel for reporting, tracking, and documentation.
  • Familiarity with quality management systems such as AS9100 and ISO 9001.
  • Strong attention to detail with the ability to identify discrepancies and document findings clearly.
Job Responsibility
Job Responsibility
  • Conduct visual and dimensional inspections of parts and assemblies using precision instruments such as micrometers, calipers, dial indicators, comparators, and related gauges.
  • Gather, track, and communicate quality results, including nonconforming trends and in-process rejection data, to support production and quality teams.
  • Review engineering drawings and 3D models to verify product compliance, applying a working knowledge of GD&T during inspection activities.
  • Prepare AS9102 First Article Inspection documentation with accuracy and completeness for customer and internal quality requirements.
  • Support root cause reviews and corrective action follow-up by assisting with troubleshooting efforts and monitoring outstanding quality items.
  • Maintain inspection records and reports in Microsoft Word and Excel to ensure documentation is organized, clear, and audit ready.
  • Follow established safety procedures at all times and demonstrate sound judgment while handling parts, tools, and inspection equipment.
  • Work within structured quality management standards, including AS9100 and ISO 9001 environments, to help sustain compliance and process consistency.
What we offer
What we offer
  • medical
  • vision
  • dental
  • life and disability insurance
  • 401(k) plan
Read More
Arrow Right

Quality Control Specialist

Every day, we get opportunities to make a positive impact – on our colleagues, p...
Location
Location
United States , Broken Arrow
Salary
Salary:
88000.00 - 104000.00 USD / Year
alfalaval.it Logo
ALFA LAVAL ITALY S.R.L.
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree, associate’s degree, or relevant experience in quality management or a related field
  • 8 years of experience in quality assurance, quality control, and/or inspection within a regulated manufacturing industry
  • Conducted thorough root-cause analysis and ensured 100% completion of non-conformance dispositions in accordance with company guidelines
  • Maintained comprehensive documentation of material scrap and rework analysis for all relevant cases
  • Successfully completed and documented continuous improvement activities and projects, ensuring all records are on file
  • Working knowledge of the ASME section II, V, VIII and IX and related standards preferred
  • Familiarity with ISO9000:2000 standard, material specifications, and various national/international codes and standards
  • Must be able to demonstrate knowledge of welding inspections
  • Welding inspections experience at manufacturer shops / facilities
  • Understanding of jurisdictional pressure vessel laws and Quality Assurance principles and systems
Job Responsibility
Job Responsibility
  • Review project specifications to define and apply customer quality requirements
  • Document inspection and testing activities according to established procedures
  • Support development and qualification of weld procedures
  • Collaborate with manufacturing teams to implement project quality standards
  • Coordinate with third-party inspectors and manage inspection documentation
  • Lead in inspections and Customer audits
  • Recommend and implement improvements to the quality management system
  • Oversee document control processes within the Quality Department
  • Conduct audits and evaluations across production, engineering, and quality functions
  • Support corrective and preventive actions for nonconforming materials and products
What we offer
What we offer
  • medical/dental/vision/life
  • 401(k) plan
  • competitive salary and full benefits package
  • Fulltime
Read More
Arrow Right

Specialist, Quality Control, Chemistry

As a QC Specialist – Chemistry, you will play a key role in ensuring the quality...
Location
Location
Spain , Madrid
Salary
Salary:
Not provided
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • BA/BS in Chemistry (preferred) or other relevant scientific discipline with 2-5 years' experience. A student in an undergraduate program (BA/BS) is acceptable.
  • 2-5 years of experience in quality control laboratory of a pharmaceutical company
  • Hands on experience with analytical chemistry testing including chromatographic techniques- HPLC, UPLC, Spectroscopic and Spectrometric techniques
  • Physical properties techniques such as Particle Analysis by Dynamic Light Scattering and others.
  • Working experience in a GMP environment.
  • Working knowledge of relevant and current FDA, EU, ICH guidelines and regulations preferred.
  • Ability to collaborate effectively in a dynamic, cross-functional matrix environment.
  • Ability to efficiently prioritize and complete multiple projects and tasks in a fast-paced environment.
  • This position is site-based, requiring you to be at Moderna's site full-time.
  • Proficiency in English (verbal and/or written) required due to global collaboration needs.
Job Responsibility
Job Responsibility
  • Performing routine analytical chemistry testing such as HPLC, UPLC, UV, particle analysis, and dynamic light scattering.
  • Executing and supporting stability studies and GMP release testing.
  • Managing LIMS (LabVantage) sample result entries and executing electronic assay forms.
  • Assisting with method transfers and development activities across the QC Chemistry function.
  • Supporting special projects and ongoing initiatives in QC laboratory optimization and compliance.
  • Performing general laboratory operations including sample management, reagent preparation, equipment maintenance, and lab housekeeping.
  • Completing and maintaining cGMP documentation and ensuring full data integrity compliance.
  • Writing and revising SOPs, protocols, and reports in accordance with internal and external requirements.
  • Contributing to the training and troubleshooting activities for more junior staff.
  • Participating in investigations, deviations, change controls, and CAPAs within quality systems.
What we offer
What we offer
  • Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being with access to fitness, mindfulness, and mental health support
  • Family building benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras
  • Fulltime
Read More
Arrow Right

Mechanical and Plumbing Quality Control Specialist

The Mechanical and Plumbing Quality Control (QC) Specialist will conduct indepen...
Location
Location
United States , St Petersburg
Salary
Salary:
Not provided
powerdesigninc.us Logo
Power Design
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Solid knowledge of the multi-family mechanical and plumbing industry and relevant codes, including IMC, IPC, NCCER and ASHRAE standards
  • Experience with Hydronic piping systems, Chiller, Boiler, Water Source Heat Pump, and Refrigeration systems
  • 8-10 years mechanical and plumbing experience
  • Journeyman plumber’s or HVAC technician’s license required
  • master’s license preferred
  • Must be detail-oriented and quality-driven
  • Able to travel up to 50% of the time
  • Strong written, verbal, and interpersonal communication skills required
  • Proficient in Microsoft Office, including Excel, Word, and Outlook
  • Ability to interact with employees at all levels, from field personnel to executive management
Job Responsibility
Job Responsibility
  • Prepare for evaluation by gathering and reviewing contract documents, reports, and coordination drawings, as well as meeting with key personnel to discuss project specifics
  • Follow work program steps for each mechanical and plumbing scope to determine if job conditions meet expectations
  • Identify and document any items observed needing improvement/attention in addition to specific work program items
  • Provide training on installation methods and/or best practices to project teams when needed
  • Represent the Quality Assurance department positively through interaction with Project Superintendent and Foreman
  • Deliver accurate and concise evaluation reports and photo documentation
  • Communicate with customers prior to evaluation, while on-site, and following evaluation to discuss progress, satisfaction, and needs
  • Meet with executive management and project teams to communicate evaluation results and recommend action plans for improvement
  • Render impartial and unbiased judgment by remaining independent and objective
  • Maintain accurate, organized records
Read More
Arrow Right