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Part Time Iso Document Control Jobs (NOW HIRING)

Address 3350 Monte Villa Parkway Type Employee Full Time/Part Time Full Time Overview As one of the ... Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness

Quality Control Technician

Strongsville, OH · On-site

$17.25 - $22.25/hr

Perform testing and document results in accordance with the Company's procedures, drawings, test ... Ability to write up non-conforming product per established ISO procedures. * Prep and review ASME ...

Quality Control Technician

Strongsville, OH · On-site

$17.25 - $22.25/hr

Perform testing and document results in accordance with the Company's procedures, drawings, test ... Ability to write up non-conforming product per established ISO procedures. * Prep and review ASME ...

Telework Type: Part-Time Telework * Work Location: Houston, TX Extraordinary teams building ... Ensure version control and document integrity for training materials. * Coordinate implementation ...

Telework Type: Part-Time Telework * Work Location: Houston, TX Extraordinary teams building ... Ensure version control and document integrity for training materials. * Coordinate implementation ...

$17.75 - $22.50/hr

Perform testing and document results in accordance with the Company's procedures, drawings, test ... Ability to write up non-conforming product per established ISO procedures. * Prep and review ASME ...

$17.50 - $22.25/hr

Perform testing and document results in accordance with the Company's procedures, drawings, test ... Ability to write up non-conforming product per established ISO procedures. * Prep and review ASME ...

Perform document control activities including scanning, file conversion, formatting, PDF assembly ... * Part-time, non-exempt hourly position * Paid sick leave in accordance with California law

Perform document control activities including scanning, file conversion, formatting, PDF assembly ... * Part-time, non-exempt hourly position * Paid sick leave in accordance with California law

$17.50 - $22.25/hr

Perform testing and document results in accordance with the Company's procedures, drawings, test ... Ability to write up non-conforming product per established ISO procedures. * Prep and review ASME ...

Showing results 41-60

Part Time Iso Document Control information

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$10

$21

$31

How much do part time iso document control jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for part time iso document control in the United States is $21.73, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.00 per hour, depending on experience, location, and employer.

What is a part time ISO document control?

A Part Time ISO Document Control job involves managing, organizing, and maintaining documents related to ISO standards and quality management systems for an organization. This role typically includes tasks such as updating, distributing, and archiving controlled documents, ensuring compliance with company and regulatory requirements, and supporting audits. Working part-time means the role has reduced hours compared to a full-time position, making it suitable for individuals seeking flexible work arrangements. Strong attention to detail and familiarity with document management systems are important for this job.

What are the key skills and qualifications needed to thrive as a part time ISO document control?

To thrive as a Part Time ISO Document Control, you need strong organizational skills, attention to detail, and a good understanding of ISO standards, typically supported by experience in document management or quality assurance. Familiarity with document control software, electronic document management systems (EDMS), and sometimes ISO 9001 certification is often required. Excellent communication, time management, and the ability to work independently are valuable soft skills for this role. These skills ensure accurate documentation, compliance with quality standards, and efficient workflow in regulated environments.

What are some common challenges faced by part time ISO document control professionals, and how can they be effectively managed?

Part-time ISO Document Control professionals often face the challenge of staying updated with frequent document revisions and ensuring timely communication across departments, despite limited work hours. Balancing workload and maintaining document accuracy requires strong organizational skills and efficient time management. Proactively setting clear priorities, utilizing document management systems, and maintaining open communication with team members can help manage these challenges and ensure compliance with ISO standards.

What is the difference between Part Time Iso Document Control vs Part Time Quality Assurance Coordinator?

AspectPart Time Iso Document ControlPart Time Quality Assurance Coordinator
CredentialsISO standards knowledge, basic administrative skillsQuality assurance certifications, administrative skills
Work EnvironmentOffice setting, document management systemsOffice or plant environment, quality processes
Industry UsageManufacturing, engineering, or compliance sectorsManufacturing, healthcare, or service industries
Common Search IntentManaging ISO documentation, compliance tasksMonitoring quality processes, audits

Part Time Iso Document Control focuses on managing ISO-related documents and ensuring compliance with standards, while Part Time Quality Assurance Coordinator oversees quality processes and audits. Both roles require administrative skills but differ in their specific focus areas within the industry.

More about Part Time Iso Document Control jobs

What cities are hiring for Part Time Iso Document Control jobs?

Cities with the most Part Time Iso Document Control job openings:

What are the most commonly searched types of Iso Document Control jobs?

The most popular types of Iso Document Control jobs are:

What are popular job titles related to Part Time Iso Document Control jobs?

For Part Time Iso Document Control jobs, the most frequently searched job titles are:

Infographic showing various Part Time Iso Document Control job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 73% Full Time, 22% Part Time, 3% Contract, and 1% Nights. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $45,201 per year, or $21.7 per hour.

Title QC Inspector

Bothell, WA • On-site

Bruker
Biotechnology Research and Development • 5 - 10K employees

$41K/yr

Full-time, Part-time

Medical, Dental, Life, Retirement, PTO

Re-posted yesterday


Bruker rating

7.4

Company rating: 7.4 out of 10

Based on 17 frontline employees who took The Breakroom Quiz


Job description

QC Inspector
Job Locations US-WA-Bothell
Posted Date 1 month ago(8/13/2026 5:54 PM)
Req. # 2026-19421
Job Location : Location US-WA-Bothell
Job Location : Postal Code 98021
Job Location : Address 3350 Monte Villa Parkway
Type Employee
Full Time/Part Time Full Time
Overview
 
As one of the world's leading analytical instrumentation companies, Bruker covers a broad spectrum of advanced solutions in all fields of research and development. All our systems and instruments are designed to improve safety of products, to accelerate time-to-market, and to support industries in successfully enhancing quality of life. We have been driving innovation in analytical instrumentation for over 60 years now. Today, more than 8,500 employees distributed across 90 locations around the world continue to delight our customers with innovative solutions.


Bruker Nano, one of Bruker's four operating segments, provides customers in academic and governmental institutions, life science, materials, and applied industries with the tools to determine the characteristics of matter and visualize the structure of molecules. Divisions within BNANO include Bruker AXS, Bruker Nano Analytics, Bruker Nano Surfaces and Metrology, Fluorescence Microscopy, and Canopy.

The Quality Control Inspector (QCII) is primarily responsible for Quality Control inspections of all Bruker Spatial Biology incoming raw materials, components and sub-assemblies received at our facilities per inspection plan meeting applicable material specifications. QCII is also responsible for all finished instrumentation testing of all final assembled instruments per inspection plan.
 
 
Responsibilities

The scope of this position is includes performing all necessary quality control checks, including FAI's and associated reports (First Article Inspection & Reports), using appropriate testing procedures and test instrumentation supported with appropriate documentation for all Bruker Spatial Biology products to manage quality risk and provide oversight over manufacturing processes. This position reports into the Sr. Quality Manager which is part of Quality organization and support associated tasks and activities coordinated and integrated with production and inventory control. The individual ensures consistent implementation, improvement, and compliance to the Bruker Spatial Biology, ISO 13485 and ISO 9001 Quality Management Systems.

Responsibilities:

  • Perform timely incoming and final quality control inspections to support Manufacturing and Operations quality for all Bruker Spatial Biology instruments following approved and active Incoming Specifications
  • Update incoming inspection specifications and procedures as required, in collaboration with other cross-functional departments.
  • Record non conformances and support in conducting root cause investigations.
  • Manage nonconforming (or potentially nonconforming) material through disposition.
  • Perform lot validation testing while monitoring and adjusting testing frequencies.
  • Support review and updating of SOPs relating to Quality Control Procedures.
  • Collaborate with Manufacturing, Manufacturing Engineering, New Product Introduction, Procurement, Quality, and Supply Chain partners as well as vendors on the above activities.
  • Basic application of statistical tools and methods
  • Participates in FDA/ISO inspections and customer audits and maintain ongoing audit readiness
  • Perform other relevant duties as may be assigned by management
  • Act as Quality ambassador providing decisive approach for implementation to manage Quality Management System with various tasks, projects, as required

Skills and Abilities:

  • Analytical decision-making skills to apply logical or Quality control thinking principles to operations using pragmatic approaches.
  • Demonstrates working knowledge of ISO 9001, ISO 13485 quality system and/or FDA 21 CFR 820 quality regulations as applicable to products.
  • Analytical and creative problem-solving skills that include experience in leading and or participating on process improvement/lean projects.
  • Excellent written and oral communication skills
  • Ability to work independently and collaboratively in cross-functional teams
  • Ability to multi-task with demonstrated problem solving skills in a fast paced complex environment

Specialized Knowledge:

  • GD&T and CMM skills is preferred
  • At least 3 years of experience as a QC inspector in a regulated environment i.e. medical device/ biotechnology/ aerospace industry.
Qualifications

Minimum Education: Bachelor's degree in a related field strongly preferred OR High school STEM or technical diploma or equivalent BS in technical discipline, real world hands-on regulated industry experience may also be considered.

Minimum Experience : 3-5 years quality-related experience in biotech, the pharmaceutical or consumer regulated device industry.

At Bruker, base salary is part of our total compensation. The estimated base salary range for this full-time position is between $41,500 and $66,000 provides an opportunity to progress as you grow and develop within a role. The base salary for the role will depend on a several job-related factors, including, but not limited to education, training, experience, the geographic location of the successful candidate, skills, competencies, job-related knowledge and travel requirements for this position. Full-time employees may also be eligible for a performance-related incentive in addition to a full range of benefits including 401(k) with company match, an employee stock purchase plan, medical and dental plans, life insurance, short-term and long-term disability insurance, employee assistance program and paid time off including vacation, sick time and holidays, and more.

Bruker is an equal-opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

Certain positions at Bruker require compliance with export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine their eligibility in light of export control restrictions

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