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Remote Iso Document Control Jobs in California (NOW HIRING)

Prismatik

Document Control Specialist

Irvine, CA · On-site +1

$23 - $25/hr

We're looking for a Document Control Specialist to help keep our product development and quality ... Remote or hybrid arrangements are not available. Employment Type: full-time

Verdantas

Project Control Specialist II

San Diego, CA · On-site +1

$65K - $85K/yr

The role is responsible for maintaining project schedules using status updates provided by the project team as well as those conveyed through document control systems. This position is remote.As a ...

DivIHN

IT Project Manager - Remote

San Diego, CA · On-site +1

$104K - $123K/yr

Remote Duration: 18 Months Only W2 candidates are eligible for this position. Third-party or C2C ... Submit, manage and prioritize Change Orders for Document Control Role Overview * Straightforward ...

JenaValve

Senior Manager, Clinical Compliance

Irvine, CA · On-site +1

$160K - $170K/yr

Remote - Home Office Summary: Reporting to the Vice President, Clinical Affairs, the Senior Manager ... document control processes and procedure governance. * Monitor and communicate regulatory ...

Cleanwater1, Inc

Lead Control System Engineer

Ripon, CA · Remote

$98K - $120K/hr

Define functional requirements through client workshops, site assessments, and documentation ... Design, configure, and support remote access and telemetry solutions using Ethernet, industrial ...

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Remote Iso Document Control information

What is the difference between Remote Iso Document Control vs Remote Quality Document Control?

AspectRemote Iso Document ControlRemote Quality Document Control
CertificationsISO standards knowledge, document management certificationsQuality management system certifications, document control certifications
Work EnvironmentPrimarily office or remote, industry-specificPrimarily office or remote, industry-specific
Industry UsageManufacturing, engineering, aerospaceManufacturing, healthcare, automotive
Search & ComparisonOften compared for ISO compliance rolesCompared for quality assurance roles

Remote Iso Document Control focuses on managing documents related to ISO standards compliance, ensuring proper documentation for certifications and audits. Remote Quality Document Control emphasizes maintaining quality management system documents across various industries. While both roles involve document management, Iso Document Control is more specialized in ISO standards, whereas Quality Document Control covers broader quality processes.

What are popular job titles related to Remote Iso Document Control jobs in California? For Remote Iso Document Control jobs in California, the most frequently searched job titles are:
What job categories do people searching Remote Iso Document Control jobs in California look for? The top searched job categories for Remote Iso Document Control jobs in California are:
What cities in California are hiring for Remote Iso Document Control jobs? Cities in California with the most Remote Iso Document Control job openings:
Remote Iso Document Control jobs near you

Document Control Specialist

Prismatik

Irvine, CA • On-site, Remote

$23 - $25/hr

Full-time

Re-posted 4 days ago

Job description

We're looking for a Document Control Specialist to help keep our product development and quality systems running smoothly.

You'll manage the documents that support our products throughout their lifecycle-ensuring they're accurate, compliant, and available when teams need them. Working closely with Engineering, Quality, Regulatory, and Manufacturing, you'll help drive document reviews, change requests, training records, and quality system processes that keep product development on track.

Essential Functions:

  • Maintains all Engineering and Product Development records to ensure integrity and accessibility including but not limited to photocopying and scanning documents.
  • Processes and controls storage of Quality Records.
  • Interacts directly with users of controlled documentation to ensure internal conformance to company quality control requirements.
  • Processes review and approval workflows in electronic document management system.
  • Reviews document format to ensure compliance to Good Documentation Practices (GDPs).
  • Assists in Food and Drug Administration (FDA) inspections and Notified Body audits regarding marketed products, as requested.
  • Tracks and facilitates timely documentation review and implementation.
  • Distributes documents in accordance to control procedures.
  • Ensures accurate and timely input of database entries; implements a self-auditing system to verify work.
  • Analyzes change requests for completeness.
  • Provides support to internal customers with documentation needs.
  • Updates electronic document profiles to reflect appropriate changes.
  • Provides clerical and administrative support related to documentation processes and systems.
  • Creates and maintains document templates by coding fields and uploading into the electronic document management system.
  • Routes and releases documentation.
  • Follows up on training requirements to ensure compliance to the department's standard operating procedures.
  • Assists with monitoring the Document Control email inbox to ensure all requests are assigned and responded to in a timely manner. Communicates among the Document Control team to ensure request are fully completed.
  • Maintains the document archival room; ensures files are accurate and easily retrievable.
  • Assists with training program by filing training records and logging training.
  • Works with a variety of internal teams to ensure receipt of training materials.
  • Performs other related duties and projects as business needs require at direction of management.

Minimum Qualifications

  • High school diploma or equivalent.
  • Minimum two (2) years of experience in dental or medical device industry.
  • Minimum one (1) year of customer service experience.
  • Proficient skills in the MS Office Suite (Word, PowerPoint, and Outlook); advanced proficiency in Excel.
  • Demonstrated knowledge of document control fundamentals, quality systems, and Good Manufacturing Practice (GMP) requirements.
  • Demonstrated understanding of current medical device industry and applicable regulations.
Pay range: $23.00 to $25.00/hr
Exact compensation may vary based on skills and experience.
This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.
Employment Type: full-time

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