Top 7 Document control specialist Jobs in Fremont, Ca

Sr. Document Control Specialist (Temp - 3 Month)
Personalis, Inc —Fremont, CA
- $39 - $44 an hour
- Temporary
- Google Workspace
- Microsoft Excel
- Mid-level
3d
Document Control Specialist
Springtide Project Services —Santa Clara, CA
- $77,000 - $118,000 a year
- Full-time
- Construction site
- Ability to walk for extended periods
- 5 years
ISO / Document Control Specialist
Foxconn Industrial Internet —San Jose, CA
- $28 - $32 an hour
- Full-time
- Writing skills
- Mid-level
- Agile
Quick Apply
13d
Configuration and Data Management Specialist
Archer —San Jose, CA
- $110,000 - $145,000 a year
- Email
- Mid-level
- Agile
- Leadership
Quick Apply
Senior PLM Specialist
Mytra —Brisbane, CA
- $115,000 - $140,000 a year
- Full-time
- Engineering
- Office
- Product management
- Commuter assistance
- Paid holidays
Quick Apply

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Sr. Document Control Specialist (Temp - 3 Month)
Personalis, Inc —Fremont, CA
Operating with minimal supervision, the ideal candidate brings strong expertise in document control within regulated environments (e.g., ISO 13485, 21 CFR Part…
$39 - $44 an hour
3d
Document Control Specialist
Springtide Project Services —Santa Clara, CA
The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research,…
$77,000 - $118,000 a year

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Coordinate document delivery to meet project schedule and working with Project team/Procurement Lead to ensure the need by dates of documents meet schedules for…

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Sr. Document Control Specialist (Temp - 3 Month)

Personalis, Inc -
Fremont, CA

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Job Details

Temporary
$39 - $44 an hour
3 days ago

Qualifications

Technical editing
Google Workspace
Microsoft Excel
Technical documentation
ISO standards
Regulatory compliance
Biomedical regulatory compliance
Document viewing software
Technical writing quality assurance
Technical writing experience within technology
Cross-functional collaboration
Adobe Acrobat
Cross-functional communication
FDA regulations

Full Job Description

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California.

Hybrid: Mon & Tues

Summary:

The Sr. Document Control Specialist (Temp) will serve as a key member of the Quality Assurance team, maintaining daily document control operations across the organization. Operating with minimal supervision, the ideal candidate brings strong expertise in document control within regulated environments (e.g., ISO 13485, 21 CFR Part 820). This role reports directly to the Director, Quality Assurance.

Responsibilities:

Document Change Order (DCO) Management: Triage, review, re-format, proofread, and process DCOs through the electronic document management system (EDMS) to ensure clarity, consistency, and compliance with internal and external quality standards.
Cross-Functional Collaboration: Partner with change initiators and reviewers across departments to resolve DCO discrepancies and expedite approval workflows to meet turnaround times.
Quality Records & System Integrity: Meticulously control, file, and maintain accessibility of Quality System documentation, master signature logs, data, and records inventory.
Periodic Reviews & Tracking: Facilitate periodic document reviews, follow up on past-due items, and escalate system issues or bottlenecks as needed.
General QA Support: Manage multiple document projects simultaneously and perform additional document control and QA support duties as assigned.

Education & Experience Requirements:

Education: Bachelor's degree or equivalent experience in a document control capacity.
Experience: 3+ years of experience in document control within a regulated medical device, IVD, or pharmaceutical environment.
Systems: Hands-on experience with Electronic Document Management Systems (EDMS). Experience with ComplianceQuest (CQ) is a plus.
Regulatory Knowledge: Sound working knowledge of ISO 13485 and FDA 21 CFR Part 820 requirements.

Skills & Competencies:

Attention to Detail: High precision in proofreading, formatting, and verifying document compliance against established templates and requirements.
Independence & Prioritization: Proven ability to work independently, prioritize competing tasks, and manage workload in a fast-paced environment.
Communication & Technical Writing: Strong written and verbal communication skills with a customer-service orientation when collaborating across all organizational levels.
Software Proficiency: Advanced skills in Microsoft Office (Word, Excel, PowerPoint), Adobe Acrobat, and Google Workspace.

The hiring range for this position is $39.00 to $44.00 per hour, which may factor in various geographic regions.

Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know, if/when they contacts you.

Personalis is an Equal Opportunity Employer/Minorities/Females/Veterans/Disabilities.

#LI-JT1 #LI-Onsite

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document control specialist jobs in fremont, ca

Sr. Document Control Specialist (Temp - 3 Month)

Document Control Specialist

ISO / Document Control Specialist

Configuration and Data Management Specialist

Senior PLM Specialist

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