GMP Document Control Specialist - Hybrid CAR-T Ops

Talentify

Newark (CA)

Hybrid

USD 65,000 - 90,000

Full time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Benefits offered by this job

Medical, dental, vision
Retirement options

Job summary

TalentBurst is seeking a detail-oriented Document Control Specialist to join our Quality team at the Newark, CA facility. This role supports controlled-document lifecycle activities across production, validation, testing, and quality operations in a GMP-regulated environment.

The ideal candidate has 5+ years of document control experience, strong skills in Word/Excel/Adobe Acrobat/Visio, and familiarity with Veeva QualityDocs.

Qualifications

  • High school diploma required with minimum 5 years' document control experience in GMP-regulated pharma/biologic/medical device environments.
  • Experience with controlled-document lifecycle in production, validation, testing and quality operations.
  • Familiarity with electronic document management systems (EDMS) like Veeva QualityDocs and strong MS Office proficiency.

Responsibilities

  • Provide responsive support to internal customers to promote timely project execution and a positive customer experience.
  • Partner with internal customers to create and revise procedures and execution documents aligned with processes and timelines.
  • Process, distribute, and maintain GMP documentation including production, testing, validation, and quality records.

Skills

Attention to detail
Organizational skills
Communication
Cross-functional collaboration

Education

High school diploma

Tools

Veeva QualityDocs
Microsoft Word
Microsoft Excel
Adobe Acrobat
Visio

Job description

TalentBurst is seeking a detail-oriented Document Control Specialist to join our Quality team at the Newark, CA facility. This role supports controlled-document lifecycle activities across production, validation, testing, and quality operations in a GMP-regulated environment.

The ideal candidate has 5+ years of document control experience, strong skills in Word/Excel/Adobe Acrobat/Visio, and familiarity with Veeva QualityDocs.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Document Control Specialist
Document Control Specialist

Talentify • Newark (CA)

Hybrid
USD 65,000 - 90,000
Medical, dental, vision
Retirement options
GxP Document Control Specialist — Hybrid
GxP Document Control Specialist — Hybrid

Actalent • Boston (MA)

Hybrid
USD 34,000 - 39,000
Veeva Document Control & GMP Specialist
Veeva Document Control & GMP Specialist

Actalent • United States

Hybrid
USD 41,000 - 52,000
Medical, dental & vision
401(k) Retirement Plan
Life Insurance
+2
Quality & Document Control Specialist
Quality & Document Control Specialist

Nucleus Biologics • San Diego (CA)

On-site
USD 60,000 - 85,000
Senior Document Control Specialist - Hybrid QA & Compliance
Senior Document Control Specialist - Hybrid QA & Compliance

Personalis, Inc. • Fremont (CA)

Hybrid
USD 54,000 - 61,000
Hybrid schedule
GMP Document Control Specialist
GMP Document Control Specialist

THG • New Jersey

On-site
USD 60,000 - 70,000
GMP Document Control Lead - Inspection Ready
GMP Document Control Lead - Inspection Ready

Emergent Biosolutions • Canton (MA)

On-site
USD 129,000 - 156,000
Quality Document Control Specialist
Quality Document Control Specialist

Nephron Pharmaceuticals Corporation • West Columbia (SC)

On-site
USD 42,000 - 64,000
Quality Systems Document Control Specialist
Quality Systems Document Control Specialist

Talentify • Minneapolis (MN)

On-site
USD 41,000 - 48,000
Medical/dental/vision
401(k) Retirement Plan
Life Insurance
+2
GMP Document Control Specialist
GMP Document Control Specialist

The Hut Group • New Jersey

On-site
USD 60,000 - 70,000