Documents Control Specialist
$70,000–$80,000 year
On-site · San Diego, California, United States
San Diego, California, United StatesOn-siteFull Time$70,000–$80,000 yearMid LevelNot SpecifiedUnknown
Type
Full Time
Level
Mid Level
Education
Not Specified
Company size
Unknown
Job Summary
Document Control Specialist to maintain quality documentation for cGMP compliance in a San Diego-based supplement manufacturer; create/revise/archive controlled documents (MMRs, BPRs, SOPs, specs, forms); manage document change control; support audits and FDA inspections; ensure GDP/data integrity; train staff on document control and GDP.
Required Qualifications
- 3+ years document control experience in supplements, food, or pharma (supplements preferred)
- Strong knowledge of FDA 21 CFR Part 111 (MMRs, BPRs, recordkeeping)
- Experience with specification sheets and GDP/data integrity
- Detail-oriented with strong organizational and communication skills
- Proficient in Microsoft Office; QMS experience a plus
- FDA inspection or GMP audit support experience (NSF, UL, etc.)
- Familiarity with CAPA and change control systems
- Experience in small-to-mid-size manufacturing environments
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