Conductor de montacargas

Conductor de montacargas

Tipo de contrato:

contrato

Ubicación:

Albert Park - Victoria

Industria:

categoría

Nombre de contacto:

nombre de contacto

Email de contacto:

correo electrónico de contacto

Fecha de publicación:

05-mayo-2023

The JobSquad Solutions Team is currently looking for a Quality Assurance Document Specialist to work at a company located in the Miramar, FL area!
Job Title





Quality Assurance Document Specialist – Nutraceutical Industry
Position Location




Miramar, FL 
 
Pay/hours for position





Hours are Monday-Friday 8:30AM-5:00 PM
$18-22 hourly
 
 
 
 
Requirements of position




Education & Experience
  1. Associate’s or Bachelor’s Degree preferred (Life Sciences, Chemistry, Biology, Quality Management, or related field).
  2. 1–3 years of experience in QA or Document Control within the nutraceutical, pharmaceutical, food, or related regulated industry.
  3. Familiarity with cGMP, FDA 21 CFR Part 111/117, and quality documentation systems.
Skills
  1. Strong attention to detail and accuracy.
  2. Excellent organizational and time-management skills.
  3. Knowledge of Good Documentation Practices (GDP).
  4. Proficiency in Microsoft Office (Word, Excel, Outlook).
  5. Experience with electronic document management systems (EDMS) is a plus.
  6. Strong communication skills (written and verbal).
Work Environment
  1. Office-based position with regular interaction with production, QC, warehouse, and QA leadership.
  2. May require occasional presence in manufacturing areas to verify documentation or support audits.
Schedule
  1. Full-time, Monday–Friday (hours vary by facility).
Physical Requirements
  1. Ability to sit or stand for extended periods.
  2. Ability to lift up to 20 lbs for handling document boxes or files.
 
Responsibilities of position





 Documentation Control
  1. Maintain, review, and update controlled documents such as SOPs, Batch Production Records (BPRs), Specifications, MMRs, Forms, Logs, and QA Policies.
  2. Ensure all documents comply with FDA 21 CFR Part 111/117, cGMP guidelines, and internal quality systems.
  3. Issue controlled documents to Production, QC, and other departments as needed.
  4. Manage document revision requests, approval workflows, and document obsolescence.
Record Management
  1. Review completed batch records for accuracy, completeness, and compliance before final QA release.
  2. Maintain digital and physical filing systems for quality and production records.
  3. Ensure traceability and proper archival of all quality documents according to retention requirements.
Quality Assurance Support
  1. Assist in internal audits by preparing necessary documentation.
  2. Support external audits (FDA, NSF, UL, third-party) by organizing and presenting required records.
  3. Monitor adherence to proper documentation practices (GDP) across departments.
Process Improvements
  1. Identify documentation gaps and recommend corrective actions.
  2. Support the development of new documentation templates and workflows.
  3. Participate in continuous improvement initiatives relating to quality systems.
The JobSquad Solutions Team is made up of experts around the country. Serving our local workforce communities is our passion.
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