Bilingual Quality Assurance Document Control

Quality Assurance (QA) Document Control SpecialistA well-established pharmaceutical company in Miramar, FL is seeking an experienced and detail-oriented Quality Assurance (QA) Document Control Specialist to support its evening shift operations. This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and has prior experience in pharmaceutical or FDA-regulated environments.Location: Miramar, FL Industry: Pharmaceutical Manufacturing Job Type: Full-Time Schedule: Monday to Friday, 2:30 PM – 11:00 PM Pay: $19.00 per hourKey ResponsibilitiesMaintain and control quality documentation in accordance with GMP and FDA guidelinesReview and archive manufacturing, packaging, and testing records for accuracy and completenessEnsure proper version control and distribution of controlled documents (SOPs, batch records, etc.)Assist in audits, inspections, and internal reviews by preparing and providing requested documentationSupport QA team in implementing document changes, updates, and approvalsEnsure timely and accurate entry of documentation into digital or physical filing systemsCollaborate with production, quality, and regulatory departments to ensure documentation complianceReport any deviations or non-conformances found in recordsQualificationsMinimum 1–2 years of experience in document control or QA in a pharmaceutical or FDA-regulated environmentHigh school diploma or equivalent required; associate or bachelor's degree preferredStrong knowledge of GMP, SOPs, and document control best practicesExcellent attention to detail and organizational skillsBilingual (English/Spanish) – requiredProficient in Microsoft Office (Excel, Word, Outlook)Ability to work independently with minimal supervision during evening shift hours