5TH HQ LLC
A 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 hour
Key Responsibilities
Maintain and control quality documentation in accordance with
GMP
and
FDA
guidelines Review and archive manufacturing, packaging, and testing records for accuracy and completeness Ensure proper version control and distribution of controlled documents (SOPs, batch records, etc.) Assist in audits, inspections, and internal reviews by preparing and providing requested documentation Support QA team in implementing document changes, updates, and approvals Ensure timely and accurate entry of documentation into digital or physical filing systems Collaborate with production, quality, and regulatory departments to ensure documentation compliance Report any deviations or non-conformances found in records Qualifications
Minimum 1-2 years of experience in
document control or QA
in a
pharmaceutical or FDA-regulated environment High school diploma or equivalent required; associate or bachelor's degree preferred Strong knowledge of
GMP, SOPs , and document control best practices Excellent attention to detail and organizational skills Bilingual (English/Spanish)
- required Proficient in Microsoft Office (Excel, Word, Outlook) Ability to work independently with minimal supervision during evening shift hours
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 hour
Key Responsibilities
Maintain and control quality documentation in accordance with
GMP
and
FDA
guidelines Review and archive manufacturing, packaging, and testing records for accuracy and completeness Ensure proper version control and distribution of controlled documents (SOPs, batch records, etc.) Assist in audits, inspections, and internal reviews by preparing and providing requested documentation Support QA team in implementing document changes, updates, and approvals Ensure timely and accurate entry of documentation into digital or physical filing systems Collaborate with production, quality, and regulatory departments to ensure documentation compliance Report any deviations or non-conformances found in records Qualifications
Minimum 1-2 years of experience in
document control or QA
in a
pharmaceutical or FDA-regulated environment High school diploma or equivalent required; associate or bachelor's degree preferred Strong knowledge of
GMP, SOPs , and document control best practices Excellent attention to detail and organizational skills Bilingual (English/Spanish)
- required Proficient in Microsoft Office (Excel, Word, Outlook) Ability to work independently with minimal supervision during evening shift hours