5TH HQ LLC
Bilingual Quality Assurance Document Control
5TH HQ LLC, Fort Lauderdale, Florida, United States, 33324
Job Description
Job Description
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
Job Description
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