Quality Control Document Specialist
5TH HQ LLC
Job Title: Quality Control Document Specialist
Location: Miramar, FL
Department: Quality Assurance / Regulatory Affairs
Employment Type: Monday - Friday 8:30am - 5pm $20/ HR We are currently seeking a Quality Control Document Specialist with a strong background in microbiology to support our Quality Control Department. This position plays a key role in ensuring compliance with regulatory standards and maintaining a clean, safe, and efficient laboratory environment. MUST BE BILINGUAL ENGLISH/SPANISH Minimum Qualifications:
Location: Miramar, FL
Department: Quality Assurance / Regulatory Affairs
Employment Type: Monday - Friday 8:30am - 5pm $20/ HR We are currently seeking a Quality Control Document Specialist with a strong background in microbiology to support our Quality Control Department. This position plays a key role in ensuring compliance with regulatory standards and maintaining a clean, safe, and efficient laboratory environment. MUST BE BILINGUAL ENGLISH/SPANISH Minimum Qualifications:
- Bachelor's degree in Microbiology, Biology, Biomedical Science, or a related field required; Master's degree preferred
- Minimum of 1 year of experience in a microbiology laboratory within a cGMP-regulated manufacturing environment
- Solid understanding of microbial techniques and methodologies to monitor bacteria, fungi, and other microorganisms
- Familiarity with regulatory requirements and documentation protocols in a laboratory setting
- Follow all procedures and processes to ensure compliance with current Good Manufacturing Practices (cGMP)
- Conduct daily monitoring of microbial cultures in the microbiology laboratory
- Perform laboratory testing and analyses as assigned, including testing of raw materials, finished products, and water samples
- Review analytical assay data for accuracy and compliance; determine acceptability of results
- Inspect manufacturing equipment and personnel for potential sources of contamination
- Support root cause analysis and investigations for out-of-specification (OOS) results
- Maintain clear, organized, and accurate documentation of lab procedures and test results
- Ensure that all work meets established timelines and client or regulatory requirements
- Collaborate with other departments to identify and resolve technical issues
- Contribute to the development and maintenance of safety and compliance standards within the lab
- Provide additional support to the Quality Control Manager as needed
- Strong attention to detail and documentation accuracy
- Effective communication and collaboration skills
- Ability to work independently and prioritize tasks in a fast-paced environment
- Proficient in Microsoft Office and laboratory data systems
Vacancy posted 1 day ago
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