Quality Control Document Specialist5TH HQ LLC • Fort Lauderdale, FL, US
Quality Control Document Specialist
5TH HQ LLC • Fort Lauderdale, FL, US
[job_card.variable_days_ago]
[job_preview.job_type]
- [job_card.full_time]
[job_card.job_description]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
Job Description
Job Description
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 :
- 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
Key Responsibilities :
Preferred Skills :
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