Bilingual Quality Control Document Specialist at 5th HQ
Miramar, Florida, USA -
Full Time


Start Date

Immediate

Expiry Date

11 Oct, 25

Salary

20.0

Posted On

11 Jul, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Microbiology, Biology, Regulatory Requirements, Data Systems, Microsoft Office

Industry

Pharmaceuticals

Description

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

PREFERRED SKILLS:

  • 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
Responsibilities
  • 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
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