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Bilingual Quality Assurance5th HQ • Florida, New York, United States
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Bilingual Quality Assurance

5th HQ
  • US
    Florida, New York, United States
  • US
    Florida, New York, United States
Jetzt Bewerben

Über

5th HQ We're seeking for a Quality Assurance Inspector in Miramar, FL. who will be responsible for monitoring, inspecting and proposing measures to correct or improve final products in order to meet established quality standards. The ideal candidate must have a very positive attitude, energetic, very organized, detailed orientated, handle pressure well, and excel in a fast paced and highly dynamic environment. Must be fully bilingual English- Spanish.
Schedule: 6am-2:30pm or 2:30pm-11pm
Salary $18
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES
Performs the inspection of in-process product, and gathering the appropriate documentation
Assures cGMP compliance at all times on the production floor
Performs Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP's, Safety initiatives, Company policies, FDA and DEA regulations documenting all work performed, ensuring accuracy and thoroughness informing management of any deviations from established internal and regulatory standards/procedures
Inspects and approves rooms, lines and equipment prior to use by manufacturing and R&D personnel
Approves components for in-process operations
Monitors manufacturing and packaging areas for compliance with internal SOPs, cGMPS and FDA/DEA regulations
Documents all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance
Samples in-process items, and finished products, performing required inspections and testing of in-process items and finished products.
Processes and distribute samples to different departments
Reviews cGMP compliance records for accuracy and thoroughness and good documentation practices.
Applies disposition status to components and in-process materials
Issues QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage
QUALIFICATIONS
Associate degree or equivalent work experience
1-3 years experience in quality control of a manufacturing environment
Bilingual (English and Spanish) required
Knowledge in cGMP regulations and FDA guidelines
Detailed oriented
Basic computer and math skills.
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  • Florida, New York, United States

Sprachkenntnisse

  • English
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