Bilingual Quality Inspector (Eng/Spa) Position Available In Broward, Florida
Tallo's Job Summary: We are looking for a Bilingual Quality Inspector (Eng/Spa) in Miramar, FL, offering full-time hours and a salary range of $17 - $19 an hour. The role requires bilingual proficiency in English and Spanish, knowledge of CGMP regulations, and experience in quality control within a manufacturing setting. The inspector will be responsible for monitoring, inspecting, and proposing corrective measures to ensure final products meet quality standards.
Job Description
Bilingual Quality Inspector (Eng/Spa) 5th
HQ – 5.0
Miramar, FL Job Details Full-time $17 – $19 an hour 6 hours ago Qualifications Bilingual Spanish CGMP English Mid-level High school diploma or GED Quality control Computer skills 1 year Manufacturing Associate’s degree FDA regulations Full Job Description 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.
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.
