Bilingual Quality Assurance

5th HQ; Town of Florida (NY); On-site; USD 21,000 - 29,000; Full time

Job summary

5th HQ is seeking a Quality Assurance Inspector in Miramar, FL, responsible for monitoring, inspecting, and proposing corrective measures to meet quality standards. The candidate should be bilingual in English and Spanish, highly organized, detail-oriented, and able to handle pressure in a fast-paced environment.

Key functions include in-process inspection, cGMP compliance, sampling, testing, and documentation across batch records.

Qualifications

• Associate degree or equivalent in quality control or related field.
• 1-3 years experience in quality control of a manufacturing environment.
• Bilingual English and Spanish required.
• Knowledge in cGMP regulations and FDA guidelines.
• Basic computer and math skills.

Responsibilities

• Performs the inspection of in-process product and gathers the appropriate documentation.
• Ensures cGMP compliance on the production floor at all times.
• Performs QA tasks such as sampling, inspections, and tests to ensure compliance with SOPs, safety initiatives, company policies, FDA and DEA regulations.
• 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 SOPs, cGMPs and FDA/DEA regulations.
• Documents all work activity in batch records, forms, and logs for accuracy and compliance.
• Samples in-process items and finished products, performing required inspections and testing.
• Processes and distributes samples to different departments.
• Reviews cGMP compliance records for accuracy and good documentation practices.
• Applies disposition status to components and in-process materials.
• Issues QA alerts when any questionable component or material is identified.

Skills

Bilingual English and Spanish

Detail oriented

Education

Associate degree or equivalent

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.

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.