- 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
- 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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Quality Control - Miramar, United States - 5th HQ
Description
5th HQ -
Currently seeking a meticulous and dedicated Quality Control Inspector to join our team. The ideal candidate will play a critical role in ensuring our products meet the highest quality standards. This position involves inspecting in-process products, conducting various quality assurance tasks, and monitoring compliance with internal SOPs, cGMP regulations, and FDA guidelines.
Responsibilities:
Qualifications:
Other: Work schedule is Friday, Saturday and Sunday 6am to 6pm .
Physical Requirements:
Works frequently in a manufacturing and lab environment, requires standing, bending, lifting, handling of chemicals and use of monitors and computers. Must be able to wear appropriate PPE such as face masks, respirator, goggles and earplugs.
Typical Work Conditions
Subject to food and nutritional bulk ingredients, which may affect the respiratory system or the skin, including an environment subject to odors, dust or airborne allergens. Person will be working in a dry and low moisture environment and will be exposed to normal work hazards, including a variety of physical conditions such as a proximity to moving mechanical parts. Exposure to noise.
