- Responsible for performing the inspection of in-process product, and the appropriate documentation
- Assures cGMP compliance all at times in the production floor
- Perform 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. Document all work performed, ensuring accuracy and thoroughness. Inform management of any deviations from established standards/procedures
- Inspect and approve rooms, lines and equipment prior to use by manufacturing and R&D personnel
- Approve components for in-process operations
- Monitor manufacturing and packaging areas for compliance with internal SOPs, cGMPS and FDA/DEA regulations
- Document all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance
- Sample in-process items, and finished products. Perform required inspections and testing of in-process items and finished products. Process and distribute samples to different departments
- Review records for cGMP compliance for accuracy and thoroughness and good documentation practices.
- Inform management of problems, failures and deviations from established internal and regulatory standards
- Apply disposition status to components and in-process materials
- Issue QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage
- Any other required duties assigned by the immediate supervisor
- 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
About the company
Company website•Pharmaceutical Manufacturing
Established in 1972, Arnet Pharmaceutical has researched, manufactured and marketed natural products worldwide. Arnet Pharmaceutical is an internationally recognized contract manufacturer known for its quality and service. Actively, Arnet serves over 70 countries around the world. Our Quality Assurance department works closely with each customer to guarantee compliance and the necessary documentation needed to meet the most stringent standards.
Arnet Pharmaceutical is housed in a 130,000 sq. ft., all air conditioned, space in Davie Florida with 350 employees. Our facility includes offices, laboratory, manufacturing and warehouse areas and includes separate rooms for our production machinery. Arnet’s extensive line of products includes a complete range of vitamins, minerals, amino acids and herbal supplements. Arnet also has the capability to do: Tablets, Capsules, Powders and Chewables.
Over the years, Arnet Pharmaceutical has led the nutritional supplement industry in price, quality and innovation. We have built lasting and profitable relationships with our private label customers. Arnet Pharmaceutical is a modern, efficient, full service private label contract manufacturer of nutritional supplements, vitamins, minerals, herbal products, specialty products and diet aids.
We provide you with only the highest quality products from the finest ingredients. All formulas are manufactured under the guidelines of:
– United States Pharmacopoeia (U.S.P.)
– Current Good Manufacturing Practices (c.G.M.P.)
– Standard Operating Procedures (S.O.P.)
– Disintegration, potency and dissolution are guaranteed
– FDA Registered Facility and Labeler code for Customers
Our commitment to quality assures you that our customers will be provided with the most effective formulations produced under strict quality control standards. Our guarantee is that Arnet Pharmaceutical will always stand behind its products.