Associate Specialist, Quality Assurance

Job description

WHERE YOU WILL WORK: Without compromising our steadfast commitment to Quality, Safety and Sustainability our manufacturing and packaging facility produces in excess of 70MM units per year. This is a demonstration of our can-do attitude, collaborative spirit, focus on innovation and continuous improvement mindset. Always People First! JOB SUMMARY: The Quality Assurance Associate Specialist is responsible for preparing and completing the CARES act report for FDA, is responsible for BOM review and approval, Bulk and Finished Good, Responsible for Releasing Finished Goods (OTC, Non-OTC etc.) reviewing Batch records, specifications, procedures, protocols, and records for GMP compliance. WHAT YOU WILL DO: - You will prepare and complete the CARESS ACT list for FDA. - You will complete BOM review and approval, set up the system specifications for Finished Goods, FG, and Bulk working closely with different departments - You will be responsible for Releasing Finished Goods (OTC, Non-OTC, etc.) - You will prepare master production records for all OTC products. - You will review raw material, packaging material, in-process material and finished product specifications for GMP compliance – Reco...