Monitoring the production processes done by the contract manufacturing partner companies. Cooperating with the regulatory affairs department to outsource the PMQC of products. Analysing problems encountered in the manufacturing of the products. Reviewing and analysing analysis sheets, BOM, and batch records. Cooperating with the R&D department to troubleshoot and modify product formulations and to scale up new products. Cooperating with the R&D department. Establishing effective communication with the contract manufacturing partner. pharmaceutical companies for the necessary coordination. Writing and editing the required SOPs and instructions. Requirements: Familiarity with pharmaceutical forms of tablets, capsules, softgels, syrups, suspensions, sachets, and nasal sprays. Ability to manufacture and troubleshoot related devices and machinery. Experience working in pharmaceutical factories, preferably on production lines. Familiarity with QC and IPQC in the pharmaceutical industry. Familiarity with the scale-up of pharmaceutical products. Relative familiarity with GMP in the pharmaceutical industry and related standards. Familiarity with the contract manufacturing process.