Production Manager
Treat Pharmaceutical Industry Pvt; Ltd. (Bannu. K.P
مجموع سنوات الخبرة :14 years, 1 أشهر
for data management, analyzing performance, identifying problems, and developing recommendations that support supply chain/logistics management
•Establishes checkpoints on work-in-progress to guarantee accuracy of work performed. Communicates issues to plant personnel, sales department and customer
•Works closely with the Materials Supervisor, Engineering Project Leads, Build Managers, Procurement, Sales and Senior Management to manage schedules
that experiments are completed according to established Standard Operating Practices (SOP), Good Laboratory Practices (GLP) as well as any applicable federal regulations or industry standards.
•Communicates with production manager and other employees within factory to resolve Q.A/Q.C issues in a proactive manner.
•All Raw Materials are tested on site before use, Incoming identity, Full release testing, Includes Excipients, Capsules, API, Assay (HPLC, FT-IR, UV-Vis; and Titration) and Physical Tests.
•All packaging components tested if in contact with drug product Bottles Blister pack components Cotton wool, Desiccants, Range of techniques, Appearance, Spectroscopy, Loss on Drying.
•Finished Product before release into market, HPLC and Dissolution, Content Uniformity, Dissolution %, Dissolved Time.
•Scheduled reassessment of released drugs, Ensures continued efficacy, Release HPLC, Dissolution, Reassay schedule drug dependant Comparators - manufacturers expiry. In house drugs - decided by formulator.
•Able to read interpret and fully understand formulations and specifications.
•Verify materials, parts and final products through independent checks, audit inspections and witnessing.
•Comply with all relevant quality standards and regulations.
•Review of the formulation specifications and specified standards to assure compliance with the applicable regulatory requirements.
•Review of specifications, procedures and specified standards utilized on production area.
all quality control operations, including making team assignments, providing support to junior QC analysts, and completing annual performance reviews.
•Develop comprehensive quality control requirements and procedures for each project, including product sample rates, QC rating scales, and flowcharts for solving production issues.
•Collate all QC data from quality assurance personnel, and create detailed production reports for project managers and clients.
•Interface directly with clients to determine appropriate QC requirements prior to production run, provide quality assurance information throughout production, and ensure customer satisfaction at project completion.
•Perform quarterly testing and optimization analysis on QC equipment to ensure correct operational performance and results.
Successfully Developed Graphene Nano-sheets by Techniques: “Electrochemical Exfoliation & successive Reduction by Microwave.” 2011 ─ 20
•Synthesized the Graphene Nano-sheets from Graphite.
•Characterized of developed product (Graphene Nano-sheets) by SEM, AFM, EDX, TGA, XRD, ATR, UV-Vis, Surface area analyzer and its performance by Potentiostate
Prepared and characterized the Mesophase from petroleum pitch. 2012 ─ 13
•Studied the carbonization process of petroleum pitch through dehydrogenation condensation polymerization in a flow of N2 atmosphere.
•The yield calculated at varying temperature and pressure.
•FT-IR, SEM, X-ray diffraction and optical microscopy used to confirm the graphitization of the carbonized petroleum pitch.
Biosorption of Methylene Blue by Low-cost Biosorbents. 2013 ─ 14
•Saccharum arundinaceum used as Novel biosorbent
•Characterized the biosorbate & Biosorbents by ATR and UV-Vis
•Optimized the sorption conditions
•Study of sorption Kinetics, Applied the Isotherms and Error functions
, K.P.
in
Concentration-
.