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Therapiva Pharma | Walk-in interview for Production - QA | 27 July 2019 | Hyderabad

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    Date: 27th July 2019
    Time: 9:30 AM to 4:00 PM 


    Venue : 
    Therapiva Private Limited 
    Plot # 218 & 219, Phase II,
    IDA Pashamylaram,Sangareddy,
    Telangana.
    Landmark: Beside Biocon Ltd.

    Production Chemists 

    Job Role: Production Chemists 
    Experience: 1 to 4 yrs
    Location: Hyderabad
    Qualification: B.Sc/M.Sc

    Key Responsibilities: 

    • Responsible for day to day shift activities and report to Executive (or) Shift In charge.
    • Responsible to maintain Good housekeeping in production block and surrounding areas of the production area.
    • All documents like batch manufacturing and control records, cleaning records, equipment log books, housekeeping and weighing balance checklists etc to be maintained online.
    • Manufacturing the drug products as per Batch Production and Control Records (BPCR) and performing process operations as per standard operation procedure.
    • To check all the labels before batch charging.
    • Any deviation (or) abnormality observed to be intimated to the executive (or) shift in charge.
    • Responsible to follow safety instructions given in batch manufacturing and control records.
    • Responsible to attend cGMP, Safety and other trainings conducted.
    • Responsible to guide casual helpers to get the work in safe manner.

    QA 

    Job Role: QA Chemists
    Experience: 2 to 6 years 
    Location: Hyderabad
    Qualification: M.Sc.(Chemistry)

    Key Responsibilities :

    • Review of BPCRs in line with technical package received for various projects from R&D centre.
    • Review and approval of executed BPCRs received from manufacturing department related to various projects.
    • Organizing and imparting trainings for various training programs.
    • Checking online operations in concerned departments for ensuring GMP compliance.
    • Handling and review of deviations and change controls related to concerned departments.
    • Handling of customer complaints.
    • Handling of OOS.
    • Reviewing and approval of concerned department SOPs.
    • Preparation, Review and approval of quality assurance SOPs.
    • Preparation, Review and approval of Purified water system protocol, data and report.
    • Online monitoring of purified water system for compliance.
    • Review and approval of AHU protocols, data and report.
    • Preparation, Reviewing and approval of cleaning validation protocols.
    • Review and approval of process validation protocols and reports.
    • Reviewing and approval of equipment qualification protocols and reports.
    • Handling of internal audits.
    • Identification of various procedures related to concerned departments for effective quality system implementation.
    • Vendor qualification management.
    • Facilitate during customer / regulatory audits by coordinating with Head-QA.
    • Release of API / Intermediate.
    Interested candidates can send their updated resume to ranjit.nalbothu@therapiva.net or hr@therapiva.net.

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