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Hikal Pharma | Walk-in interview for QA/QC | 15th to 20th April 2019 | Bangalore


    Officer Position : Looking for QC Officers having hands on experience in HPLC & GC. Preferring candidates who can join immediately or at the earliest & who is ready to come in shifts. 

    Qualification - M.Sc/ B.Sc - Chemistry- General / Industrial/ Organic /Inorganic/ Analytical/M.Pharma/ B.Pharma

    Experience :- 2.5 - 5 Years of experience in bulk drug / API in quality control department

    Job Responsibility :

    1 Analysis of samples by chemical method and online reporting of in process and intermediate samples and analysis of in process validation samples.
    2 Analysis of samples by Instrumental methods using HPLC, GC, FTIR, UV-VIS, Malvern master sizer, Potentiometric technique.
    3 Thorough knowledge on handling of HPLC, GC, FTIR, UV-VIS, Malvern master sizer, Potentiometric techniques.
    4 Knowledge on handling of OOS, Deviations, Incidents.
    5 Exposure to regulatory audits.
    6 Analysis of rinse and swab samples.
    7 Preparation and maintenance of reagents and volumetric solutions.
    8 Exposure to analytical method validation using HPLC, GC and IC

    QA Officer Position :Having experience of IPQA  or AQA (QC documents review). Preferring candidates who can join immediately or at the earliest. Also candidates should be ready to work in shifts. 

    Qualification - M.Sc Chemistry- General / Industrial / Organic / Inorganic / Analytical/B. Pharma, M.Pharma

    Experience :- 2.5 - 6 Years of experience in bulk drug / API in QA department in IPQA Team & QC documents Review Team.

    Job Responsibility :

    A. FOR IPQA Role :

    1. To review/ monitor the in-process QA activities at site.
    2. Plant surveilliance, contemporaneous recording and GMP compliance in shifts.
    3. Review of GMP documents (BPCR/Analytical
    documents etc.)
    4. Prepare the gap analysis and compliance report.
    5. Co-ordination for Deviation / Change control /
        OOS with cross functional departments.
    6. Document /SOP preparation /Validation review.
    7. Review and update the investigations for QMS.

    B. FOR AQA Role :

    1.Review the analytical documents in chromatographic system in     view of data integrity.
    2. Review and update the investigations for QMS.
    3. Review of analytical documents related to AMV, AMT,
    in-process, intermediate, cleaning, PRF, Stability etc.
    4. Prepare the gap analysis and compliance report.
    5. Co-ordination for Deviation/Change control /
    OOS/LIR with QC department.
    6. Hands on experience in HPLC, GC & other QC instruments.

    Walk in interview are scheduled from 15th to 20th April '2019  timings are from 09:00 AM - 01:00 PM only

    Documents required at the time of Interview: 
    Updated resume
    Current Employer appointment letter / Increment letter
    Last 3 months salary slips of Current employer
    Copy of all educational certificates (SSLC, PUC, Graduation, Post Graduation, semester wise),
    ID proof: Aadhar card, PAN card
    One passport size photo

    Venue : 
    Hikal Limited Unit 2,
    28, KIADB Indl. Area, 
    Jigani,Anekal Taluk,
    Bangalore - 560105
    (landmark : APC Circle)
    Phone :+ Direct :- #91 08110421094
     
    shikha_saxena@hikal.com

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