Pearldrops Healthcare Staffing
2d ago
  • Reporting Relationship; Head,Quality Control;
  • Microbiology Section - Planning and work allocation for. Micro activity, if required
  • Ensuring the quality and integrity of all GxP data and documentation generated.
  • Monitoring of sampling activity of incoming Raw materials, Packing materials & Microbiological samples.
  • Microbiological testing & monitoring of Finish goods, Raw materials, packing materials, Water samples & environments.
  • Ensure fully Engagement and Involvement regarding awareness, clarity maintained related to data integrity.
  • Knowledge of EHS Demonstrates basic knowledge of environment, Health and safety requirements within work area in order to comply to all set standard, identify and escalate potential hazards.
  • Investigation Skills Demonstrates expert knowledge of investigation procedures and tools, domain knowledge, impact assessment and implications on related areas in order to have comprehensive investigation to avoid repeat of issues / incidents, review trends and understand issues impacting organization and design CAPA.
  • Calibration of Equipments / Instruments as per the planner.
  • To follow & maintain the practices of cGMP & GLP in QC Dept.
  • Co-ordination with Internal & External customers.
  • All quality control related documents, records, raw data shall be reviewed.
  • Review the documentation of Deviations, change controls, Out of specifications if any.
  • Execution of Analytical Method Validation of Microbial tests.
  • Trending & review of microbial analytical data
  • Investigation of OOS, deviation of Raw, packaging and finished material analysis.
  • Imparting the Internal training activities for Quality control personals.
  • Monitoring the calibration / validation planner for Instruments / Equipment.
  • The procurement of Microbial cultures, medias, reference standards from authorized supplier and laboratory chemicals
  • To prepare and update the Testing procedures and Specifications and related documents.
  • Destruction of respective records & QC Samples like Retention samples of Raw Materials, analyzed samples.
  • To comply Internal and External Audit Observations.
  • Issuance of QC analytical data sheets
  • Evaluation, validation and monitoring of critical control points with respect to process as part of cGLP / GMP requirements.
  • Preparation and destruction of Medias.
  • Preparation of Microbial inoculum and growth promotion test.
  • Preparation & maintenance of sub cultures.


    Person Specification :

  • Qualification : M.Sc (Microbiology)
  • Total Experience : 5 to 7 Years
  • Apply
    My Email
    By clicking on "Continue", I give neuvoo consent to process my data and to send me email alerts, as detailed in neuvoo's Privacy Policy . I may withdraw my consent or unsubscribe at any time.
    Application form