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Associate - VI training

2.00 to 3.00 Years   Chennai   26 May, 2021
Job LocationChennai
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

  • Understanding of pharmaceutical manufacturing, packaging, quality assurance.
  • Understanding of visual inspection operation.
  • Good interpersonal skills.
  • Good people management skills.
  • Preparation of modules expertise.
  • Assist training manager in daily operations as needed.
  • Impart training and qualification to Manual Visual inspectors (Upstream and Downstream production inspectors, AQL inspectors, Retention sample inspectors) for manual visual inspection of Clear Glass Vials, Plastic Vials, Clear Glass Ampoules, Amber Glass Vials and Propofol filled commodities.
  • Impart training and qualification to inspector trainees from downstream production for Semi-automatic visual inspection of Clear Glass Vials, Plastic Vials, Clear Glass Ampoules, Amber Glass Vials and Propofol filled commodities.
  • Impart training and qualification to in-coming inspectors on Tubular Glass Vials, Molded Glass Vials, Ampoules and Plastic Vials.
  • Scheduling of re-qualifications and initial qualifications for manual and semi-automatic visual inspectors as per requirement from production (Upstream, Downstream), MQA, QC-Packing and retention sample area.
  • Making PLS entries of qualified inspectors to track their re-qualification due dates.
  • Archival of visual inspector qualification documents.
  • Preparation and approval of list of qualified inspectors for manual and semi-automatic visual inspection.
  • Coordinate with OHC for scheduling annual eye checkup for timely completion to avoid over dues.
  • Evaluation of new defect/atypical defect by coordinating with Site expert panel and taking concurrence by referring PDA and USP guidance documents.
  • Supporting production and AQL inspectors if there is any uncertainty regarding identification of defects and its classification during visual inspection of commercial batches.
  • Impart new defect/atypical defect training to qualified visual inspectors.
  • Preparation, labelling and maintenance of defect kits used for Automatic, Semi-automatic and Manual visual inspection.
  • Re-inspection, tracking of expiry dates and destruction of defect kits used for manual and semi-automatic visual inspection.
  • Co-ordinate with Rocky Mount site for procurement of defect kits.
  • Initiation of change controls and it s routing for approval followed by closure.
  • Coordinate for effective closure of CAPAs, Knapp study protocols and defect kits protocols.
  • Logbooks indent, issuance, review and submission for archival.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Manufacturing #LI-PFE,

Keyskills :
daily operationspeople managementvisual inspectionposition managementlegislative relationspharmaceutical manufacturing

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