Officer / Sr. Officer in IPQA – QA in Pharma MNC at Ahmedabad

Job Description
  • To verify raw material, primary packing material at the time of material issuance and material dispensing against Technical Package / Standard Material Requirement Form and approve the process step.
  • To perform routine IPQA monitoring like volume check, critical control step verification during manufacturing of the product, sampling and periodic verification activities and if any deviation / abnormal observation in terms of noncompliance to Good Manufacturing Practice (GMP) observed, bring to the notice of Executive (Shift in charge).
  • To get issued Soft copy from Corporate Quality Assurance (CQA) Department and prepare & review MBD and MPD.
  • To convert approved MBD / MPD into of Batch Manufacturing Record (BMR) and Batch Packing Record (BPR) and then in the pdf format.
  • To Submit soft copy of MBD / MPD to CQA.
  • To verify sample / good destruction process and report any gap to Department Head and take corrective and preventive action in coordination with respective Department Head.
  • To raise request for stability batch destruction after expiry period is over.
  • Receipt and handling of data loggers. Place data loggers in consignment at the time of shipment.
  • To carry out reconciliation and physical verification of the returned goods.
  • To verify headspace oxygen and dissolve oxygen during in process monitoring.
  • To verify logbooks, online documents, records, analysis report and other supporting documents related to products manufactured in the plant.

Industry:Pharma / Biotech / Clinical Research

Functional Area:Other

Role:Other

Keyskills

QA, IPQA

Education-

UG:Any Graduate – Any Specialization, B.PharmaPharmacy

PG:MS/M.Sc(Science) – Any Specialization, Chemistry, Microbiology