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Teva Quality Control Technician II 
India, Madhya Pradesh, Gwalior 
128369218

30.06.2024
How you’ll spend your day
  • 24 × 7 audit readiness.

  • Participation in internal, external, regulatory audits.

  • Ensure 100% participation in training’s against CAPA’s.

  • Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge.

  • Supporting to share required documents from QC to RA/ other requirement.

  • Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader /Manger.

  • Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory.

  • Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms.

JD Contd...
  • Perform analytical test according to the monograph and SOP.

  • Responsible for calibration and verification of instruments.

  • Maintaining of reserved samples room and chambers / autoclaves / incubators.

  • Help to in charge in preparation of documents related to department (like STP’s, SOP’s and etc.)

  • Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis.

  • Must be ensured sampled, approved and rejected labels timely as required.

  • Responsible to maintain the stock record of chemicals and reconciliation of standards.

  • Any other job assigned by the Manger -QC Manger or group leader-QC

Your experience and qualifications

Bachelor/Master of science (Chemistry) or B-Pharm

3-5years of experience

Reports To

Quality Control Analyst II