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Troikaa Pharmaceuticals

Sr Officer - IPQA - Thol - 3719

Ahmedabad · Senior

Older listing - lower visibility likelyVerified listingPosted 587d ago

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86Overall
64Skills
97Experience

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Window passed - posted 587d ago

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Skills required

9 listed
Quality ControlPreventive MaintenanceSample CollectionChange ControlProcess ValidationTime StudyCalibrationSampling (Statistics)+1 more
Quality ControlPreventive MaintenanceSample CollectionChange ControlProcess Validation

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Job description

  • Handling of overall IPQA activities
  • LINE CLEARANCE & IN-PROCESS ACTIVITY:
  • Line clearance in Injectable manufacturing, packing & warehouse dept.
  • To verified the documents of area cleaning, equipment cleaning and others.
  • Verification of temperature & relative humidity record and other logbooks of Injectable block.
  • In-Process quality control parameters check during various stages of manufacturing, filling & packing dept. Verification of Preventive Maintenance of Equipment's.
  • Handling & Review of Breakdown documents of equipment's.
  • Calibration & Verification of weighing balance.
  • Additional material verification of raw material & packing material.
  • Wash water and Swab sample collection at different stages of manufacturing and filling.
  • Verification of cleaned containers and utensils with respective logbook and checklist.
  • Sampling Activity:
  • Sampling of In-process samples, Bulk samples, Finished samples and Validation samples of Injectable area.
  • Sampling and Handling of Stability sample, Reference sample and Registration sample.
  • DOCUMENTATION:
  • Preparation of new SOPS and GMP documents, revision of SOPs and preparation of Training documents as and when required.
  • Initiation of Change control, Deviation and CAPA and assist Department In-charge in Failure investigation and Root cause analysis.
  • Handling & online filling of all GMP documents.
  • Review of the batch manufacturing & batch packing record at every stage of operation.
  • Verification of Material requisition slip and Dispensing slip at Manufacturing & Packing stage.
  • CROSS FUNCTIONAL ACTIVITY:
  • Verification & Execution of Process validation Study and Hold Time Study protocols.
  • Additional responsibilities given by Head of the department
  • To carryout SAP related activities.

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Two ways in

Applicants who checked fit first are 3.1× more likely to hear back

Your match scoreFree · sign in
86Overall
64Skills
97Experience

Your score for this role already exists

ASAI compared this JD against 41 signals - skills, seniority, domain, stack overlap etc. Add a resume and it unlocks in about 30 seconds.

Always free · no credit card · 1 tap with Google

Free · no signup

Get tomorrow's jobs before you have to search

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Why people use ASAI

Someone shared one job with you. ASAI keeps finding the rest.

  • Scored, not searched. Every role ranked against your actual profile.

  • Alerts as often as hourly. Reach new roles while the pile is still small.

  • Skill gaps, spelled out. See exactly which requirements you don't meet yet.

  • Verified jobs, only. Say no to ghost jobs. Your time deserves respect.

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