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Troikaa Pharmaceuticals

Officer - QC - V'Nagar

Ahmedabad · Staff/Principal

Good timing - competition is buildingVerified listingPosted 3d ago

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

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86Overall
64Skills
97Experience

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What we know about this role

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First 72 hours

Window passed - posted 3d ago

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Skills required

3 listed
Standard Operating ProcedureInstrument CalibrationSample Preparation
Standard Operating ProcedureInstrument CalibrationSample Preparation

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Job description

To perform accurate and reliable analysis of Raw Material as per method of analysis or protocol.

To perform method transfer, method verification, analytical method validation and protocol base study.

To record the procedure of the test performed and observations contemporaneously.

To review the results against specification / acceptance criteria mentioned in the protocol. If any abnormality to be informed immediately to Section head.

To review the Method of analysis / worksheet prior to analysis and shall inform to the section In charge for the potential failure (if any).

Preparation of Standard Test Procedure, Method of Analysis, Specification and Standard Operating Procedure as and when required

To operate the QC equipment(s).

Sample Receive:

To receive the sample along with Test request slip (TRF) or Goods Receipt Notes (GRN). To verify the physical sample condition and sample label against TRF / GRN.

To allocate the AR. No. in ‘Inward register’.

General :

To verify the sample details (Material Name, Sample Name, Batch No.,etc.) before perform the analysis.

To ensure the current version method of analysis and specification available before analysis.

To verify the instrument calibration status before perform the analysis.

At start of the shift inform to operator/ supervisor for requirement of chemical usage in analysis.

After completion of analysis enter the results in LIMS software.

Record the analytical document on line (contemporaneously) and submit to reviewer / section head after completion

To follow good laboratory practices.

Reporting of all above analytical work to section head / In-charge-QC.

Sample preparation & Related documentation for the sample to be sent to the outside laboratory

To participate in investigations of OOS / laboratory incident / OOT / deviation.

To inform the section In charge for the break-down of equipment.

Immediately information to the In-charge-QC in case of any abnormal observation found during analysis.

Any data integrity related observation in the department shall be bring to notice of QC-Head

To maintain the discipline in laboratory.

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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

Daily job drops, skill trends and free resources - posted straight to the group. Leave any time.

Join WhatsAppJoin Telegram

No spam. Just jobs and resources.

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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