Ahmedabad · Staff/Principal
Applicants who checked fit first are 3.1× more likely to hear back
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
HIGH
Our tracked job listings for Troikaa Pharmaceuticals show strong recent activity.
First 72 hours
Window passed - posted 3d agoEarly applicants get seen before the pile builds.
Not a repost
The first time we've seen this listing - it hasn't been closed and reopened.
You almost certainly match several of these already. Unlock your skill map to see the matches, the gaps, and what to fix first.
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. |
Your match score, skill map and tracker stay free.
Skip jobs with hidden dealbreakers. See what they actually need, what's easy to miss, and how they describe the team.
Ground Reality on every job, plus Insider Path, practice interviews and resume tailoring.
We help you find people there who worked or studied where you did, and draft your first message and follow-up.
Free · no signup
Daily job drops, skill trends and free resources - posted straight to the group. Leave any time.
No spam. Just jobs and resources.
Why people use ASAI
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.
More Security Engineer roles in Ahmedabad
See allKeep browsing