Officer QA IPQA-Thol
Ahmedabad · Mid Level
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What we know about this role
HIGH
Our tracked job listings for Troikaa Pharmaceuticals show strong recent activity.
First 72 hours
Window passed - posted 7d 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.
Skills required
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Job description
Sr. No. | Responsibilities |
1.0 | Line Clearance activity. |
1.1 | Line clearance of area and Equipments as per checklists of SOP at various stages of dispensing, manufacturing and packing activity. |
2.0 | In Process activity. |
2.1 | Approval of Specimens, In Process control as per mentioned in SOP and batch records at various stages of all dosage forms. |
3.0 | Monitoring of cGMP practices at shop floor. |
4.0 | Sampling Activity. |
4.1 | Sampling of in process bulk product, finished product, PV, CV samples, Wash water, Retain samples as per SOP/ protocol and registration sample as per RA request. |
5.0 | Verification of status labels on equipments and containers. |
6.0 | Verification of Documents. |
6.1 | Review of temperature, relative humidity and differential pressure records, Operational and Cleaning records and related documents. |
7.0 | Disposition of Raw material, Packing material, in process/ semi-finished and finished products. |
8.0 | Handling of raw material and packing material dispensing activity. |
9.0 | Handling of QMS related activities. |
9.1 | Initiation of Change Control Form, Deviation. |
10.0 | Review of Documents. |
10.1 | Review of batch manufacturing and batch packing records during batch processing and after completion of batch processing. |
10.2 | Review of Logbooks. |
11.0 | Annual Product Quality Review. |
11.1 | Collection of Data for APQR, Preparation of APQR. |
12.0 | Handling of Documents. |
12.1 | Numbering and Evaluation of Code to code, Plant to Plant, Wrong Punching, Transfer Posting, Breakdown Memo, Predictive Maintenance Format. |
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