Cipla Limited, we constantly work towards ensuring access to high quality and affordable medicines to support patients in need. Which is why, we have been trusted by health care professionals and patients across geographies for the last 8 decades. In India, Cipla Ltd has its manufacturing presence at Bangalore (Bommasandra & Virgonagar), Indore, Goa, Baddi, Kurkumbh (Near Pune), Patalganga (Near Mumbai) & Sikkim.
Walk-in drive for Apprentice hiring in Quality Control
- JOB ROLE: Apprentice
- DEPARTMENT: Quality Control
- DESIGNATION: Apprentice
- QUALIFICATION: MSc. (Analytical Chemistry) 2023 Pass-out with First Class
JOB DESCRIPTION:
- Ensure Good Laboratory Practices
- Daily Balance & PH Calibration
- Testing of Raw materials
- Upkeep of analytical reference registers
WALK-IN INTERVIEW DETAILS:
- DATE: 9th NOVEMBER 2023
- TIME: 10:00 AM – 4:00 PM
- Reporting Time:9:30 AM
- VENUE: Cipla Ltd, D-22 (Unit-III) MIDC Kurkumbh, Tal Daund Dist: Pune – 413 802
LINK TO APPLY:
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Scan the QR code
IMPORTANT NOTE:
- Please register using QR code before reaching the venue
- Please carry your smartphones to the venue
Responsibilities:1. To ensure compliance with current good laboratory practices as laid down in the quality control procedures.
2. Maintain and upkeep of laboratory working area.
3. Analysis of Raw materials (API and excipients), finished Products, in-process samples and Stability Samples. 4.During testing of samples the following should be ensured.
- Should review intimation documents for details and confirm the same is matching with the details of the sample and specification provided for the analysis.
- Should read the relevant specification and organize the work in such a manner that testing can be completed in stipulated time.
- Should be aware of potential problems that could occur during the testing process and should watch for steps that could create inaccurate results.
- Should ensure use of instruments / equipment’s meeting established performance.
- Specification and are properly calibrated.
- Should ensure use of valid reagents, chemicals, standards, appropriate clean and dry glassware etc. for analysis. ensure use of valid reagents
- Should follow correct analytical techniques during preparation of solutions like Weighing, pipetting, dilutions, sonication, filtration etc.
Responsibilities:
4. During testing of samples the following should be ensured. (Cont…)
- Should follow the specific instruction / precautions provided based on material/ product characteristics in the respective specification.
- Should perform testing of samples as per procedure specified in specification and make concomitant entries in test data sheet.
- Should set parameters of instrument as given in specification and should ensure compliance of system suitability parameters before commencing for sample analysis.
- Should follow GLP for documentation.
- Should ensure that the figures for quantitative tests are rounded to the number of decimals indicated in the standards of specification.
- Should avoid transcription error during data entry and should ensure use of validated software for calculations.
- Should check result for test performed for compliance with the standards specified in specifications and should not discard test preparations or standard preparations before the data are reviewed and verified
- Prompt reporting of non-conformances such as OOS, OOT, laboratory errors, instrument malfunctioning etc or obvious error occurred during preparation to Section Head.
- Should ensure completeness of entries of all the tests performed and compilation of relevant data before submission for review.
5. Initiation and completion of work output report.
6. Receipt of requirement for method validation.
7. If method validation is already available, comparison of the same with current method.
8. Documenting the details in Validation / verification evaluation checklist.
9. Selection of validation / verification parameters as per SOP 1035-L-0016.
10. Preparation of method validation / verification protocol, experimental design and TDS.
11. Performing method validation analysis and reporting of the results.
12. Submitting intimation to respective department along with required documents if any.
13. Involvement in the investigation of non-conformances such as OOS, OOT, Incidences etc. 14. Disposal of balance samples after completion of analysis and review.
15. Involvement in the impact evaluation of instrument breakdown or calibration failures on Previously released sample.
16. Analysis of materials for qualification as laboratory standards against reference/ certified standards.
17. Following the laid down safety precautions while working in the laboratory.
18. Analysis for personal validation and analytical method transfer.
19. Upkeep of Analytical Reference registers and allocation of A. R. No.
20. Upkeep of completed reports.
21. Daily balance and pH meter calibration.
22. Daily temperature & humidity recording & maintain the laboratory cleaning record, in absence of non-routine support analyst.
23. Handling of LIMS related activities,
24. Work as certified instructor.
25. Calibration and Maintenance of Instrument and Equipment as per Schedule.
26. G of software as per SOP 1035-G-0039.
27. Daily Standardization of KF Reagents, Analysis of water content & LOD, ROI, Solubility, Limit Test, tapped density, Sieve Test etc.
28. Ensure reliability of data, either paper or electronic, with an intention to integrity of GXP data is included. 29. Any non-conformance identified should be reported to the reporting manager / designee & to be addressed through appropriate QMS procedures.
30. To operate the systems like LIMS, CipDox, LMS, and Tiamo software etc. and Other Quality Control Software based on the roles and rights / Privileges provided in the application.
31. Procurement of chemicals, accessories and upkeep of the same.
32. Any other assignment allocated by section head/ Head unit quality Control.
