Zydus Lifesciences Limited, After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times. Our legacy of over 70 years in healthcare and being dedicated to life in all its dimensions is reaffirmed in our new mission, vision and purpose. Unifying ourselves under the Zydus name, Cadila Healthcare Ltd., is renamed as Zydus Lifesciences Ltd.
Vacancy details:
- Department: Trainee Officer /Officer -Continous Process Verification (statistics) - CPV
- Qualification: MSc Statistics / Bio Statistics / Applied Statistics
- Experience: Between 0-2 Years Of Experience
- Salary:₹ Not Disclosed by Recruiter
Job Description: Greeting From Cipla Pharmaceutical Ltd.!!!!!
Important Details :
- Job Location: Ahemdbaad , Baddi , Goa , Sikkim , Daman
- Post of date:02/02/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
Inviting candidates for a walk-in interview for the CPV department for Manufacturing plants across India.
To apply, visit https://bit.ly/48VvRcv
JOB RESPONSIBILITY :
1. Statistical interpretation and graphical presentation for Product Quality Review and trending the data for continued process verification.
2. To perform and review capability analysis as a part of PQR.
3. To perform and review regression analysis for estimation of the product shelf life.
4. Trending analysis, implementation & Application of SPC Charts for processing and analytical parameters as a part of CPV and PQR.
5. Application of various statistical techniques to characterize and reduce process variability and optimize performance.
6. To perform various parametric & non parametric statistical tests: t-test, ANOVA, ANCOVA, Chi-square, F-test, Sign test etc.
7. To derive conclusion & interpretation of statistical results for PQR.
8.To prepare and review Product Quality Review and continued process verification report.
9. Handling of different software like Trackwise and SAP for data collection. 10. Establishing control limit against the established specification limit for analytical parameters.
11.To provide the training to belonging personnel for the Statistical trending and interpretation.
12. To review the batch manufacturing records and batch packing records. 13. Leading QMS activities viz continued process verification (Manufacturing as well as Packing related CPV), Annual Product Review Report and Change Control.
14. Ensuring implementation of identified CAPA (Corrective actions & Preventive actions).
15. Reviewing trend analysis of Critical Process Parameters and Critical Quality Attributes of the finished product as well as stability batch using MINITAB for identification of early alarm in process of dosage forms.
16. Escalating senior management about project process and critical issues that can impact the quality product through regular reports.
17. Maintain all quality related communication, documents and records.
18. Preparation and reviewing of SOPs ( Standard Operating Procedure).
19. Provide the training for 21st Century Quality Basics ( Basic and advance statistics) for CFT.
20. Multipal statistical tools use in APQR and CPV preparation i.e. Statistical process control (SPC), Normality, Process Capability, Process Performance, ANOVA, Regression Analysis, Control Chart, Perato Chart, Distribution Chart (Box plot), shelf life estimation (ANCOVA) by using Minitab Software.
21. Trending the batch manufacturing records, batch packing records and review and timely escalation.
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