Senior Executive
4 days ago
Job Description:
To Provide Statistical Support through preparation/review of statistical reports to all Cipla Global manufacturing sites.
Assist unit APQR personnel to prepare Statistical analysis and graphs/trend in APQR reports for the respective site.
Implement new statistical concepts whenever required to overcome departures during validation batches of the products.
To involve and provide statistical Justification for deviations /OOTs /OOS reports.
Providing trainings internally on Basic Pharmaceutical Statistics, Statistical Process Monitoring, Shelf-life analysis to APQR/CPV team and Validation teams with live examples.
Creating and developing tools and process through data visualization/reporting/analytics dashboard to improve quality and productivity within statistics function.
Implementing new Statistical concepts in APQR and CPV SOPs in CIPLA, which help to monitor the worst-case product statistically by applying advanced statistical tools (in line with regulatory expectations) .
Educational qualifications:
M.Sc., in Statistics/Masters in Chemical Eng. with Data Science/Analytics or Other relevant post graduate degree with desired experience.
Relevant experience:
M.Sc., in Statistics/masters in chemical Eng./Data Science/Analytics or Other relevant post graduate degree with minimum 2-3 Years of Experience in application of statistical/data science/analytics tools in pharmaceutical industry especially in pharma manufacturing and development, desirable to have pharmaceutical industry experience.
SPC/SQC, Data Science, Analytics Visual Dashboards creation, Lean Six Sigma, Good Communication Skills, well versed with data analysis and statistical applications, troubleshooting during Pharma Manufacturing process.
Software applications required: MINITAB (experience compulsory), JMP, MS office, MS SharePoint, Power BI and Python/R (any one desirable) or any other Statistical software.
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