Cipla Released Job Openings On 04/02/2022.Cipla Limited is an Indian multinational pharmaceutical company, headquartered in Mumbai, India.Interested and eligible candidates required to fill application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Team Member – QMS & Compliance as follows.
Vacancy Details:
Cipla Recruiting B. Sc,M. Sc,B. Pharma candidates with 3-5 years of Experience for Team Member – QMS & Compliance Position.Complete Details for the Team Member – QMS & Compliance as follows.
Important Details :
- Location: Sikkim
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application:04/02/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
Coordinate for audits and track the compliance of non-conformances, ensure implementation of QMS system, review all master documents and APQR data and perform timely release of batches manufactured at CMO/PTL sites to deliver quality products and meet regulatory compliance
Accountabilities
I. Review batch release documents of CMO/PTL sites to ensure the quality product is released in market to meet the regulatory requirements and patient safety
II. Evaluate logged deviation and change control for investigation and CAPA implementation in order to ensure no recurrence of the deviation
III. Initiation and track the batch failure investigation, product recall and Implementation of CAPA to avoid reoccurrence of batch failure and recall
IV. Identify exact root cause for market complaints and ensure implementation of CAPA in order to avoid reoccurrence of complaint in future and no impact on patient safety and compliance of regulatory requirements
V. Plan, execute audits of CMO/PTL sites to ensure manufacturing unit can produce quality products and PTL meets the testing requirements
VI. Plan and execute risk management programme for CMO/PTL sites to identify, prioritize and mitigate quality risks
VII. Review master batch documents to ensure it contains all the required instructions to manufacture quality product meeting customer and regulatory requirement
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