Cipla Ltd Recruitment 2023. Cipla Ltd Notification full details below.Intrested and eligible candidates can Send Apply Online.Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the same purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms.
- Vacancy details:
- Post Name: Team Member – Quality Compliance
- Qualification: B. Sc. / M. Sc. / B. Pharma
- Experienced:5 years of experience in quality assurance
Job Description: Greeting From Cipla Ltd !!!!
- Important Details :
- Location: India -Goa
- Post of date:19/01/2023
- Selection Process: The selection will be on the basis of Interview.
Roles and Responsibilities:
Division
Department
Employment Type
Job Purpose
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.
Education Qualification
B. Sc. / M. Sc. / B. Pharma
Relevant Work Experience
5 years of experience in quality assurance
Competencies/Skills
Job Location
Goa
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