Join Cipla Ltd Goa as a Junior Team Member QA – B. Pharma/ M. Sc can Apply

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Take the first step towards a fulfilling career in pharmaceutical production with Cipla Ltd! We’re on the lookout for driven B. Pharma/ M. Sc graduates to join us as Junior Team Members in Quality Assurance. This is your opportunity to be part of a renowned company in Goa, where you’ll contribute to the manufacturing of life-saving medications. Don’t miss out on this chance to kickstart your journey in the pharmaceutical industry with a trusted leader dedicated to excellence and innovation.

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Job Purpose

Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines.

Accountabilities

I. Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
II. Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
III. Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
IV. Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
V. Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
VI. Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
VII. Prepare final draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements
VIII. Collect, compile and review raw data and finalise the same for timely submission of MHRA, UK interim update document to corporate as per agency requirement by tracking interim updates at a site level, for risk based inspection planning
IX. Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP
X. Execute on time and errorless submissions by reviewing product license, all certificates for product registration and tender , staff approvals and other applications to adhere to legal requirements
XI. Support in CDSCO and state FDA inspection to be GMP compliant and getting product licence, FDA stall approvals by ensuring cross functional interaction

Competencies/Skills

1. Collaborate to Succeed
2. Innovate to Excel
3. Perform with Accountability
4. Lead with Empathy
5. Act with Agility
6. Strong Domain Knowledge
7. People Management

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