Cipla Job opening for Junior Team Member – QA – apply Now

Cipla Limited, a global pharmaceutical leader, stands as a beacon of innovation and quality in the healthcare industry

Cipla Job opening for Junior Team Member – QA – apply Now

Cipla Job opening for Junior Team Member – QA – apply Now

About the job

Division

Quality

Department

Quality

Employment Type

Permanent

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

Education Qualification

B. Pharma/ M.Sc

Relevant Work Experience

2 years of experience in quality assurance department

Competencies/Skills

Collaborate to Succeed

Innovate to Excel

Perform with Accountability

Lead with Empathy

Act with Agility

Strong Domain Knowledge

People Management

Job Location

Goa

Shift Hours

APPLY HERE

https://chat.whatsapp.com/DO9PMPj2H3K4SikyHri52x

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This Post Has One Comment

  1. Hemanth

    I have 10 months experience in ipqa packing and I am currently working in laurus labs unit 2 atchuthapuram (vizag) please give me a chance to join your organisation if there is any possibility which is help my career growth and help the organisation too please give me a chance to proov me

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