Cipla Ltd Walk-in Interview 2022 B. Pharma/ M.Sc for Team Member – QA At India – Sikkim – Rangpo. Cipla Ltd Notification full details below.Interested and eligible candidates send Your Resume.
- Vacancy details:
- Post Name: Team Member – QA
- Qualification: B. Pharma/ M.Sc
- Experienced:3 to 4 years
Job Description: Cipla Ltd Hiring For Team Member – QA ! Communication Skills (clarity of thought, comprehension) Likely potential for growth Job / Product / Technical Knowledge / Pharma domain knowledge Presentation & Interpersonal skills (If applicable) Managerial or People Management skills Safety awareness (If applicable)
- Important Details :
- Location: India – Sikkim – Rangpo
- Post of date:14/03/2022
- Selection Process: The selection will be on the basis of Interview.
- How to Apply :
Step 1: Click on below link and you will be redirected to Career Page of Recruiting Company or Career portal.
Step 2. Register on Career Page of the Company or Career Portal by giving log in credentials and other personal or education details .
Step 3.Upon successful registration .User need to log in with credentials.
Step 4.Once logged in, User need to fill the all relevant personal ,educational , Work experience details ,attach resume and submit application form.
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