Hurry! Apply Online for Cipla BPharma QA Recruitment in Goa

Cipla BPharma QA Recruitment – Apply Online

Welcome to Cipla! We are a leading pharmaceutical company committed to providing high-quality medicines to people around the world. Our mission is to make healthcare accessible to everyone, and we are proud to play a crucial role in improving people’s lives.

Job Title: Team Member – QA

Requisition ID: 80510

Division: Quality

Department: Quality

Employment Type: Permanent

Job Purpose:

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

Accountabilities:

1. Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
2. Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
3. Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
4. Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
5. Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
6. Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
7. Prepare the final draft of compliance to audit observation and check whether it is in line with cGMP requirement to avoid regulatory action and continual improvements
8. Collect, compile and review raw data and finalize 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
9. Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP
10. 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
11. Support in CDSCO and state FDA inspection to be GMP compliant and getting product license, FDA stall approvals by ensuring cross-functional interaction

Education Qualification:

B. Pharma/ M.Sc

Relevant Work Experience:

3-4 years of experience in the quality assurance department

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

Job Location: Goa

Apply Now:

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