Cipla Hiring Junior Team Member – QA – B Pharma/ MSc

Cipla Hiring Junior Team Member – QA

Are you a B Pharma or MSc graduate with experience in Quality Assurance? Cipla, one of the leading pharmaceutical companies, is looking for a Junior Team Member in QA to join their team in Rangpo, Sikkim. This is a fantastic opportunity to work in a dynamic environment and advance your career in the pharma industry.

Job Overview

Position: Junior Team Member – Quality Assurance (QA)
Location: Rangpo, Sikkim, India
Division: Quality
Department: Quality
Employment Type: Permanent
Req ID: 85805

Job Purpose

The primary goal of the Junior Team Member – QA role is to ensure compliance with company quality policies and applicable regulatory guidelines. The role involves reviewing site compliance for deficiency responses, preparing master validation protocols, and supporting regulatory inspections.

Responsibilities

• Collate, review and provide required work plans on received deficiencies to HO in order to respond to regulatory authorities in a timely manner
• Review Master Validation protocol and report for timely execution of validation batches and timely submission of documents in order to response for deficiencies
• Review annual product quality review report at units for completeness and data correctness to ensure compliance to cGMP requirements and audit readiness
• Review, upkeep and issue regulated market technical agreements at site for execution of batches as per customer requirement
• Receive and distribute approval certificate, dossiers (TDP & RAP) and development report at unit for execution of new products smoothly
• Coordinate with auditors and site teams for regulatory and customer inspection/ audit at site to meet regulatory expectation and acquire GMP approvals
• 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
• 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
• Drive continuous improvement initiatives in CQA to facilitate adherence to cGMP
• 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
• Support in CDSCO and state FDA inspection to be GMP compliant and getting product licence, FDA stall approvals by ensuring cross functional interaction

Qualifications

• Education: B Pharma or MSc degree.
• Experience: At least 2 years of experience in the quality assurance department.
• Skills:
  • Strong domain knowledge
  • Excellent organizational and analytical skills
  • Effective communication and collaboration abilities
  • Ability to innovate and excel in tasks
  • People management and leadership qualities

How to Apply

If you meet the qualifications and are excited about this opportunity, apply now to join Cipla’s dynamic team. Submit your application through the Cipla Career Page.