Job Description
Vacancy for Junior Team Member QA at Cipla 2023. Review the compliance level of site for deficiency response, prepare master validation protocol and report as per company quality policy and applicable regulatory guidelines.
| Organization | Cipla |
| Post Name | Junior Team Member – QA |
| Job Location | Sikkim – Rangpo |
| Official Website | https://www.cipla.com/home |
Job Title/Position:
Junior Team Member – QA
Job Overview:
Job vacancy for Pharmacy, Science
Job Location:
Sikkim – Rangpo
 |
 |
What are the Key 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
What are the Educational Qualification(s) for this position(s)?
B. Pharma/ M.Sc
What is the Experience Required for this Job?
2 years of experience in quality assurance department – IPQA
What are the Preferred Skills required for this Job/Position?
- 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)
- Relevance of Previous Experience
- Comprehension, Analytical & Problem solving abilities
- Productivity & Result Orientation (If applicable)
- Attitude
- Qualification fitment
- Sales drive (If applicable)
- Personality traits (Individualistic / Team player, Out spoken, Maturity level etc.)
Related:
- Vacancy for Project Associate at IMTech 2023
- National Post Doctoral Fellowship (N-PDF) at SERB 2023
- Admission to THSTI-Manipal PhD Program 2023-24 (Monsoon Session)
- Trainee at Kerala State Drugs & Pharmaceuticals Ltd
- RCB-NABI Ph.D. (Biotechnology) Program Admission 2023
Detailed notice
You can check Labmonk scholarship for scholarship information.
Check out and answer Labmonk’s daily quiz.
You can read other career related articles on Labmonk Blog. Search Labmonk Blog on google and click the first link for more articles.
