Cipla B Pharma QA Job Opening 2022 – Candidates Apply Online
Cipla Hiring Junior Team Member – QA. B Pharma job opening 2022. Pharma job opening 2022. Pharmacy job opening 2022, Pharma job vacancy 2022, Pharma job 2022. Candidates with a bachelor’s degree in pharma may apply for the job vacancy at Cipla Ltd. Interested and eligible candidates may check out all the details on the same below:
Job Title: Junior Team Member – QA (65934)
Division Quality
Department Quality
Employment Type Permanent
Education Qualification B. Pharma/ M.Sc
Relevant Work Experience 2 years of experience in quality assurance department
Competencies/Skills
- 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.)
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 mannerII. 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 certificates, dossiers (TDP & RAP), and development report at unit for the execution of new products smoothly
VI. Coordinate with auditors and site teams for regulatory and customer inspection/ audit at the site to meet the regulatory expectation and acquire GMP approvals
VII. Prepare the final draft of compliance to audit observation and check whether it is in line with cGMP requirements 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
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