Sobre esta vaga de Senior Executive - QA na Piramal Pharma
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Division
Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.
This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.
Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.
For more details, please visit : www.piramalpharmasolutions.com
Job Title
Senior Executive - QAJob Description
Personnel with Analytical QA background. Review analytical raw data, electronic data, and audit trails for laboratory instruments. Ensure laboratory compliance with GMP/GxP requirements and established procedures. Investigate and manage QMS events- including OOS, OOT, OOE, deviations, and incidents. Review, approve, and maintain analytical SOPs and quality documents for continual improvement.To carry out activities of Analytical QA personnel.
Review of analytical raw data and documents.
Review of electronic data and audit trail for instruments like HPLC, GC-MS, ICPMS, LC-MS, XRPD.
Monitoring compliance in laboratory as per laid down procedures.
Investigation of QMS – OOS, Deviation, Incident, OOT, OOE.
Review of Analytical SOPs for compliance requirements and continual improvement
Review and approval of analytical documents such as specifications, test procedures, analytical method validation / verification protocols & reports, Analytical method transfer protocols & reports, stability reports, investigation reports, trend reports etc.
Review and approve the raw material, packing material, finished product analytical data.
Review of Product development reports.
Review of computer system validation documents.
Prepare SOPs related to QA Department.
Periodic review of analytical records (instrument logbooks, calibration records, standard management records etc.)
Impart induction training on topics and on which training has been taken.
Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same.