Novartis Walk-in Interview 2022 B. Pharm/M. Pharm/M.Sc. from reputed institute for Sr. Executive Quality Assurance At Navi Mumbai . Novartis Notification full detailed below..Interested and eligible candidates can Apply Now.
- Vacancy details:
- Post Name: Sr. Executive Quality Assurance
- Qualification: B. Pharm/M. Pharm/M.Sc. from reputed institute
- Experienced:05 to 10 years
Job Description: Novartis Hiring For Sr. Executive Quality Assurance !
- Important Details :
- Location:Navi Mumbai
- Post of date:08/03/2022
- Selection Process: The selection will be on the basis of Interview.
Your key responsibilities:
Your responsibilities include, but are not limited to:
• Review of Equipment / System Qualification document (URS, DQ, IQ, OPQ etc.)
• Preparation, distribution, and monitoring of annual schedule for periodic review for need of re-qualification of equipment / system to all user departments.
• To archive and maintain qualification documents. Preparation. Review and / or approval of Failure Mode Effective Analysis (FMEA) & Quality Risk Assessment.
• Periodic overview of engineering & Admin Logbooks. Review and/ or approval of transport rout qualification document (SOP, transport qualification protocols and transport qualification reports)
• Review of calibration and preventive maintenance activities of manufacturing equipment. Review / Approve of SOP and Documents related to equipment / system qualification.
• QA oversight of engineering department, utility, service floor, calibration, and maintenance activities etc.
• To review / approve periodic review reports for need of re-qualification of equipment / system.
• Review and / or approval of track and trace project documents. To perform periodic user management of standalone and network system as an Administrator for laboratory instrument.
Minimum requirements
What you’ll bring to the role:
• B. Pharm/M. Pharm/M.Sc. from reputed institute
• 5-10 years, preferably in oral solid Dosage.
• Collaborating across boundaries Functional Breadth with min 3-5 years’ experience in Quality assurance of Pharma/Manufacturing sector such as analytical lab, Manufacturing, engineering in a GMP environment/equivalent.
• Qualification activities, Vendor management Investigation, QMS, Audit, Quality Control & Other GMP activities.
• Quality decision making, Knowledge of IT Applications & tools, Knowledge of TQM and related industry. GxP standards and processes
