Novartis Hiring 2023.Novartis Notification full details below..Interested and eligible candidates can Apply Now.Our purpose is to reimagine medicine to improve and extend people’s lives. We use innovative science and technology to address some of society’s most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. We also aim to reward those who invest their money, time and ideas in our company.
Vacancy details:
- Post Name: Executive Quality Control (Chemical)
- Qualification: M.Sc. in Chemicals /M. Pharm from reputed university.
- Experienced: 3-7 years, Preferably in Oncology Quality control.
Job Description: Greeting from Novartis !!!!!
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
With 64 manufacturing sites in 26 countries, our aspiration is to become the top manufacturer of innovative and generic medicines in the industry.
Position Purpose:
This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods, and current Compendia at Oncology Kalwe Site.
Your key responsibilities:
Your responsibilities include, but are not limited to:
• Sample storage and management. Analytical testing/documentation of drug product / finished product / complaints / stability / packaging material samples to GxP standards. Stability Testing/Sample storage and management. Analytical documentation of stability samples to GxP standards.
• Analysis of registration batches for tablet & capsule of semi-finished goods/Finished goods in accordance with Quality Control system and cGMP. Analysis of In-process samples and hold time study analysis of intermediate & final drug products.
• Analyst should have exposure for handling of Oncology product for drug substance & drug products. Analysis of raw material (Oncology-API/Excipients) as per current pharmacopoeia and in-house testing procedure and specification.. Analysis of water sample as per current pharmacopoeia. Analysis of cleaning verification/ validation samples.
• Having knowledge about analytical method transfer and perform analytical method transfer for drug substance & drug product. Experience on handling of Quality control instruments like HPLC, Gas chromatography software preferably for empower, dissolution tester, etc.
• Analysis of packaging material (Primary, Secondary & tertiary) as per current pharmacopoeia and current in-house testing procedure and specification. ave knowledge handling the Oncology product.
• To perform internal calibration of instruments. Timely submission of documents pertaining to day-to-day analysis to reviewer. Ensure safe working conditions as per guidelines issued by HSE department. Follow standard operating procedure of Quality control & analysis.
• Ensure Data Integrity, cGMP, GDP, ALCOA and ALCOA+ Principle at Workplace. Assisting supervisor Quality Control for efficient functioning of Quality Control Laboratory through QC analysis and good documentation as per quality control system. . To maintain all testing records, raw data & log books as per SOP
• Maintain confidentiality and ensure safe custody and efficient handling of company document / material. Perform any other task that may be assigned for running of the company as per latest quality standard and Novartis Corporate Guidelines. Ensure efficient inter and intra department communications. Any other responsibility that may be assigned by supervisor/Manager from time to time. Follow Quality behaviors.
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