Novartis Chemical Quality Control Executive Vacancy – Apply Online
Novartis invited candidates with an MSc chemical science degree for the post of Executive Quality Control (Chemical). chemistry job opening 2021. chemical science job 2021. Executive Quality Control (Chemical) job opening 2021. chemistry job opening 2021. Chemistry job 2021. Check out all the details on rasayanika.
Job Title: Executive Quality Control (Chemical)
Job Id: 324287BR
Minimum requirements
What you’ll bring to the role:
• M.Sc. in Chemicals /M. Pharm from a reputed university.
• 3-7 years, Preferably in Oncology Quality control.
• Sound technical & scientific knowledge of pharmaceutical/ chemical analytics/QC/ equivalent Working experience in Laboratory environment in the Pharmaceutical industry.
• Laboratory Excellence & Laboratory equipment Quality Control (QC) Testing Quality Control Sampling Infrastructure Management Quality decision making.
• Knowledge of TQM and related industry GxP standards and processes.
Job Description
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 the handling of Oncology products for drug substances & drug products. Analysis of raw material (Oncology-API/Excipients) as per current pharmacopeia and in-house testing procedure and specification.. Analysis of water sample as per current pharmacopeia. Analysis of cleaning verification/ validation samples.
• Having knowledge about analytical method transfer and perform analytical method transfer for drug substance & drug product. Experience on the handling of Quality control instruments like HPLC, Gas chromatography software preferably for empowering, dissolution tester, etc.
• Analysis of packaging material (Primary, Secondary & tertiary) as per current pharmacopeia 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 the reviewer. Ensure safe working conditions as per guidelines issued by HSE department. Follow the standard operating procedure of Quality control & analysis.
• Ensure Data Integrity, cGMP, GDP, ALCOA, and ALCOA+ Principle at Workplace. Assisting supervisor Quality Control for the efficient functioning of Quality Control Laboratory through QC analysis and good documentation as per quality control system. . To maintain all testing records, raw data & logbooks as per SOP.
• Maintain confidentiality and ensure safe custody and efficient handling of company documents/material. Perform any other task that may be assigned for running of the company as per the 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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