Novartis Mumbai Hiring For Quality Control Department
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| Novartis Mumbai Hiring For Quality Control Department |
Novartis Mumbai Job Vacancy Details:
Position: Executive Quality Control
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 Compendial at Kalwe Site.
M.Sc. in Chemicals /M. Pharm from reputed university with min 5+ yrs experience in Quality function.
Sound technical & scientific knowledge of pharmaceutical/ chemical analytics/ QC/ equivalent Working experience in Laboratory environment in the Pharmaceutical industry.
Experience in Laboratory Excellence & Laboratory equipment Quality Control (QC) Testing Quality Control Sampling.
Your key responsibilities:
Your responsibilities include, but are not limited to:
Sample storage and management (FDF & API), 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. Analytical Method Validation & Analytical Method Transfer.
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
Ensure Data Integrity, cGMP, GDP, ALCOA and ALCOA+ Principle at Workplace
Any other responsibility that may be assigned by supervisor/Manager from time to time.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Location: Navi Mumbai, Maharashtra
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 Compendial at Kalwe Site.
Minimum requirements
M.Sc. in Chemicals /M. Pharm from reputed university with min 5+ yrs experience in Quality function.
Sound technical & scientific knowledge of pharmaceutical/ chemical analytics/ QC/ equivalent Working experience in Laboratory environment in the Pharmaceutical industry.
Experience in Laboratory Excellence & Laboratory equipment Quality Control (QC) Testing Quality Control Sampling.
Your key responsibilities:
Your responsibilities include, but are not limited to:
Sample storage and management (FDF & API), 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. Analytical Method Validation & Analytical Method Transfer.
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 Data Integrity, cGMP, GDP, ALCOA and ALCOA+ Principle at Workplace
Any other responsibility that may be assigned by supervisor/Manager from time to time.
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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