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 Compendial at Kalwe Site.

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:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum requirements
What you\xe2\x80\x99ll bring to the role:

• 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.

Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse team\xe2\x80\x99s representative of the patients and communities we serve.

Join our Novartis Group Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

Why Sandoz?
500 million patients were touched by Sandoz generic and biosimilar medicines in 2021 and while we\xe2\x80\x99re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world.

How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what\'s possible, when we collaborate with courage to aggressively and ambitiously tackle the world\xe2\x80\x99s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!

Imagine what you could do here at Sandoz!
Division
Novartis Technical Operations
Business Unit
QUALITY
Country
India
Work Location
Mumbai
Company/Legal Entity
Sdz Pvt Ind
Functional Area
Quality
Job Type
Full Time
Employment Type
Regular
Shift Work
No
Early Talent
No