Job Vacancy Hyderabad, Telangana, India Position Expert Science & Technology at Novartis

Major accountabilities:

• Plan, organize, execute, and document scientific experiments (e.g., analytical

  method developments/ validations/ transfers/ stability/ release testing, formulation

  development analytics etc.) according to the agreed timelines and appropriate

  quality standards.

• Accountable for documentation and submission of raw data in appropriate data

  system (for e.g., LIMS test activation and results entry).

• Responsible for good documentation practices (GDP) and good laboratory

  practices (GLP) during execution of laboratory activities.

• Support in evaluation and interpretation of results including investigations on SST failures, OOX/Deviations/Change controls as needed.
• Responsible for assigned laboratory related area/activities (e.g.,

  chemical/reagents/consumables/samples/column/ glassware management etc.).

• Responsible for implementation and maintenance of lean/efficient/environmentally

  sustainable practices in the laboratory.

• Proactively communicate key issues and any other critical topics in a timely manner to the manager and/or to any other relevant project team member(s).
• Responsible to meet KQI (Key quality indicators) and KPI (Key performance

  indicators) for all assigned activities.

• Support internal and external audits and ensure no critical findings within the

  assigned scope.

• Actively contribute to team and organization goals.
• Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISRM & Novartis

  Guidelines.

• Additional specific roles/tasks: See Up4Growth training assignments for the

  business roles for the associate as per the team matrix and completion of trainings in transcript of learning system (e.g., Up4Growth).

Minimum Requirements:

Work Experience:

• Masters in Life Science (e.g., analytical / organic chemistry /pharmacy / pharmaceutical development) or equivalent.
• 5+ years of relevant work experience in OSD forms- hands on in chromatography, multimedia dissolutions, In-vivo & Invitro dissolutions, quality investigations, QBD etc.
• Fluent in English (oral and written).Knowledge of site language, if required.
• Knowledge in quality principles driving drug development such as GMP.
• Understanding of general regulatory and quality expectations.
• Good scientific background, communication skills including presentation and scientific/technical writing.

Skills:

• Environment.
• Experiments Design.
• Health And Safety (Ehs).
• Laboratory Equipment.
• Manufacturing Process.
• Materials Science.
• Process Simulation.
• Project Management.
• Sop (Standard Operating Procedure).
• Technical Writing.

Languages :

• English.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards