Associate Scientist - Technical Development

Haridwarbn; Hyderabad; On-site; INR 700,000 - 1,100,000; Full time

Job summary

Novartis India in Hyderabad invites an Associate Scientist - Technical Development to plan and perform scientific experiments for DS/DP development within a multifunctional project team led by a Project Leader.

You will maintain lab instruments, ensure GDP/GLP compliance, contribute to method development, validation, transfer and data documentation, and support investigations of deviations and changes.

Qualifications

• Strong expertise in Chromatography and Dissolution Testing.
• Experience in Analytical Method Development, Validation, and Transfer.
• Knowledge of Regulatory Compliance and GLP standards.
• M.Pharm./M.Sc. with 2–5 years in a related domain.
• Proficiency with GDP/GLP documentation and data handling.

Responsibilities

• Plan, perform and document laboratory experiments for DS/DP in cross‑functional teams.
• Maintain lab instruments and day‑to‑day operations.
• Execute experiments to meet timelines and quality standards.
• Ensure GDP/GLP documentation and data management.
• Support investigations on SST failures, deviations, and change controls.

Skills

Chromatography

Dissolution Testing

Analytical Method Development

Validation

Regulatory Compliance

Laboratory Equipment

Manufacturing Process

Process Simulation

GLP standards

Materials Science

Education

M.Pharm./M.Sc. with 2-5 years experience

Tools

GLIMS

Chromeleon

ELN

Job description

# Associate Scientist - Technical DevelopmentNovartis India2 months ago* Job Details* Key Skills* Recruiter Details* Company Details#### Key Highlights* 2 to 6 Yrs* Not Disclosed* Hyderabad##### Job DescriptionAssoc. Scientist - Technical Development Job Description Summary -Plan and perform scientific experiments (or pilot plant processes) for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures in collaboration within a multifunctional project team coordinated by a Project leader. Contribute to maintenance of lab instruments/infrastructure. -SANDOZ: Plan and perform scientific experiments (or pilot plant processes) for the development and timely delivery of drug products (DP), processes and procedures in collaboration within a multifunctional project team coordinated by a Project leader. Contribute to maintenance of lab instruments/infrastructure. -Support development projects aiming the development of stable, bioequivalent, robust and cost competitive dosage forms -Design and manage experiments/batches for simple/low complexity products under supervision, provide related scientific documentation -Plan and execute experiments in agreement with quality risk management and GDevP /GMP -Assists in the preparation of and reviews of the technological part of dossier Job Description Key Responsibilities Plan, perform and document scientific experiments in the laboratory for drug substances (DS) and drug products (DP) in collaboration with multifunctional project teams. Contribute to maintenance of lab instruments/day-to-day operations. Timely execution of project related activities. 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). Accountable 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 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. Essential Requirements: Strong expertise in Chromatography and Dissolution Testing, including method selection and handling Proven experience in Analytical Method Development, Validation, and Transfer Solid understanding of Regulatory Compliance and GLP standards M.Pharm./M.Sc. with up to 2 -5 years of relevant experience, with demonstrated experience in a related domain. Desirable Requirements: Understanding digital tools Hands on experience with GLIMS, Chromeleon and ELN Skills Desired Environment, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure) .###### Other Details* Industry**Medical / Healthcare*** Recruiter Details**Novartis India*** Job Type**Full time**SKILLS* Chromatography* Dissolution Testing* Analytical Method Development* Validation* Regulatory Compliance* Laboratory Equipment* Manufacturing Process* Process Simulation* GLP standards* Materials Science