Senior Executive : Research & Development

Geltec Private Limited; Bengaluru; On-site; INR 900,000 - 1,200,000; Full time

Job summary

Geltec Private Limited in Bengaluru seeks a scientist with 2-6 years in pharma to lead analytical development activities. You will operate HPLC, GC, UV, IR, and dissolution instruments, develop and validate methods, and prepare protocols and reports. Knowledge of GMP/GLP/GDP and regulatory guidelines is essential.

The role emphasizes cross-functional collaboration and stability studies, with a focus on quality and compliance in a regulated environment.

Qualifications

• 2-6 years in Pharmaceutical industry.
• M.Sc. in Chemistry with relevant analytical experience.
• Experience in analytical development, method validation and regulatory alignment.

Responsibilities

• Handle analytical instruments like HPLC, GC, UV, IR, Autotitrator and dissolution apparatus.
• Develop and optimize analytical methods.
• Validate methods for assay, dissolution and related substances per regulatory requirements.
• Prepare validation protocols and reports.
• Troubleshoot analytical instruments.
• Gain experience in stability studies and regulatory expectations.
• Ensure quality and compliance per GMP/GLP/GDP.

Skills

Analytical method development

Method validation

Cross-functional collaboration

Quality & GMP/GLP/GDP knowledge

Regulatory & ICH guidelines

Troubleshooting analytical instruments

Stability studies

Pharmacopeial knowledge

Education

M.Sc. in Chemistry

Tools

HPLC

GC

UV

IR

Autotitrator

Dissolution apparatus

Job description

Core requirements

• Work Experience: 2- 6 years in Pharmaceutical industry


• Education: M.Sc. in Chemistry


• Department: Analytical development

Key Responsibilities

• Candidate should know handling of analytical instruments like HPLC, GC, UV, IR, Autotitrator, Dissolution apparatus and other basic analytical instruments.


• Candidate should be well versed with Analytical method development & method optimization


• Candidate should be well versed with Analytical method Validation for Assay, Dissolution and Related substances as per regulated market requirements.


• Candidate should know preparation of method validation protocols and reports.


• Candidate should know analytical instruments trouble shooting.


• Should have experience on stability studies and requirements.


• Should have fair knowledge of Regulatory requirements and ICH guidelines.


• Should have good Cross-functional collaboration


• Candidate should have knowledge on Quality & compliance in GMP/GLP/GDP


• Should have basic technical Competencies on Pharmacopeial and guideline requirements.