Walk-in | ADL Officer

Ciron Drugs & Pharmaceuticals; Navi Mumbai; On-site; INR 350,000 - 500,000; Full time

Job summary

Ciron Drugs & Pharmaceuticals is seeking an experienced ADL Officer in Navi Mumbai with 2–6 years in pharmaceutical formulation analysis, preferably in an R&D setting. You will perform analytical testing of formulations, support method development and validation, and maintain precise documentation.

Responsibilities include handling HPLC, GC, UV-Vis spectrophotometry and dissolution testing, reviewing reports, protocols, and specifications, and ensuring GLP/GMP compliance and data integrity while

Qualifications

• 2–6 years of experience in pharmaceutical formulation analysis.
• Experience in an R&D environment preferred.
• Strong knowledge of analytical testing regulations and documentation.

Responsibilities

• Perform analytical testing of pharmaceutical formulations, including tablets, capsules, and other dosage forms.
• Handle analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, and dissolution apparatus.
• Conduct analysis of formulation development batches, stability samples, and finished products.
• Support analytical method development, method validation, and method transfer activities.
• Perform dissolution, assay, related substances, and content uniformity testing, as applicable.
• Prepare and review analytical reports, protocols, specifications, and laboratory records.
• Ensure compliance with GLP, GMP, data integrity, and laboratory safety requirements.
• Coordinate with Formulation Development and other R&D teams for analytical requirements.

Skills

Analytical testing

Quality documentation

GLP/GMP knowledge

Team coordination

Tools

HPLC

GC

UV-Vis spectrophotometer

Dissolution apparatus

Job description

Job Summary

We are looking for an experienced ADL Officer with 2 to 6 years of experience in pharmaceutical formulation analysis, preferably in R&D. The candidate will be responsible for analytical testing of pharmaceutical formulations, method development and validation support, and maintaining accurate analytical documentation.

Only Male Candidate should apply.

Key Responsibilities

• Perform analytical testing of pharmaceutical formulations, including tablets, capsules, and other dosage forms.
• Handle analytical instruments such as HPLC, GC, UV-Visible Spectrophotometer, and dissolution apparatus.
• Conduct analysis of formulation development batches, stability samples, and finished products.
• Support analytical method development, method validation, and method transfer activities.
• Perform dissolution, assay, related substances, and content uniformity testing, as applicable.
• Prepare and review analytical reports, protocols, specifications, and laboratory records.
• Ensure compliance with GLP, GMP, data integrity, and laboratory safety requirements.
• Coordinate with Formulation Development and other R&D teams for analytical requirements.