Urgent Hiring | Executive- Analytical Method Development (Navi Mumbai)

Marksans Pharma; Navi Mumbai; On-site; INR 600,000 - 900,000; Full time

Job summary

Marksans Pharma Ltd R&D Navi Mumbai is seeking a candidate with 3–8 years of experience in Analytical Method Development to lead method development and validation activities for drug substances and dosage forms. The role requires hands-on use of HPLC, GC, and dissolution techniques, with strong regulatory knowledge and instrument maintenance experience.

The ideal candidate holds a Master’s in Analytical Chemistry or M.Pharm and will contribute to method validation, dissolution development, and

Qualifications

• 2–5 years core experience in Analytical Method Development within a regulated pharmaceutical company.
• MSc or M.Pharm in analytical chemistry or related field.
• Familiar with USP/EP/BP/TGA and regulatory guidelines (ICH/EMEA/FDA).

Responsibilities

• Perform analytical method development and routine analysis of drug substances and dosage forms (liquids, tablets, creams, suspensions).
• Conduct partial analytical method validation for liquids and solid dosage forms.
• Operate analytical instruments such as HPLC, GC, and dissolution equipment.
• Perform dissolution development, comparative dissolution and multimedia dissolution with statistical evaluation and reporting.
• Ensure compliance with USP/EP/BP/TGA and current regulatory guidelines.
• Maintain and calibrate lab instruments/equipment; work with chromatography data systems like Empower 3 or Lab Solutions.

Skills

Analytical Method Development

Routine analysis

HPLC

GC

Dissolution

Empower 3

Education

M.Sc. in Analytical Chemistry

M.Pharm

Tools

Empower 3

Lab Solutions

Job description

Urgent Requirement of 3-8 Years of experience candidate in Analytical Method Development at Marksans Pharma Ltd R & D Navi Mumbai.

Job Responsibilities:

• To perform activities Analytical method development and routine analysis of the of drug substance and liquid, tablets, cream, suspension dosage forms.
• To perform partial Analytical Method validation of liquid, tablets, cream, suspension dosage forms.
• Good understanding and hands on experience of Analytical instruments like HPLC, GC and Dissolution.
• Dissolution development, Comparative dissolution and multimedia dissolution and statistical evaluation and report preparation.
• Well versed with USP/EP/BP/TGA and Various current regulatory guidelines(ICH/EMEA/FDA)
• To perform maintenance and calibration of lab instruments /equipment.
• Hands-on experience with chromatography data systems like Empower 3 or Lab Solutions.
• M.Sc. in Analytical Chemistry, M. Pharm or a related field.
• 2 to 5 years of core experience in Analytical Method Development within a regulated pharmaceutical company.