Research Associate

Simson Pharma; Vasai; On-site; INR 360,000 - 520,000; Full time

Benefits offered by this job

Provident Fund

Job summary

SimSon Pharma Limited is seeking an Analytical Development Laboratory (ADL) Executive to join our Analytical Development team in Vasai, Maharashtra. You will contribute to hands-on pharmaceutical analytical testing, method validation, instrument handling, and GMP/GLP documentation.

The role demands proficiency with HPLC and GC, strong documentation skills, and the ability to support audits and regulatory inspections.

Qualifications

• Hands-on experience in pharmaceutical analytical testing and method validation.
• Knowledge of GMP/GLP compliance and laboratory documentation.
• Ability to draft and review SOPs, CoAs, and analytical reports.

Responsibilities

• Perform analysis of raw materials, intermediates, finished products, and reference standards using validated analytical methods.
• Operate and maintain analytical instruments (HPLC, GC, FTIR, UV-Vis, TLC, etc.) and ensure calibration/verification.
• Prepare reagents, standard solutions, and analytical standards; generate CoAs and lab records.
• Draft, review and update SOPs and analytical documents.
• Investigate deviations, OOS results, and LIRs; support internal and regulatory audits.
• Maintain laboratory inventory and manage procurement for chemicals and consumables.

Skills

HPLC

GC

Analytical testing

Method validation

Documentation

Education

M.Sc. Chemistry

Analytical Chemistry

Pharmaceutical Chemistry

Tools

HPLC

GC

FTIR

UV-Vis

TLC

Refractometer

Humidity Chamber

Muffle Furnace

Job description

Company: SimSon Pharma Limited
Location: Vasai, Maharashtra
Experience: 1-6 Years
Qualification: M.Sc. Chemistry / Analytical Chemistry / Pharmaceutical Chemistry
Employment Type: Full-Time

Job Summary

SimSon Pharma Limited is looking for an experienced Analytical Development Laboratory (ADL) Executive to join our Analytical Development team. The candidate should have hands-on experience in pharmaceutical analytical testing, method validation, instrument handling, laboratory documentation, and GMP/GLP compliance.

Key Responsibilities

• Perform analysis of raw materials, intermediates, finished products, and reference standards using validated analytical methods.
• Operate and maintain analytical instruments including HPLC, GC, FTIR, UV-Visible Spectrophotometer, TLC, Refractometer, Moisture Analyzer, Conductivity Meter, TOC Analyzer, Water Purification System, Vacuum Oven, Water Bath, Muffle Furnace, Humidity Chamber, Magnetic Stirrer, Vacuum Pump, and UV Viewing Cabinet.
• Perform calibration, verification, and routine maintenance of laboratory instruments.
• Execute analytical method verification and method validation activities.
• Prepare and standardize reagents, volumetric solutions, and analytical standards.
• Prepare analytical reports, Certificates of Analysis (CoA), and laboratory records.
• Draft, review, and update Standard Operating Procedures (SOPs) and analytical documents.
• Investigate laboratory deviations, Out-of-Specification (OOS) results, and Laboratory Investigation Reports (LIRs).
• Maintain laboratory inventory and raise Purchase Requisitions (PRs) for chemicals, solvents, glassware, columns, and consumables.
• Ensure compliance with GMP, GLP, data integrity, and internal quality systems.
• Support internal audits, customer audits, and regulatory inspections.

Required Skills

• Strong hands-on experience with HPLC and GC.
• Working knowledge of FTIR, UV, TLC, and other analytical instruments.
• Good understanding of analytical method validation and verification.
• Knowledge of GMP, GLP, ICH guidelines, and laboratory documentation.
• Experience in preparing SOPs, STPs, CoAs, and analytical reports.
• Strong analytical, troubleshooting, and documentation skills.
• Good communication and teamwork abilities.

Preferred Candidate Profile

• 1-6 years of experience in an Analytical Development Laboratory (ADL) in the pharmaceutical industry.
• Ability to independently perform analytical testing and laboratory documentation.
• Exposure to regulatory audits and quality compliance will be an added advantage.

Benefits:

• Provident Fund

Ability to commute/relocate:

• Vasai, Maharashtra (Vasai): Reliably commute or planning to relocate before starting work (Required)

Experience:

• HPLC & GC: 1 year (Required)

Location:

• Vasai, Maharashtra (Vasai) (Preferred)

Work Location: In person