Quality Control Analyst

Intracin Pharmaceutical Pvt Ltd; Nadiad; On-site; INR 320,000 - 520,000; Full time

Benefits offered by this job

GMP environment

Vet pharma exposure

Analytical training

Career growth

Job summary

Intracin Pharmaceutical Pvt Ltd in Nadiad, Gujarat, is seeking a QC Analyst to join the Quality Control team. You will perform routine analysis of raw materials, in-process, finished products, and stability samples in line with approved specs, pharmacopoeial standards, SOPs and GMP.

The role involves operating and maintaining lab instruments (HPLC, GC, UV-Vis, FTIR, pH meter), documenting results, supporting method validation, investigations of OOS/OOT, and ensuring compliance with GMP/GLP.

Qualifications

• B.Sc./M.Sc. in Chemistry, B.Pharm/M.Pharm, or equivalent qualification.
• Experience in pharmaceutical, veterinary pharmaceutical, API, or formulation manufacturing preferred.
• Candidates with practical knowledge of HPLC/GC preferred.
• Good understanding of GMP, GLP, pharmacopoeial testing, and lab documentation.
• Freshers with relevant analytical laboratory knowledge may also apply.

Responsibilities

• Perform chemical and instrumental analysis of raw materials, in-process samples, finished products, and stability samples.
• Operate and maintain laboratory instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, pH meter, and analytical balances.
• Perform testing as per IP, BP, USP, Ph. Eur. and approved specifications/methods.
• Prepare and standardize reagents, volumetric solutions, mobile phases, and analytical solutions.
• Review analytical results and ensure compliance with approved specifications.
• Maintain analytical worksheets, logbooks, COA, and laboratory records.
• Follow GMP, GLP, SOPs, data integrity, and safety requirements.
• Assist in investigation of OOS, OOT, deviations, and analytical discrepancies.
• Support method validation, method verification, system suitability, and analytical method transfer activities.
• Perform instrument calibration and routine maintenance as per schedule.
• Maintain laboratory housekeeping and proper handling and storage of chemicals and samples.
• Coordinate with Production, QA, R&D, and Regulatory departments when required.
• Participate in internal audits, regulatory inspections, and continuous improvement activities.

Skills

HPLC / GC analytical skills

Wet chemistry

Pharmacopoeial testing

Documentation and data integrity

OOS / OOT investigation awareness

Good laboratory practices

Attention to detail

Teamwork and communication

Education

B.Sc./M.Sc. in Chemistry, B.Pharm/M.Pharm, or equivalent qualification

Job description

Industry: Pharmaceutical / Veterinary Pharmaceutical Manufacturing

Employment Type: Full-time

About the Role

Department: Quality Control (QC)

Location: Nadiad, Gujarat

Industry: Pharmaceutical / Veterinary Pharmaceutical Manufacturing

Employment Type: Full-time

We are looking for a QC Analyst to join our Quality Control team. The candidate will be responsible for performing routine analysis of raw materials, packaging materials, in-process samples, finished products, and stability samples in accordance with approved specifications, pharmacopoeial standards, SOPs, and GMP requirements.

Key Responsibilities

• Perform chemical and instrumental analysis of raw materials, in-process samples, finished products, and stability samples.
• Operate and maintain laboratory instruments such as HPLC, GC, UV-Visible Spectrophotometer, FTIR, pH meter, and analytical balances.
• Perform testing as per IP, BP, USP, Ph. Eur. and approved specifications/methods.
• Prepare and standardize reagents, volumetric solutions, mobile phases, and analytical solutions.
• Review analytical results and ensure compliance with approved specifications.
• Maintain accurate analytical worksheets, logbooks, COA, and laboratory records.
• Follow GMP, GLP, SOPs, data integrity, and safety requirements.
• Assist in investigation of OOS, OOT, deviations, and analytical discrepancies.
• Support method validation, method verification, system suitability, and analytical method transfer activities.
• Perform instrument calibration and routine maintenance as per schedule.
• Maintain laboratory housekeeping and ensure proper handling and storage of chemicals and samples.
• Coordinate with Production, QA, R&D, and Regulatory departments when required.
• Participate in internal audits, regulatory inspections, and continuous improvement activities.

Required Qualifications

• B.Sc./M.Sc. in Chemistry, B.Pharm/M.Pharm, or equivalent qualification.
• Experience in pharmaceutical, veterinary pharmaceutical, API, or formulation manufacturing will be preferred.
• Candidates with practical knowledge of HPLC/GC will be preferred.
• Good understanding of GMP, GLP, pharmacopoeial testing, and laboratory documentation.
• Freshers with relevant analytical laboratory knowledge may also apply.

Required Skills

• HPLC / GC analytical skills
• Wet chemistry and volumetric analysis
• Pharmacopoeial testing
• Documentation and data integrity
• OOS/OOT investigation awareness
• Good laboratory practices
• Attention to detail
• Teamwork and communication skills

What We Offer

• Opportunity to work in a GMP-compliant pharmaceutical manufacturing environment
• Exposure to veterinary pharmaceutical products and international regulatory requirements
• Learning opportunities in analytical testing, validation, and quality systems
• Professional growth and development opportunities