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Quality Control Officer

Puerto Lifesciences

Ghiloth, Neemrana, Rajasthan

Department: Quality Control

Experience: 1 Year

Industry: Pharmaceutical

Education: MSC or B.Pharm

Job Description

Quality Control Officer – Quality Control | Puerto Lifesciences | Ghiloth, Neemrana, Rajasthan, India

Puerto Lifesciences is hiring a Quality Control Officer for its pharmaceutical manufacturing facility located in Ghiloth, Neemrana, Rajasthan. This full-time opportunity is ideal for candidates with 1 to 3 years of experience in pharmaceutical quality control operations. The role involves handling analytical testing, documentation, regulatory compliance, and ensuring product quality as per GMP standards. Professionals with hands-on experience in QC laboratory instruments, raw material analysis, finished product testing, and stability studies will find strong career growth in this position. Puerto Lifesciences operates in the pharmaceutical industry with a focus on regulatory-compliant manufacturing and quality-driven processes.

Location

Ghiloth, Neemrana, Rajasthan, India

Employment Type

Full-time

Experience Required

1 to 3 Years

Compensation & Benefits

Salary: Not Disclosed

Industry-standard benefits and professional growth opportunities in pharmaceutical quality operations.

About Puerto Lifesciences

Puerto Lifesciences is a pharmaceutical manufacturing company engaged in the development and production of high-quality formulations. The organization follows GMP-compliant processes and focuses on delivering safe, effective, and regulatory-approved products to domestic and international markets.

Position Overview

The Quality Control Officer will be responsible for conducting laboratory testing, maintaining analytical documentation, ensuring regulatory compliance, and supporting quality systems within the manufacturing unit.

Key Responsibilities

  • Perform analysis of raw materials, in-process samples, and finished products.
  • Operate and maintain laboratory instruments such as HPLC, UV, and dissolution apparatus.
  • Prepare and review analytical reports and documentation.
  • Ensure compliance with GMP, GLP, and regulatory guidelines.
  • Conduct stability studies and maintain related records.
  • Assist in method validation and calibration activities.
  • Monitor environmental and quality control parameters.
  • Support audits and regulatory inspections.
  • Maintain proper laboratory housekeeping and safety standards.

Required Skills & Competencies

  • Knowledge of pharmaceutical quality control procedures.
  • Hands-on experience with analytical laboratory instruments.
  • Understanding of GMP and regulatory compliance standards.
  • Strong documentation and reporting skills.
  • Attention to detail and analytical thinking ability.
  • Good communication and teamwork skills.
  • Ability to handle laboratory equipment efficiently.
  • Problem-solving skills in quality-related issues.

Educational Qualification

M.Sc or B.Pharm

About the Project & Industry

The pharmaceutical manufacturing sector in Rajasthan is expanding rapidly with strong regulatory focus and export potential. This role provides exposure to quality control systems, analytical testing procedures, and regulatory-driven manufacturing environments.

Why Join Puerto Lifesciences?

  • Opportunity to work in a GMP-compliant pharmaceutical facility.
  • Hands-on exposure to analytical quality control systems.
  • Career advancement in pharmaceutical quality operations.
  • Professional and regulatory learning environment.

How to Apply

Interested candidates can send their updated resume to hr@puerto.in. Shortlisted applicants will be contacted for further selection process.

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