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Quality Assurance Officer

West Coast Pharmaceutical Works Limited

Vadaswami, Gandhinagar, Gujarat

Department: Quality Assurance

Experience: 0-2 Years

Industry: Pharmaceutical

Education: BSc MSc

Job Description

Quality Assurance Officer – Quality Assurance | West Coast Pharmaceutical Works Limited | Gandhinagar, Gujarat, India

West Coast Pharmaceutical Works Limited is inviting applications for the position of Quality Assurance Officer at its pharmaceutical manufacturing facility in Vadaswami, Gandhinagar, Gujarat, India. This full-time opportunity is suitable for candidates with 0 to 2 experience who are interested in building a career in quality assurance within the Pharmaceutical industry in India. The role involves ensuring compliance with Good Manufacturing Practices (GMP), reviewing batch documentation, supporting validation processes, and maintaining quality standards during pharmaceutical manufacturing operations. The selected candidate will work closely with production, quality control, and regulatory teams to ensure products meet required quality specifications and regulatory guidelines. The position offers valuable exposure to pharmaceutical quality systems, regulatory compliance procedures, and manufacturing documentation processes in a regulated pharmaceutical production environment.

Location

Gandhinagar, Gujarat, India

Employment Type

Full-time

Experience Required

0 to 2

Compensation & Benefits

Salary range: 0 to 2 with opportunities to gain experience in pharmaceutical quality systems, regulatory compliance, and manufacturing quality assurance operations.

About West Coast Pharmaceutical Works Limited

West Coast Pharmaceutical Works Limited is a well-established pharmaceutical company involved in manufacturing high-quality pharmaceutical formulations and healthcare products for domestic and international markets.

Position Overview

The Quality Assurance Officer will support pharmaceutical quality management systems by ensuring compliance with GMP standards, reviewing manufacturing documentation, and maintaining regulatory compliance.

Key Responsibilities

  • Review batch manufacturing and packaging records.
  • Ensure compliance with GMP and quality standards.
  • Assist in validation and qualification activities.
  • Maintain documentation for quality assurance processes.
  • Coordinate with production and quality control teams.
  • Support internal and external quality audits.
  • Monitor compliance with standard operating procedures.
  • Investigate deviations and support corrective actions.
  • Ensure proper documentation and record management.
  • Support continuous improvement in quality systems.

Required Skills & Competencies

  • Knowledge of pharmaceutical quality assurance systems.
  • Understanding of GMP guidelines.
  • Documentation and record management skills.
  • Attention to detail in quality processes.
  • Communication and coordination skills.
  • Problem-solving capability.
  • Ability to work in regulated manufacturing environments.
  • Analytical thinking ability.
  • Team collaboration skills.

Educational Qualification

BSc MSc

About the Project & Industry

This role supports pharmaceutical formulation manufacturing and quality management systems within regulated pharmaceutical production facilities.

Why Join West Coast Pharmaceutical Works Limited?

Opportunity to build a career in pharmaceutical quality assurance while working in a regulated manufacturing environment focused on high-quality medicine production.

How to Apply

hr.va@westcoastin.com
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