QA Validation Manager – Quality Assurance Validation | Curefox Healthcare | Ahmedabad, Gujarat, India

Curefox Healthcare is seeking an experienced QA Validation Manager to join its pharmaceutical operations in Ahmedabad, Gujarat. This role is designed for professionals who possess strong expertise in pharmaceutical validation processes including equipment validation, process validation, and cleaning validation. The ideal candidate will be responsible for ensuring that manufacturing systems, equipment, and processes meet regulatory compliance requirements. With 4 to 6 years of experience in pharmaceutical quality assurance validation activities, the selected candidate will play an important role in maintaining product quality and regulatory compliance. The QA Validation Manager will collaborate with production, engineering, and quality control teams to ensure that validation protocols are executed effectively and documented accurately. The role requires a deep understanding of GMP guidelines, regulatory documentation, and validation lifecycle management within pharmaceutical manufacturing facilities.

Location

Ahmedabad, Gujarat, India

Employment Type

Full-time

Experience Required

4 to 6

Compensation & Benefits

Competitive salary with opportunities for professional advancement and exposure to pharmaceutical validation processes within a growing healthcare organization.

About Curefox Healthcare

Curefox Healthcare is a pharmaceutical organization dedicated to developing and manufacturing high-quality pharmaceutical formulations. The company focuses on maintaining strict quality assurance standards and regulatory compliance to deliver reliable healthcare solutions.

Position Overview

The QA Validation Manager will oversee validation activities related to pharmaceutical manufacturing equipment, processes, and systems.

Key Responsibilities

• Develop validation protocols and documentation.
• Execute equipment qualification and validation activities.
• Perform process validation and cleaning validation.
• Ensure compliance with GMP and regulatory standards.
• Review validation reports and documentation.
• Coordinate validation activities with cross-functional teams.
• Monitor validation lifecycle and documentation control.
• Participate in internal and external audits.
• Identify and resolve validation-related issues.
• Maintain validation master plans and records.

Required Skills & Competencies

• Strong understanding of pharmaceutical validation processes.
• Knowledge of GMP guidelines and regulatory requirements.
• Experience preparing validation documentation.
• Ability to manage validation lifecycle activities.
• Strong analytical and problem-solving abilities.
• Attention to detail and compliance orientation.
• Experience coordinating with production and engineering teams.
• Strong documentation and reporting skills.

Educational Qualification

Master of Pharmacy (MPharm)

About the Project & Industry

Pharmaceutical validation ensures that manufacturing processes consistently produce products meeting predetermined quality specifications.

Why Join Curefox Healthcare?

Employees gain exposure to quality assurance leadership roles while working in a dynamic pharmaceutical manufacturing environment.

How to Apply

Interested candidates should send their updated resume to: hr@curefox.in