Job Description
Amneal Pharmaceuticals is hiring experienced professionals for the role of QA Validation for its pharmaceutical quality assurance and validation operations at the SEZ Matoda facility in Vadodara, Gujarat, India. This full-time opportunity is ideal for candidates with 3 to 9 years of experience in pharmaceutical quality assurance, validation activities, qualification systems, GMP compliance, documentation management, process validation, equipment qualification, cleaning validation, quality systems, and regulated pharmaceutical operations. This position is part of the SEZ Matoda walk-in recruitment drive organized by the company.
The selected candidate will support validation and quality assurance activities associated with pharmaceutical manufacturing operations and compliance systems. Responsibilities include preparing and reviewing validation protocols and reports, supporting equipment qualification and process validation activities, coordinating cleaning validation and qualification documentation, ensuring adherence to GMP guidelines and quality procedures, maintaining validation records and compliance documentation, participating in audit preparation and inspection readiness activities, coordinating with engineering, production, and quality control teams for validation execution, assisting in deviation management and corrective action implementation, monitoring operational compliance standards, and supporting continuous improvement initiatives related to pharmaceutical quality systems and validation operations. Candidates should possess strong understanding of validation practices and regulatory quality systems within pharmaceutical environments.
This role provides valuable exposure to pharmaceutical validation systems, quality assurance operations, GMP regulated environments, compliance documentation systems, equipment qualification activities, and pharmaceutical manufacturing processes within a reputed pharmaceutical organization. Professionals interested in pharmaceutical validation and quality assurance careers can strengthen their compliance and operational expertise through this opportunity.
Location
Vadodara, Gujarat, India
Employment Type
Full-time
Experience Required
3 to 9
Walk-in Interview Details
Walk-in Date: 2026-05-24
About Amneal Pharmaceuticals
Amneal Pharmaceuticals operates in the pharmaceutical industry specializing in formulation manufacturing, quality assurance systems, validation operations, and regulated pharmaceutical products.
Key Responsibilities
Prepare and review validation protocols and reports.
Support equipment qualification and process validation.
Coordinate cleaning validation activities.
Maintain validation records and compliance documentation.
Ensure adherence to GMP and quality procedures.
Participate in audit and inspection readiness activities.
Coordinate with engineering and production teams.
Support deviation handling and CAPA implementation.
Monitor operational quality and compliance systems.
Support continuous improvement in validation operations.
Required Skills
Knowledge of pharmaceutical validation systems.
Understanding of GMP and quality assurance operations.
Awareness of equipment qualification and validation practices.
Documentation and compliance expertise.
Problem-solving and analytical abilities.
Communication and coordination skills.
Time management and workflow planning.
Attention to quality accuracy and compliance.
Adaptability to regulated pharmaceutical environments.
Technical understanding of pharmaceutical quality systems.
Educational Qualification
M.Sc
Industry
Pharmaceutical
Why Join Amneal Pharmaceuticals?
Amneal Pharmaceuticals offers professionals opportunities to work in advanced pharmaceutical validation and quality assurance systems with exposure to regulated GMP manufacturing operations.
How to Apply
Interested candidates can attend the walk-in interview and apply through ACKJOBS for this pharmaceutical validation opportunity.
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