Assistant Manager Validation

Symbiotec Zenfold Pvt. Ltd. is hiring experienced professionals for the role of Assistant Manager – Qualification & Validation for its pharmaceutical validation and quality operations located in Ujjain, Madhya Pradesh, India. This full-time opportunity is ideal for candidates with 5 to 10 years of experience in qualification operations, validation workflows, GMP compliance systems, documentation management activities, audit coordination workflows, reporting systems, and regulated pharmaceutical environments.

The selected candidate will support qualification and validation coordination activities associated with pharmaceutical manufacturing systems and operational workflows. Responsibilities include handling equipment qualification and validation activities, maintaining validation records and technical documentation, coordinating with QA and production teams for operational support activities, monitoring validation systems and qualification workflows, ensuring adherence to GMP procedures and quality standards, preparing validation reports and operational documentation, assisting in troubleshooting and validation coordination workflows, participating in audit review and compliance activities, supporting validation management systems, and maintaining continuous improvement of validation operations and compliance efficiency.

This role offers valuable exposure to pharmaceutical validation systems, compliance workflows, documentation coordination activities, technical documentation systems, qualification operations, and regulated pharmaceutical environments within a reputed organization. Professionals interested in validation and quality assurance careers can strengthen their technical and operational expertise through this opportunity.

Location

Ujjain, Madhya Pradesh, India

Employment Type

Full-time

Salary

Best in Industry

Experience Required

5 to 10 Years

About Symbiotec Pharmalab Pvt. Ltd.

Symbiotec Pharmalab Pvt. Ltd. operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, validation workflows, compliance coordination activities, and healthcare product operations.

Key Responsibilities

• Support qualification and validation activities.
• Maintain validation records and technical documentation.
• Coordinate with QA and production teams.
• Monitor validation systems and qualification workflows.
• Ensure adherence to GMP procedures and quality standards.
• Prepare validation reports and operational documentation.
• Support troubleshooting and validation coordination workflows.
• Participate in audit review and compliance activities.
• Assist in qualification and compliance coordination activities.
• Support continuous improvement of validation systems.

Required Skills

• Strong knowledge of qualification and validation operations.
• Understanding of GMP workflows and pharmaceutical systems.
• Knowledge of compliance coordination and validation activities.
• Experience in documentation and reporting systems.
• Good analytical and problem-solving abilities.
• Strong communication and teamwork skills.
• Knowledge of pharmaceutical standards and validation systems.
• Ability to manage validation schedules and workflows.
• Attention to documentation accuracy and compliance standards.
• Adaptability to regulated pharmaceutical environments.

Educational Qualification

B.Pharma

Industry

Pharmaceutical

Why Join Symbiotec Pharmalab Pvt. Ltd.?

Symbiotec Pharmalab Pvt. Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to validation systems, compliance workflows, operational coordination activities, and healthcare manufacturing operations.