Officer QA

Allrite Group is hiring professionals for the role of Officer – QA for its pharmaceutical quality assurance operations located in Baddi, Himachal Pradesh, India. This full-time opportunity is ideal for candidates with 2 to 5 years of experience in quality assurance operations, GMP compliance workflows, documentation management systems, audit coordination activities, SOP management operations, reporting workflows, and regulated pharmaceutical environments.

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

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

Location

Baddi, Himachal Pradesh, India

Employment Type

Full-time

Salary

₹30,000 – ₹35,000 per month

Experience Required

2 to 5 Years

About Alrite Group

Alrite Group operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, quality workflows, compliance coordination activities, and healthcare product operations.

Key Responsibilities

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

Required Skills

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

Educational Qualification

B.Pharma

Industry

Pharmaceutical

Why Join Alrite Group?

Alrite Group offers professionals opportunities to work in advanced pharmaceutical environments with exposure to quality systems, compliance workflows, operational coordination activities, and healthcare manufacturing operations.