Quality Head – Quality Assurance | Suraj Laboratories | Yadgir, Karnataka, India

Suraj Laboratories is hiring senior professionals for the role of Quality Head for its pharmaceutical manufacturing operations located in Yadgir, Karnataka, India. This full-time opportunity is suitable for candidates with 15 to 20 years of experience in pharmaceutical quality assurance, quality systems management, GMP compliance operations, audit coordination, manufacturing quality control, and leadership roles within pharmaceutical manufacturing environments. This position is aligned with GM/DGM-level responsibilities and requires strong leadership capabilities in managing quality operations and compliance systems. The selected candidate will oversee quality assurance activities, manage pharmaceutical compliance systems, coordinate audits and quality reviews, maintain quality documentation, and ensure adherence to regulatory and operational standards across manufacturing facilities. Candidates having expertise in pharmaceutical quality systems, regulatory compliance management, audit handling, manufacturing quality operations, and team leadership will be preferred. This role offers valuable exposure to advanced pharmaceutical quality systems, leadership operations, regulatory coordination environments, and manufacturing practices focused on compliance excellence, operational quality, regulatory readiness, and continuous improvement.

Location

Yadgir, Karnataka, India

Employment Type

Full-time

Experience Required

15 to 20

Compensation & Benefits

Competitive salary package with pharmaceutical quality leadership exposure, regulatory management experience, and long-term professional growth opportunities.

About Suraj Laboratories

Suraj Laboratories operates in the pharmaceutical industry specializing in API manufacturing systems, pharmaceutical production operations, and regulated healthcare environments.

Position Overview

The Quality Head will oversee pharmaceutical quality assurance systems, compliance operations, and manufacturing quality coordination activities.

Key Responsibilities

• Manage pharmaceutical quality assurance and compliance operations.
• Coordinate audit preparation and regulatory quality systems.
• Maintain quality documentation and compliance records.
• Monitor manufacturing quality standards and operational systems.
• Ensure adherence to GMP and pharmaceutical regulations.
• Coordinate with production, engineering, and regulatory teams.
• Participate in quality review and management meetings.
• Support continuous improvement and compliance enhancement activities.
• Monitor operational discipline within quality systems.
• Lead quality teams and manufacturing compliance operations.

Required Skills & Competencies

• Strong understanding of pharmaceutical quality assurance systems.
• Knowledge of GMP compliance and regulatory operations.
• Leadership and team management abilities.
• Problem-solving and analytical thinking capabilities.
• Awareness of pharmaceutical manufacturing standards.
• Ability to manage quality workflows efficiently.
• Attention to compliance accuracy and operational quality.
• Communication and audit coordination capabilities.
• Time management and multitasking skills.
• Adaptability to regulated pharmaceutical environments.

Educational Qualification

MPharm

About the Project & Industry

The pharmaceutical manufacturing industry depends on strong quality systems, regulatory compliance practices, and operational excellence to support safe healthcare production and regulatory approvals.

Why Join Suraj Laboratories?

Suraj Laboratories offers opportunities to work in advanced pharmaceutical manufacturing environments with exposure to leadership-level quality systems and compliance operations.

How to Apply

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