QA Senior Executive or Assistant Manager

Drlogy; Dehradun; On-site; INR 600,000 - 800,000; Full time

Job summary

Drlogy in Dehradun is looking for an experienced QA Senior Executive or Assistant Manager to manage pharmaceutical quality assurance operations. You will supervise compliance activities, ensure adherence to GMP standards, and conduct audits.

The ideal candidate should have a solid background in audit management, documentation control, and CAPA handling. This role is crucial for maintaining quality standards and supporting regulatory compliance initiatives.

Qualifications

• Minimum 3 years of experience in pharmaceutical quality assurance.
• Strong understanding of GMP and quality management systems.
• Proven track record in audit management and compliance.

Responsibilities

• Supervise quality assurance operations and compliance activities.
• Ensure adherence to GMP and pharmaceutical quality standards.
• Conduct internal audits and support regulatory inspections.

Skills

Audit management

Documentation control

CAPA handling

Compliance monitoring

Team coordination

Job description

QA Senior Executive or Assistant Manager

Experienced QA Senior Executive or Assistant Manager responsible for managing pharmaceutical quality assurance operations, ensuring GMP compliance, and supervising quality systems within manufacturing environments. Skilled in audit management, documentation control, CAPA handling, compliance monitoring, and team coordination. Adept at maintaining product quality standards and supporting regulatory compliance initiatives.

• Supervise quality assurance operations and compliance activities.
• Ensure adherence to GMP and pharmaceutical quality standards.
• Review batch manufacturing records and quality documentation accurately.
• Coordinate deviation, CAPA, and change control processes effectively.
• Conduct internal audits and support regulatory inspections.
• Monitor implementation of quality systems across departments.
• Coordinate with QC, production, and regulatory teams efficiently.
• Investigate quality incidents and implement corrective actions.
• Maintain QA records and compliance databases systematically.
• Conduct GMP and compliance training programs for staff.
• Monitor quality KPIs and operational performance metrics.
• Support risk assessment and quality improvement initiatives.
• Ensure timely closure of audit observations and deviations.
• Maintain audit readiness and regulatory compliance standards.
• Contribute to operational excellence and continuous improvement programs.