Officer to Senior Executive - QA

Drlogy; Vadodara; On-site; INR 500,000 - 800,000; Full time

Job summary

Drlogy is looking for an experienced Officer to Senior Executive in QA responsible for monitoring pharmaceutical manufacturing operations. The role ensures GMP compliance and maintains quality management systems within regulated environments.

Candidates should possess skills in documentation review and line clearance while contributing to quality support. The successful applicant will be involved in ensuring product quality standards and supporting continuous improvement efforts.

Qualifications

• Experience in pharmaceutical quality assurance and compliance monitoring.
• Skilled in documentation review and line clearance.
• Proven ability to support CAPA implementations and audits.

Responsibilities

• Monitor manufacturing operations for GMP compliance consistently.
• Conduct line clearance before production and packaging activities.
• Review batch manufacturing and packaging records accurately.
• Perform in-process quality assurance checks regularly.
• Ensure adherence to SOPs and pharmaceutical quality standards.

Job description

Experienced Officer to Senior Executive - QA responsible for monitoring pharmaceutical manufacturing operations, ensuring GMP compliance, and maintaining quality management systems within regulated environments. Skilled in documentation review, line clearance, deviation handling, audit coordination, and compliance monitoring. Adept at maintaining product quality standards and supporting continuous improvement initiatives.

Responsibilities

• Monitor manufacturing operations for GMP compliance consistently.
• Conduct line clearance before production and packaging activities.
• Review batch manufacturing and packaging records accurately.
• Perform in-process quality assurance checks regularly.
• Ensure adherence to SOPs and pharmaceutical quality standards.
• Investigate deviations and support CAPA implementation activities.
• Coordinate with production and QC teams for quality support.
• Maintain QA documentation and compliance records effectively.
• Monitor environmental and operational compliance standards.
• Participate in audits and regulatory inspection activities.
• Verify equipment cleaning and production readiness procedures.
• Conduct GMP and quality awareness training sessions.
• Support change control and risk assessment activities.
• Ensure compliance with safety and operational procedures.
• Contribute to continuous improvement and quality enhancement initiatives.