QA Executive - Aseptic Area

Drlogy; Dehradun; On-site; INR 400,000 - 600,000; Full time

Job summary

Drlogy in Dehradun is looking for an Experienced QA Executive for the Aseptic Area. This role involves monitoring sterile manufacturing operations and ensuring compliance with GMP and aseptic processing standards.

The candidate will be responsible for environmental monitoring, documentation review, deviation handling, and maintaining product quality. Skilled individuals with a strong background in sterile production are encouraged to apply.

Qualifications

• Experience in monitoring sterile manufacturing operations.
• Familiarity with GMP and aseptic processing standards.
• Adept in maintaining product quality in sterile production areas.

Responsibilities

• Monitor aseptic manufacturing operations for GMP compliance.
• Conduct line clearance before sterile production activities.
• Ensure compliance with aseptic processing and contamination control procedures.

Skills

Environmental monitoring

Line clearance

Documentation review

Deviation handling

Contamination control

Quality assurance

Job description

Experienced QA Executive - Aseptic Area responsible for monitoring sterile manufacturing operations and ensuring compliance with GMP and aseptic processing standards within pharmaceutical manufacturing environments. Skilled in environmental monitoring, line clearance, documentation review, deviation handling, and contamination control. Adept at maintaining product quality and regulatory compliance in sterile production areas.

• Monitor aseptic manufacturing operations for GMP compliance.
• Conduct line clearance before sterile production activities.
• Ensure compliance with aseptic processing and contamination control procedures.
• Review batch manufacturing and quality documentation accurately.
• Perform in-process quality assurance checks in sterile areas.
• Monitor environmental conditions and cleanroom compliance standards.
• Investigate deviations and support CAPA implementation activities.
• Coordinate with production and microbiology teams for quality support.
• Maintain QA documentation and compliance records effectively.
• Verify equipment cleaning and sterilization procedures regularly.
• Participate in audits and regulatory inspection activities.
• Ensure adherence to SOPs and pharmaceutical quality standards.
• Conduct GMP and aseptic area compliance training sessions.
• Monitor personnel hygiene and gowning practices consistently.
• Contribute to continuous improvement in sterile manufacturing quality systems.