Position : Deputy Manager – QA IPQA (Sterile Injectable)
Key Responsibilities
Monitor and control IPQA activities in sterile injectable manufacturing filling and packaging areas.
Ensure adherence to aseptic practices gowning procedures and cleanroom behavior.
Review and approve batch manufacturing records line clearance and critical process steps.
Conduct in-process checks sampling and verification of critical parameters during production.
Supervise environmental monitoring and ensure timely escalation of deviations.
Support investigations CAPA implementation and root cause analysis for quality issues.
Coordinate with production QC and engineering teams to ensure smooth operations.
Assist in audits (regulatory and internal) and ensure compliance readiness.
Train and mentor QA associates on sterile practices and quality systems.
Qualifications & Experience
Bachelor’s/Master’s degree in Pharmacy Biotechnology or related field.
6–10 years of experience in QA/IPQA within sterile injectable manufacturing.
Strong knowledge of aseptic techniques cGMP and regulatory guidelines (USFDA EMA WHO).
Experience in handling audits deviations and CAPA.
Excellent communication documentation and leadership skills.
Position : Deputy Manager – QA IPQA (Sterile Injectable)Key ResponsibilitiesMonitor and control IPQA activities in sterile injectable manufacturing filling and packaging areas.Ensure adherence to aseptic practices gowning procedures and cleanroom behavior.Review and approve batch manufacturing recor...
Position : Deputy Manager – QA IPQA (Sterile Injectable)
Key Responsibilities
Monitor and control IPQA activities in sterile injectable manufacturing filling and packaging areas.
Ensure adherence to aseptic practices gowning procedures and cleanroom behavior.
Review and approve batch manufacturing records line clearance and critical process steps.
Conduct in-process checks sampling and verification of critical parameters during production.
Supervise environmental monitoring and ensure timely escalation of deviations.
Support investigations CAPA implementation and root cause analysis for quality issues.
Coordinate with production QC and engineering teams to ensure smooth operations.
Assist in audits (regulatory and internal) and ensure compliance readiness.
Train and mentor QA associates on sterile practices and quality systems.
Qualifications & Experience
Bachelor’s/Master’s degree in Pharmacy Biotechnology or related field.
6–10 years of experience in QA/IPQA within sterile injectable manufacturing.
Strong knowledge of aseptic techniques cGMP and regulatory guidelines (USFDA EMA WHO).
Experience in handling audits deviations and CAPA.
Excellent communication documentation and leadership skills.
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