Position : AM/Manager - Production Injectable
Role & responsibilities:
- Production Oversight: Supervise aseptic manufacturing batch execution and lyophilization .
- Compliance & Documentation: Ensure adherence to cGMP SOPs and regulatory guidelines; review BMRs deviations and CAPAs.
- Resource Management: Plan manpower materials and equipment utilization for smooth operations.
- Technical Leadership: Lead process validations equipment qualifications and technology transfers.
- Cross-Functional Coordination: Collaborate with QA QC Engineering Warehouse and R&D for seamless production.
- Continuous Improvement: Implement process optimization efficiency initiatives and aseptic best practices.
- Audit Readiness: Prepare for internal/external audits and regulatory inspections.
Qualifications
- Graduate/Postgraduate in Pharmacy Biotechnology or related field.
- 7-15 years of experience in sterile injectable production (depending on Manager/AM level).
- Strong knowledge of aseptic techniques regulatory compliance and sterile facility operations.
- Leadership problem-solving and cross-functional collaboration skills.
Position : AM/Manager - Production Injectable Role & responsibilities: Production Oversight: Supervise aseptic manufacturing batch execution and lyophilization .Compliance & Documentation: Ensure adherence to cGMP SOPs and regulatory guidelines; review BMRs deviations and CAPAs.Resource Management: ...
Position : AM/Manager - Production Injectable
Role & responsibilities:
- Production Oversight: Supervise aseptic manufacturing batch execution and lyophilization .
- Compliance & Documentation: Ensure adherence to cGMP SOPs and regulatory guidelines; review BMRs deviations and CAPAs.
- Resource Management: Plan manpower materials and equipment utilization for smooth operations.
- Technical Leadership: Lead process validations equipment qualifications and technology transfers.
- Cross-Functional Coordination: Collaborate with QA QC Engineering Warehouse and R&D for seamless production.
- Continuous Improvement: Implement process optimization efficiency initiatives and aseptic best practices.
- Audit Readiness: Prepare for internal/external audits and regulatory inspections.
Qualifications
- Graduate/Postgraduate in Pharmacy Biotechnology or related field.
- 7-15 years of experience in sterile injectable production (depending on Manager/AM level).
- Strong knowledge of aseptic techniques regulatory compliance and sterile facility operations.
- Leadership problem-solving and cross-functional collaboration skills.
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