Role Objective
To supervise and coordinate sterile formulation production activities ensuring timely execution of batches with adherence to quality and regulatory requirements.
Key Responsibilities
- Plan and execute batch manufacturing of injectables.
- Supervise machine operators and ensure compliance with SOPs.
- Review and verify batch manufacturing records (BMRs).
- Ensure line clearance and readiness of equipment before operations.
- Monitor environmental conditions and aseptic practices.
- Coordinate with QA QC and engineering for smooth production flow.
- Handle deviations change controls and CAPA implementation.
- Support regulatory audits and inspections.
Qualifications
- /
- 2–9 years of experience in sterile formulation production.
- Strong knowledge of cGMP WHO EU and USFDA guidelines.
Desired Skills
- Leadership and team supervision.
- Strong documentation and compliance orientation.
- Problem-solving and cross-functional collaboration.
Role ObjectiveTo supervise and coordinate sterile formulation production activities ensuring timely execution of batches with adherence to quality and regulatory requirements. Key ResponsibilitiesPlan and execute batch manufacturing of injectables.Supervise machine operators and ensure compliance wi...
Role Objective
To supervise and coordinate sterile formulation production activities ensuring timely execution of batches with adherence to quality and regulatory requirements.
Key Responsibilities
- Plan and execute batch manufacturing of injectables.
- Supervise machine operators and ensure compliance with SOPs.
- Review and verify batch manufacturing records (BMRs).
- Ensure line clearance and readiness of equipment before operations.
- Monitor environmental conditions and aseptic practices.
- Coordinate with QA QC and engineering for smooth production flow.
- Handle deviations change controls and CAPA implementation.
- Support regulatory audits and inspections.
Qualifications
- /
- 2–9 years of experience in sterile formulation production.
- Strong knowledge of cGMP WHO EU and USFDA guidelines.
Desired Skills
- Leadership and team supervision.
- Strong documentation and compliance orientation.
- Problem-solving and cross-functional collaboration.
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