NEW
REF 1905513
4 hours ago | Sharjah | full time
- General
- Location: Sharjah
- Occupancy: full time
- Description
- Documentation and SOPs:
Develop, review, and update Standard Operating Procedures (SOPs) to ensure consistent and compliant operations.
Validation:
Coordinate activities to validate processes, equipment, and systems, ensuring they consistently perform as intended.
Audits and Compliance:
Conduct internal audits to assess compliance with GMP guidelines and prepare for external inspections.
Deviation and CAPA Management:
Investigate deviations from established procedures, determine root causes, and implement effective Corrective and Preventive Actions (CAPAs).
Batch Release:
Exercise final authority for the release of pharmaceutical batches, ensuring they meet quality standards.
Change Control:
Manage the change control process by assessing the impact of changes to materials, equipment, and procedures.
Training:
Oversee training programs to ensure personnel competency in quality-related processes and GMP.
Record Keeping:
Maintain comprehensive and accurate records for data integrity and traceability.
Required Skills
Attention to Detail: Meticulous approach to reviewing documentation and processes.
Analytical Skills: Ability to analyze data, perform root cause analysis, and assess risks.
Communication Skills: Effectively communicate quality issues, objectives, and findings to cross-functional teams and stakeholders.
Organizational Skills: Strong ability to manage multiple tasks, documents, and projects efficiently.
GMP Knowledge: In-depth understanding of GMP and regulatory requirements.
- Requirements
- Experience: 3 years
- Bachelor degree
- CV
- Provisions
- Salary: to be discussed
- Employment visa provided
- Transportation provided
- Housing provided
- Medical insurance provided
- Publisher
- direct employer
- 51 - 200 employees